Latest revision as of 03:14, 20 October 2016

Labjournal

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Samples

Transformation of E. coli XL1 blue with Phytochrome B (2–908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Rosario

Aim of the experiment: Transformation of Phytochrome B for protein fusion

Procedure:

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

2 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 45 min at 37 °C in the 180 rpm cell-culture shaker

100 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 100 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.

Miniprep of pTUM100 with pGAL, pTEF1, pTEF2, pADH and RFC25 compatible RFP generator

Investigator: Jeff, Rosario

Aim of the experiment: Miniprep of pTUM100 with pGAL, pTEF1, pTEF2, pADH and RFC25 compatible RFP generator

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Sequencing of RFP-Generator (RFC25, pSB1C3)

Investigator: Jeff, Rosario

Aim of the experiment: Sequencing of RFP-Generator (RFC25, pSB1C3)

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer)

Picking of of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Rosario, Florian

Aim of the experiment: Picking of of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Procedure:

pSB1C3 plasmid with BBa_K801031 (PhyB 2 - 908 aa, RFC25): Colonies were picked from chloramphenicol plates.

Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contain 4 mL of LB-medium + 4 µL chloramphenicol(1000x).

4 colonies were picked.

These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight

Analytical digestion and gelelectrophoresis of RFP-generator (RFC25, pSB1C3, P4 & P5)

Investigator: Jeff, Rosario, Florian

Aim of the experiment: Analytical digestion and gelelectrophoresis of RFP-generator (RFC25, pSB1C3, P4 & P5).

Procedure:

Batch for analytical digestion for P4 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P4
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Batch for analytical digestion for P5 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P5
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Incubation for 90 min at 37 °C.

Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder	P4	P5
	Mutation successful	Mutation successful!

Parts are compliant and do not contain RFC25 forbidden restriction sites.

500px

Sequencing of pTUM vectors with pGAL, pADH, pTEF1, pTEF2

Investigator: Jeff, Rosario, Florian

Aim of the experiment: Sequencing of pTUM vectors with pGAL, pADH, pTEF1, pTEF2

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer).

The different vectors we sequenced received the following barcodes:

- ADH in pTUM100: FR01002265

- TEF1 in pTUM100: FR01002266

- TEF2 in pTUM100: FR01002266

- GAL in pTUM100: FR01002268

Sequencing of TEF2 in pTUM100 was not interpretable. The other sequences were consistent with the sequences in the parts registry.

Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Investigator: Jeff, Florian

Aim of the experiment: Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3).

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10

Investigator: Jeff, Florian

Aim of the experiment: Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10.

Procedure:

Batch for analytical digestion for P7 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P7
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Batch for analytical digestion for P8 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P8
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Batch for analytical digestion for P9 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P9
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Batch for analytical digestion for P10 with NgoMIV+AgeI-HF

volume	reagent
2.5 µl	Plasmid DNA P10
2 µl	NEBuffer 4 (10x)
0.25 µl	NgoMIV (10 U/µl)
0.25 µl	AgeI-HF (20 U/µl)
15 µl	ddH2O
=20 µl	TOTAL

Incubation for 90 min at 37 °C.

Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

1 kbp ladder DNA ladder	P7	P8	P9	P10
	Part is correct	Part is correct	Part is correct	Part is correct

500px

Transformation of E. coli XL1 blue with

Investigator:

Aim of the experiment: Transformation of E. coli XL1 blue.

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of µl LB-medium to each tube.

The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37 °C in the cell-culture shaker.

Week 1, May 16th - May 22nd

Monday, May 16th

Streptavidin Plasmid Check

Investigator: JB, LK, JH

Aim of the experiment: Verify cloning

Procedure:

MiniPrep following manufacturer's protocol (QIAprep MiniPrep, Qiagen) (4 clones each of pSA1, pSAm1 in pASK75)
Analytic digestion with 0.25 µL XbaI, 0.25 µL HindIII (HF), 1 µL SmartCut Buffer, 5 µL plasmid DNA, 3.5 µl H₂O
5 µL analyzed in gel electrophoresis (1% agarose)

Results: Successful cloning verified. Stored at –20 °C

Lane 1: 5 µL Thermo Fisher, 1 kb ladder

Lanes 2–9: 5 µL digestions of P6–P13, band of SA (mut1) at about 300 bp, band of digested plasmid at about 3,000 bp

Streptavidin Expression: Transform BL21

Investigator: JB, JH

Aim of the experiment: Express pSA1 and pSAm1 in E. coli BL21

Procedure:

Transformation into competent E. coli BL21 according to protocol of P6 and P10

Results: Plates (LB Amp) in incubator (37 °C) for further processing

Tuesday, May 17th

SDS Gel Analysis

Investigator: CG

Aim of the experiment: Analyze collagen 1/2, eGFP, fraction 30 of egg precipitation via SDS gel

Procedure:

Mixed 80 µL samples with 20 µL SDS buffer

Heated at 95 °C for 10 min

1 d staining, 1 d unstaining

Results: Successful cloning verified. Stored at –20 °C

Lane 1: 8 µL marker (Thermo Fisher #26610)

Lane 2: Fraction 30 (IEC), 3 µL, band at 35 kDa, avidin expected at 16 kDa

Lane 3: eGFP, 12 µL, band at 27 kDa, eGFP expected at 27 kDa, many impurities

Lane 4: Collagen 1, 12 µL, no sharp band

Lane 5: Collagen 1, 12 µL, no sharp band

$Muc16 SDS gel analysis fraction 30 of egg-precipitation.png$

MiniPreps pSb1C3–AviTag, –A3C5 and pASK75–(SA1), –(SAm1)

Investigator: CR, CG

Aim of the experiment: Verify cloning

Procedure:

MiniPrep was performed following manufacturer's protocol (QIAprep MiniPrep, Qiagen)

Analytic digestion with 0.25 µL XbaI, 0.25 µL HindIII (HF) for pASK plasmids and 0.25 µL NgomIV, 0.25 µL AgeI (HF) for pSb1C3 plasmids, 1 µL SmartCut Buffer, 5 µL plasmid DNA, 3.5 µL H₂O

5 µL on 1% agarose gel electrophoresis

Results: Successful cloning verified for pASK plasmids. Repeat pSb1C3 plasmids. Stored at –20 °C

Lane 1: 5 µL Thermo Fisher, 1 kb Ladder

Lane 2: 5 µL digestion of pSb1C3–AviTag

Lane 3: 5 µL digestion of pSb1C3–A3C5

Lane 5: 5 µL digestion of pASK75(SA1), EB elution

Lane 6: 5 µL digestion of pASK75(SAmut1), EB elution

Lane 7: 5 µL digestion of pASK75(SAmut1), H₂O elution

Inoculation of Pre-Culture with BL21 (pASK75 (SA1)) in LB Medium

Investigator: CR

Aim of the experiment: Pre-culture for streptavidin expression in TB medium

Procedure:

Added 50 µL ampicillin to 50 mL LB medium

Picked colonies from BL21 (pASK75 (SA1))

Inoculated LB medium

Incubated at 30 °C overnight

Wednesday, May 18th

Repeat Analytical Gel of pSb1C3–AviTag, –A3C5

Investigator: CG, CR

Aim of the experiment: Verify cloning

Procedure:

Analytic digestion with 0.25 µL NgoMIV, 0.25 µL AgeI (HF) for pSb1C3 plasmids, 1 µL SmartCut Buffer, 8.5 µL plasmid DNA
10 µL analyzed in gel electrophoresis (2% agarose)

Results:

Inoculation of BL21 (pASK75 (SA1)) Culture in 2 L TB Medium and Induction of Streptavidin Production by Addition of Tetracycline

Investigator: CR

Aim of the experiment: Produce streptavidin

Procedure:

Ampicillin (2 mL) was added to the medium (1:1000)
The pre-culture (50 mL) was poured into the medium
Culture incubated at 37 °C and 140 rpm until OD₅₅₀ reached 0.5
To induce streptavidin expression, anhydro-tetracycline (200 µL) was added to the culture (1:10,000)
The culture was incubated at 37 °C and 140 rpm for 4 hours

Results: Streptavidin expression by BL21

Expression and Harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB Medium

Investigator: CR, JB, JH

Aim of the experiment: Recombinant expression and purification of streptavidin

Procedure:

After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
The supernatant was discarded, and the pellet was transferred into a beaker of sufficient size and resuspended in Tris Buffer B cooled to 4 °C (50 mM Tris/HCl pH = 8.0, 1 mM EDTA)
The solution was homogenized in the PANDA (ask supervisor)
The resulting lysate was transferred into centrifuge tubes and spun down (4 °C, 18,000 rpm, 10 min, XX34-rotor). The supernatant was discarded, and the pellet was resuspended in 6 M Gua-HCl (pH = 1.5) at 4 °C overnight.

Dialysis of eGFP

Investigator: NA, JH, CR

Aim of the experiment: Purify eGFP

Procedure:

eGFP was thawed on ice
eGFP was then poured into a dialysis hose (cut-off 14 kDa)
The hose was then placed in ice-cold Tris/HCl 20 mM pH 8.0
Dialyzed at 4 °C overnight (XX34 rotor). The supernatant was discarded, and the pellet was

MiniPrep of quickchanged pNGAL146-A2 EspP

Investigator: NA

Aim of the experiment: Extraction of pNGAL146-A2 plasmid from XL1 blue

Procedure:

MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)

Sequencing of P14 (Avi-Tag), P15 (A3C5) & P19 (Quick change (QC) EspP in pNGAL-A2)

Investigator: CR, NA

Aim of the experiment: Sequencing of P14 (Avi-Tag), P15 (A3C5) & P19 (Quick change (QC) EspP in pNGAL-A2)

Procedure:

Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
The different plasmids we prepared received the following barcodes:
P14 : FR11326653
P15 : FR11326655
P19 (K4): FR11326654
P16 (K1): FR11326652
P17 (K2): FR11326651
P18 (K3): FR11326650

Digestion of P16 , P17, P18 & P19 (all QC EspP in pNGAL-A2) with AgeI & HindIII + analytical gel

Investigator: NA, JH, CR

Aim of the experiment: Verification of success of quickchange

Procedure:

analytic digestion with: 0,25 µl HindIII (HF), 0,25 µl AgeI (HF), 1 µl SmartCut Buffer, 500 ng plasmid-DNA, fill up with ddH2O (Vtotal= 10µL)
10 µl on 2% agarose gel for electrophoresis

Results: No signal at 600 bp --> quickchange seems to be successful (waiting for sequencing)

Thursday, May 19th

Re-Sequencing of P19

Investigator: CR

Aim of the experiment: Re-Sequencing of P19

Procedure:Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)

The different plasmids we prepared received the following barcodes:

P19 (K4): FR11326649

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CG

Aim of the experiment: Re-Trafo of pSB1C3 RFP for later on: digestion, dephosphorylation and cloning

Procedure: transformation according to protocol of P4 E. Coli XL1

Result: plates (LB Cam) in incubator for further processing (37 °C)

Streptavidin refolding

Investigator: JB

Aim of the experiment: Refolding of denaturated Streptavidin

Procedure: After the pellet had almost completely dissolved in 6M GdmCl, the solution was spun down (4°C, 20 mins, 18,000 rpm). The supernatant was transferred carefully into a falcon tube and the pellet was cast away. Via a hydraulic pump (flow rate: 2x10 ml/min) the lysate was transferred Into 5L PBS 1x. Afterwards the pump was cleaned with technical isopropanol and ELGA water. The solution was stirred overnight at 4°C for refolding.

Biotinylation of BSA

Investigator: JB

Aim of the experiment: Biotinylation of BSA

Procedure: A 100 µM (=6.8 mg/ml) solution of BSA (Albumin fraction V, pH=7, in the fridge in the central lab) was created (V=10 ml). 220 µl of a 100 mM Biotin stock were added. The mixture was stored overnight Iin the fridge (4°C).

Result: Hopefully biotinylated BSA mixture in the fridge (4°C).

Friday, May 20th

Qualitative analysis of streptavidin expression

Investigator: CG

Aim of the experiment: SDS gel analysis of recombinant strepatividin expression

Procedure: mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining

Result:

1. Lane: 8 µl Marker (Thermo Fisher #26610)
2. Lane: 12 µl culture aliquot, before induction
3. Lane: 12 µl culture aliquot, after induction
4. Lane: 3 µl culture aliquot of the lysed pelet, Strepatvidin expected at about 16 kDa
5. Lane: 3 µl culture aliquot of the supernatend after lysis, no Strepatvidin expected at about 16 kDa
6. Lane: 1.5 µl culture aliquot of the lysed pelet, Strepatvidin expected at about 16 kDa
7. Lane: 1.5 µl culture aliquot of the supernatend after lysis, no Streptavidin expected at about 16 kDa

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: LK

Aim of the experiment: Inoculation of pre-culture with E. coli XL1 (pSb1C3 -RFP) in LB-Chloramphenicol-medium

Procedure: Picking of colonies for E. coli XL1 (pSb1C3 -RFP) Inoculate in 5 ml LB-Chloramphenicol-medium Incubate at 37°C over night at 200 rpm

Transformation of Biobricks in XL1-blue

Investigator: NA, JH

Aim of the experiment: Transformation

Procedure: -10 µl dd H2O in well of interest (standard distribution kit) -1 µl Plasmid (out of well) to cells -Transformation according to the SOP Used bricks: K577893, B0015, R0040, B0032, I14033, K747096

Ammonium sulfate precipitation of streptavidin

Investigator: JB

Aim of the experiment: Reduction of the protein solution volume and precipitation of streptavidin

Procedure: The 5 L protein solution was spun down (20 mins, 5,000 rpm) and the supernatant transferred into a beaker. In order to lower the volume of the solution for ammonium sulfate precipitation, the solution was first filtered via a membrane crossflow pump (membrane: Sartocon 0.45 µm, thick membrane).

Dialysis of biotinylated BSA

Investigator: NA

Aim of the experiment: purification of biotinylated BSA

Procedure: dialysis against Tris/HCl 20 mM, pH 8, 10 mM NaCl over night; cut off : 14 kDa

Week 2 (May 23rd - May 29th)

Monday, May 23th

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CR

Aim of the experiment: Cloning of A3C5 and Avi-Tag into pSB1C3

Procedure:

MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
pSB1C3 was digested with AgeI and NgOMIV (10 µL plasmid + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 14 µL ddH2O; incubation for 1h, 37°C)
FastAP was added and the reaction was incubated for another 2h at 37°C
The digestion was purified by gelelctrophoresis (1%, 75V, 1h)
Plasmid backbone was cut from the gel

Results:

Signal 1: linearized pSB1C3 (successfull digestion)

Signal 2: supercoiled pSB1C3 (digestion not successfull)

Signal 3: RFP-generator

--> next time gel should run longer (just if you need the back bone)

Filtration of Streptavidin and precipitation with Ammonium-sulfate

Investigator: MP, CR

Aim of the experiment: Concentration of Streptavidin

Procedure: The solution was filtered via a membrane crossflow pump (membrane: Sartocon 0.45 µm, thick membrane). The final volum was 0.5L The solution was precipitated by addition of Ammonium-sulfate (2 steps: 1. 40% Ammonium-sulfate; 2. 70% Ammonium-sulfate) After the first addition of ammonium-sulfate the solution was stirred (1h, 4°C) Afterwards the solution was centrifuged (10.000 rpm; 30 min) and the supernatant was used for the second precipitation step The solution was stirred again (over night, 4°C)

Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam

Investigator: JH, JL

Aim of the experiment:

Procedure: Add 50 µL chloramphenicol in 50 mL LB-medium Picking colonies from K577893; B0015; B0032 (in pSB1C3) * Inoculate 4 mL medium (CAM) Incubate at 37°C over night

Following cultures didn´t grow and were therefore not inoculated:

R0040; K747096; I14033

Retransformation of Biobricks in XL1-blue

Investigator: JH, JL, EF

Aim of the experiment: Transformation

Procedure: 10 µl dd H2O in well of interest (standard distribution kit) 1 µl Plasmid (out of well) to cells Transformation according to the SOP Used bricks: K577893, B0015, R0040, B0032, I14033, K747096

Tuesday, May 24th

Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam

Investigator: CR

Aim of the experiment:

Procedure: Add 50 µL chloramphenicol in 50 mL LB-medium Picking colonies from K577893; B0015; B0032 (in pSB1C3) * Inoculate 4 mL medium (CAM) Incubate at 37°C over night

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CR

Aim of the experiment: Gelextraction of Signal 1 from pSB1C3-digestion

Procedure: Gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen)

Ammonium sulfate precipitation

Investigator: JB

Aim of the experiment: Precipitation the 70% saturated ammonium sulfate solution

Procedure: The ammonium sulfate solution, which actually was a suspension, was transferred into centrifuge tubes and spun down (10,000 rpm, 45 mins). As it turns out, unfortunately too much ammonium sulfate was used for the precipitation (wrong table). The precipitate was brought back into solution (20 mM Tris/HCl, pH 8.0) and loaded onto an SDS gel for analysis, along with other samples (flowthrough of the filtration from the day before).

MiniPrep of BioBricks in pSB1C3 (inoculated on May 23th)

Investigator: JH

Aim of the experiment: Extraction of BioBricks B0032, B0015 and K577893 in pSB1C3 from XL1 blue

Procedure: MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen) concentrations measured (in ng/µL): (B0032) 360.2; (B0015) 254.9; (K577893) 99.2

Sequencing of P23 (weak RBS), P24 (double terminator) & P24 (Tet repressed GFP)

Investigator: JH

Aim of the experiment: Sequencing of P23, P24 & P25 (x2)

Procedure: Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)

The different plasmids we prepared received the following barcodes:

P23 (VF2) : FR11326647
P24 (VF2) : FR11326646
P25 (VF2) : FR11326645
P25 (VR) : FR11326644

Wednesday, May 25th

Inoculation of pre-culture with tet-repressed GFP (P25) in LB-Cam

Investigator: NA

Procedure: Add 50 µL chloramphenicol to 50 mL LB-medium Picking colonies from plate (BL21) Incubate over night at 37°C => dismissed, because plasmid sequence was inaccurate

MiniPrep of K747096, I14033, R0040, B0015, K577893 and B0032

Investigator: CR

Aim of the experiment: MiniPrep of BioBricks

Procedure: MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen) Concentrations were measured (in ng/µL):

K747096: 286.2
I14033: 246.1
R0040: 243.5
B0015: 244.1
K577893: 440.9
B0032: 259.7

PCR of P19 (QC EspP) with O3 and O4

Investigator: CR

Aim of the experiment: Amplification of quickchanged EspP

Procedure:

reaction was performed after manufacturer's protocol (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
274,4 pg Plasmid were used for amplification (1 µL)
PCR program (standard):

Step	Temperature [°C]	Time [s]
initial Denaturation	98	30
35 cycles	98	10
	72	30
	72	60
final Extension	72	5
Hold	4	ꝏ

PCR product was purified accoding to manufacturer's protocol (PCR puification kit, Qiagen)
DNA was eluted 40 µL EB buffer

Digestion of PCR of EspP (P19 with O3 and O4)

Investigator: CR

Aim of the experiment: Digestion of EspP with AgeI and NgoMIV to ligate it in pSB1C3 later on

Procedure:

Batch for preparative digestion:

Volume	Reagent
38.5 µL	PCR product P19 with O3 and O4
1 µL	AgeI
1 µL	NgoMIV
5 µL	CutSmart buffer
4.5 µL	ddH₂O
50 µL	TOTAL

Incubation for 2 h at 37 °C

Sequencing of P26 (CMV promotor), P27 (p cat promotor), P28 (Tet repressible promotor), P30 (Tet repressed GFP)

Investigator: NA

Aim of the experiment: Sequencing of P26, P27, P28 & P30 (x2)

Procedure: Sequencing batches were prepared after manufacturer's protocol (15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer) The different plasmids we prepared received the following barcodes: P26 (VF2) : FR11326643 P27 (VF2) : FR11326642 P28 (VF2) : FR11326641 P30 (VF2) : FR11326640 P30 (VR): FR11326639

Ion exchange chromatography of eGFP

Investigator: NA, JB,JL

Aim of the experiment: purification of eGFP

Procedure:

use Äkta-Purifier (Q-column for eGFP (quarternary ammonium as stationary phase)). Ask Andy before use!
Pump A: running buffer (20 mM Tris/HCl pH 8); pump B: elution buffer (20 mM Tris/HCl pH 8 and 1,000 mM (1 M) NaCl
basic pumpwash before start
injection in loop
gradient of ion strength on column.

Results: Elution of eGFP at ~200 mM NaCl.

Thursday, May 26th

Inoculation of cultures with XL-1 F11 and F12 clones

Investigator: JB

Aim of the experiment: Inoculation of a 5 ml culture with a clone of the previously transformed F11 (Avi-Tag) F12 (Antibody-binding site).

Cloning of ligation F14 +F13

Investigator: MP, EF, JH

Aim of the experiment: new biobrick EspP in pSB1C3

Procedure: F14 was purified by gelelctrophoresis (1%, 90 V, 40 min) gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen) ligation of F14 (EspP) with F13 (dephos. PSB1C3) transformation according to protocol in competent E.coli XL1 blue

Results:

Transformation of Biobrick B0034 in XL1-blue

Investigator: JH

Aim of the experiment: Transformation

Procedure:

10 µl ddH2O in well of interest (standard distribution kit, plate 4, well 1N)
1 µl Plasmid (out of well) to cells
Transformation according to the SOP (incl. rescue)

Transformation of Biobricks K577895 and K577894 in XL1-blue

Investigator: NA

Aim of the experiment: Transformation

Procedure:

10 µl ddH2O in well of interest (standard distribution kit, plate 1, wells 14B / 12P)
1 µl Plasmid (out of well) to cells
Transformation according to the SOP (incl. rescue)

SDS-PAGE of eGFP-fractions after IEC

Investigator: NA, CG

Procedure: mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining Concentrations were measured via nanodrop (A280, extinction coefficient: 55000 M−1cm−1)

Result: concentrations in mg/ml 1. Lane: 8 µl Marker 2. Lane: 10 µl of fraction 10; c= 0 3. Lane: 10 µl of fraction 11; c= 0,15 4. Lane: 10 µl of fraction 12; c= 0,77 5. Lane: 10 µl of fraction 13; c= 0,29 6. Lane: 10 µl of fraction 14; c= 0,4 7. Lane: 10 µl of fraction 15; c= 0,144 8. Lane: 10 µl of fraction 16; c= 0,085

$Muc16 SDS-PAGE of eGFP-fractions after IEC.png$

eGFP is clearly detectable at about 27 kDa. The most pure fractions 12 and 13 were pooled for later biotinylation.

Friday, May 27th

Inoculation of pre-cultures with B0034 (strong RBS), K577894 (Tet repressed YFP), KK577895 (Tet repressed RFP), F13+F14

Investigator: JH

Procedure:

Add 50 µL ampicillin(B0034)/chloramphenicol(K5777894, K577895, F13+F14) to 50 mL LB-medium
Picking colonies from plate (XL1 blue; all rescue)
Incubate over night at 37°C

Inoculation of BL21 (pASK75 (SA1)) culture in 2 L TB-Medium and induction of streptavidin production by addition of tetracycline

Investigator: NA

Aim of the experiment: Production of streptavidin

Procedure:

Ampicillin (2 mL) was added to the Medium (1:1000)
The pre-culture (50 mL) was poured into the Medium
Culture was incubated at 37°C and 140 rpm until OD550 reached 0.5
To induce streptavidin expression anhydro-tetrazycline (200 µL) was added to the culture (1:10000)
The culture was incubated at 37°C and 140 rpm for 4 hours

Result: Streptavidin expression by BL21

Re-sequencing of P30 (Tet repressed GFP in pSB1C3)

Investigator: NA

Aim of the experiment: Purification and sequencing of P30

Procedure:

P30 was heated up to 100 °C and centrifugated afterwards to remove proteins from Promotor (if there are some), the supernatant is sequenced
Sequencing batches were prepared after manufacturer's protocol

(15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer)
The different plasmids we prepared received the following barcodes:
- P30 (VF2) : FR11326638

Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium

Investigator: JH, NA

Aim of the experiment: Recombinant expression and purification of Streptavidin

Procedure:

After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4°C, 5000 rpm, 20 mins, F 4X1L rotor)
The supernatant was cast away and the pellet was stored at –20 °C

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CG

Aim of the experiment: MiniPrep of cloned pSB1C3-A3C5 and –AviTag Plasmids

Procedure:

MiniPrep of inoculated precultures was performed according to manufacturer’s protocol (QIAprep MiniPrep, Qiagen)
Concentrations were measured (in ng/µL):

Colony 1 of pSB1C3- AviTag P32: 120 Colony 2 of pSB1C3- AviTag P33: 110 Colony 1 of pSB1C3-A3C5 P34: 126 Colony 2 of pSB1C3-A3C5 P35: 188

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: NA, JH, CG

Aim of the experiment: Initial vector digestion was performed with NgoMiV and AgeI, producing complementary overhangs. Religated pSB1C3 (due to incomplete vector dephosphorylation) loses the AgeI recognition sequence. Therefore plasmids without insert should run in the supercoiled position at about 1.5 kb, plasmids with inserts should run in the linearised position at 3 kb. Single enzyme digestion was chosen, because the insert is too small to be solved on a gel.

Procedure:

analytic digestion: 3 µl of plasmid DNA P32 to P35 (about 300 ng) were digested with 0.3 µl AgeI-HF in 1 µl CutSmart Buffer and 5.7 µl H2O. The reaction was incubated for 2 h at 37°C.
5 µl digestion mix were loaded on a 1% agarose gel for electrophoresis, 1 kb ladder

Result:

P32 to P35 might carry the insert because they all appear in the linearized position at 3 kb
Therefore plasmid sequencing should confirm the result.

Lane 1: 1 kb ladder Lane 3: P32 Lane 4: P33 Lane 5: P34 Lane 6: P35

Week 3 (May 30th - June 5th)

Monday, May 30th

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CR

Aim of the experiment: Sequencing of P32 and P35

Procedure:

Sequencing batches were prepared according to manufacturers protocol (Mix2Seq Kit, Eurofins Genomics): 15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer (10 µM)

The plasmids received the following barcodes:
- P32 (VF2) : FR11326637
- P35 (VF2) : FR11326636

Religation of F13 (digest of pSB1C3 with AgeI and NgoMIV) and transformation in XL1 blue

Investigator: CR

Aim of the experiment: Re-ligate digested and dephosphorylated pSB1C3 and transformation in XL1blue

Procedure:

Plasmid was ligated with the T4 DNA Ligase following the manufacturer’s protocol (NEB)
52 ng Vector DNA were used
The Ligation mix was incubated for 30 min at RT
7 μL Ligation mixed were used for the transformation of 50 μL XL1 blue.
Transformation was performed following the SOP

Result:

5 clones on plate

Inoculation of pre-cultures with B0034 (strong RBS), K577894 (TET repressed YFP), KK577895 (Tet repressed RFP), F13+F14

Investigator: CR

Procedure:

Add 50 µL ampicillin(B0034)/chloramphenicol(K5777894, K577895, F13+F14) to 50 mL LB-medium
Picking colonies from plate (XL1 blue; all rescue)
Incubate over night at 37°C

Tuesday, May 31th

Dialysis of eGFP

Investigator: NA

Aim of the experiment: Changing the buffer of eGFP for biotinylation (from TRIS to PBS)

Procedure:

eGFP was poured in a dialysis hose (cut-off 14 kDa)
The hose was then placed in ice cold PBS pH 7.4
The dialysis took place at 4°C overnight

Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium

Investigator: JB, NA

Aim of the experiment: Recombinant expression and purification of Streptavidin

Procedure:

The pellet was transferred into a beaker of sufficient size and resuspended in fridge-cooled Tris Buffer B (50 mM Tris/HCl (pH = 8.0), 1 mM EDTA)
The solution was homogenized in the PANDA (see SOP)
The resulting lysate was transferred into centrifuge tubes and spun down (4°C, 18,000 rpm, 30 mins, SS34-rotor). The supernatant was cast away and the pellet was resuspended in 6M Gua-HCl (pH = 1.5) at 4°C overnight.

Transformation of P30 (Tet repressed GFP)

Investigator: NA

Aim of the experiment: expression of tet-repressed GFP in E. Coli BL21

Procedure: transformation in competent E. Coli BL21 according to protocol

Result: plates (LB Cam) in incubator for further processing (37 °C)

Cloning of A3C5 and Avi-Tag into pSB1C3

Investigator: CR, JH

Aim of the experiment: Preculture of pSB1C3 (F13+F14) was red See if RFP-generator is still inside the pSB1C3 See if ligation of EspP was successful

Procedure:

MiniPrep of P39 was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
pSB1C3 was digested with AgeI and NgOMIV (1.5 µL P39 + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 22.5 µL ddH2O; incubation for 2h, 37°C)
FastAP was added and the reaction was incubated for another 10min at 37°C
FastAP was inactivated by heating the mix to 75°C for 10min.
The digestion was purified by gelelctrophoresis (1%, 75V, 1h)

Results:

Unknown signals. Repeat transformation, digestion, dephosphorylation and ligation of pSB1C3

Re-transformation of P4 (pSB1C3 (RFP-generator)) in XL1 blue

Investigator: JH, CR

Aim of the experiment: Transformation

Procedure:

2 μL P4 were used for transformation of XL1 blue
Transformation was performed according to SOP (incl. rescue plate)

Competent E. coli XL1 cells

Investigator: JB

Aim of the experiment: Generation of competent E.coli XL1 cells

Procedure:

5 ml LB w.o. antibiotics (sterile)
Inoculation of one colony of E.coli XL1 cells
Incubate overnight at 37°C

Wednesday, June 1th

eGFP Biotinylation

Investigator: CG

Aim of the experiment: Biotinylation of dialysed eGFP past IEC

Procedure:

The average concentration of the pooled factions 12 and 13 should be about 0.5 mg/ml (=19 µM)
10 ml of a 100 mM Biotin stock-solution was prepared (340 mg)
3.5 ml of eGFP were biotinylated with 12 µl 100 µM Biotin-solution (20x molar excess)
Incubation at 4 °C overnight

pSB1C3 vector backbone preperation

Investigator: CG

Aim of the experiment: Inoculation of two colonies pSB1C3-RFP Generator

Procedure:

2x 5 ml LB+Cam medium (1:1000)
Picking colonies from plate (XL1 blue, rescue)
Incubate overnight at 37°C

Generation of GFP expressing E. coli cells

Investigator: CG

Aim of the experiment: Inoculation of BL21 transformed cell with P30

Procedure:

50 ml LB+Cam medium (1:1000)
Picking colonies from plate (BL21, rescue)
Incubate over night at 37°C

Competent E. coli XL1 cells

Investigator: JB

Aim of the experiment: Generation of competent E. coli XL1 cells

Procedure:

Inoculated 500 µl preculture in 50 ml LB media w.o. antibiotics
Incubated and shaken at 37°C until the OD550 reached 0.44
Transferred into a falcon tube and incubated on ice for 10 mins
Spun down at 3000 g for 10 mins at 4°C, supernatant cast away
Pellet resuspended in 40 ml fridge-cooled MgCl2 (100 mM), once again spun down at 4°C for 10 mins at 3000 g
Supernatant cast away, pellet resuspended in 20 ml cold CaCl2 (50 mM)
Incubation on ice for 30 mins
Centrifugation repeated, supernatant cast away
Pellet resuspended in 2 ml of CaCl2 (50 mM) and glycerol (15%)-solution, aliquoted (50 µl each), frozen in liquid nitrogen and stored at -80°C for further use

Cloning of Pcat-RBS-construct in pSB1A2

Investigator: CG, JH, CR

Aim of the experiment: Pcat (I14033) was cut out of P27 and ligated into P38 for generating the Pcat-RBS (B0034) construct.

Procedure:

P27 was digested with EcoRI and SpeI (4 µL P27 + 1.5 µL EcoRI + 1.5 µL SpeI + 3 µL CutSmart + 20 µL ddH2O; incubation for 2h, 37°C)
P38 was digested with EcoRI and XbaI (10 µL P27 + 1.5 µL EcoRI + 1.5 µL XbaI + 3 µL CutSmart + 14 µL ddH2O; incubation for 2h, 37°C)
Preperative gel electrophoresis was performed
For P27 the signal at about 50 bp was cut out and gel extracted according to manufacturer's protocol (Gelextractionkit, Qiagen): 5.9 ng/µl
For P30 the signal at about 2.1 kb was cut out and gel extracted according to manufacturer's protocol (Gelextractionkit, Qiagen): 8.9 ng/µl
Ligation according to SOP

Purification of streptavidin

Investigator: JB

Aim of the experiment: Refolding denaturized streptavidin

Procedure:

the GdmCl-solved streptavidin was spun down using an SS-34 rotor (~60 min, 18,000 rpm, 4°C)
The supernatant containing the solved and denaturized protein was transferred into a falcon tube, the pellet cast away
The protein solution was slowly dripped into 4 l of cooled 1x PBS (in the 4°C room) using a hydraulic pump and stirred overnight

Tuesday, June 2th

Preparation of pSB1C3 for further use

Investigator: CR

Aim of the experiment: Digestion of pSB1C3 to remove RFP-generator

Procedure:

MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
P40 was digested with AgeI and NgOMIV (2.5 µL P40 + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 21.5 µL ddH2O)
Incubation over night at 37°C

Generation of GFP expressing E. coli cells

Investigator: CG, JH

Aim of the experiment: Various inductor concentrations

Procedure:

12x 5 ml LB+Cam media were inoculated with 50 µl preculture
when cultures reached OD550 of 0.5, they were induced with tetrazycline-anhydride of various concentrations (0 ng/µl, 20 ng/µl, 40 ng/µl etc., 200 ng/µl)
t=0, =30, =90, =150, =210, =270 a 100 µl aliquot of each culture was stored at 4 °C in the refrigerator

Dialysis of biotinylated eGFP

Investigator: JH, JB

Aim of the experiment: Purification of biotinylated eGFP

Procedure:

eGFP was poured in a dialysis hose (cut-off 14 kDa)
The hose was then placed in 2 L ice cold Tris/HCl 20 mM pH 8.0
The dialysis took place at 4°C over night

Ligation of F17.1 (p(cat)) and F18 (stron RBS) and transformation in XL1 blue

Investigator: JH

Aim of the experiment: Ligation and transformation in XL1blue

Procedure:

Plasmid was ligated with the T4 DNA Ligase following the manufacturer’s protocol (NEB)
9 µL F18 (B0034 in pSB1A2; RBS) and 1 µL of F17.1 (I14033; P(cat)) were used [AmpR]
The Ligation mix was incubated for at least 2h at RT
7 μL Ligation mixed were used for the transformation of 50 μL XL1 blue
Transformation was performed following the SOP [AmpR], incl. rescue plate

Friday, June 3th

Cloning of F8 (A3C5), F9 (Avi-Tag) and F14 (EspP) into F20

Investigator: CR

Aim of the experiment: Cloning of A3C5, Avi-Tag and into pSB1C3

Procedure:

FastAP was added and the digestion of F20 and was incubated for another 15 min at 37°C
The digestion was purified by gelelctrophoresis (1%, 75V, 1h)
Plasmid backbone (signal 1) was cut from the gel
Gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen)

Results:

Signal 1: F20

[F20]= 13,8 ng/μL

Generation of GFP expressing E. coli cells

Investigator: CG, NA

Aim of the experiment: SDS PAGE for verification of successful GFP expression

Procedure:

SDS electophoresis according to SOP
Lane 1: #12, 90 min
Lane 2: #12, 150 min
Lane 3: #12, 210 min
Lane 4: #12, 270 min
Lane 5: 8 µl

Results:

Inoculation of colonies from F19 (pcat-strong RBS)

Investigator: CG

Aim of the experiment: three colonies were picked from yesterdays transformation

Procedure:

3x 5 ml LB+Amp media
Each culture was inoculated with one colony
Incubation at 37°C overnight

Cloning of F8 (A3C5), F9 (Avi-Tag) and F14 (EspP) into F20 (pSB1C3)

Investigator: CG

Aim of the experiment: Ligation of F21, F22 and F23 into F20 and transformation

Procedure:

Ligation was performed according to the SOP with: 0.7 µl F8 (1:10) / 9.3 µl F20, 0.7 µl F9 (1:10) / 9.3 µl F20, 9.1 µl F14 / 0.9 µl F20
Transformation was performed according to the SOP on LB Cam-Agar

Precipitation of Streptavidin

Investigator: NA, JB, LK

Aim of the Experiment: Purification of Streptavidin

Procedure:

Slowly add (NH4+)2SO42- until the concentration reaches 40% (23,1 g/100mL) while stirring
Let it stir over night to ensure complete precipitation
Centrifuge at 8500 rpm at 4°C for 15min (rotor: SLA1500), dismiss the pellet and use the supernatant for further processing
Slowly add (NH4+)2SO42- until the concentration reaches 70% (19,1 g/100mL) while stirring
Let it stir over night (slowly to avoid foaming)
Centrifuge at 8500 rpm at 4°C for 15min (rotor: SLA1500), dismiss the supernatant and use the pellet for further processing
Resuspend the protein pellet in a minimum volume of TRIS/HCl; pH 8; 20mM (NO SALT) (6 mL per pellet), the pellets where then united and titrated with Buffer until the solution became clear. Total amount of buffer: 40mL
Transfer to 50 mL Falcon Tubes and centrifuge at full speed for 15 min. Filter the supernatant through 45nm sterile filter and keep the pellet (rescue).

Saturday, June 4th

Inoculation of colonies from F21 (pSB1C3 (A3C5)), F22 (pSB1C3 (Avi-Tag)), F23 (pSB1C3 (EspP))

Investigator: NA

Aim of the experiment: three colonies were picked from each transformation

Procedure:

3x 5 ml LB+Cam media for each fragment
Each culture was inoculated with one colony
Incubation at 37°C overnight

MiniPrep of F19 (pSB1A2 (pcat-strong RBS))

Investigator: NA

Aim of the experiment: Extraction of Ligation: F17+F18 (starke RBS+P(cat))

Procedure: MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen) Concentrations: K1= 66,2 ng/µl; K2= 60,2 ng/µl; K3= 104,4 ng/µl

Week 4 (June 6th - June 12th)

Monday, June 6th

Cloning of TetR from p28 into p31 (pSB1C3(weak RBS))

Investigator: LK, JH, NA

Aim of the experiment: Cloning TetR in front of weak RBS in pSB1C3

Procedure:

Digestion of p28 with EcoR1 and Spe1 (20µl DNA, 2,5 µl each enzyme, 5µl CutSmart buffer, 20µl ddH2O) and p31 (4µl DNA, 1µl EcoRI / XbaI, 2µl, 12µl DNA) -> Incubation at 37°C for 2h.
Electrophoresis: 1% Agar, 15 min , 70 V (oben p31 und p41, unten p28)

Gelextraction concentrations: p28 (F25) = 2,3 ng/µl

p31 (F24) = 7,8 ng/µl

Ligation with 6,3 µl vector (F24) and 1,7 µl Insert (F25) + 1µl Buffer + 1µl Ligase over night, 16°C

SDS-PAGE of Streptavidin

Investigator: NA, JH, LK

Procedure: mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining. Concentration of streptavidin was measured via UV/VIS spectroscopy.

c = 23,5 mg/ml

Result:

1. Lane: 8 µl Marker
2. Lane: 5 µl of Streptavidin_1:10
3. Lane: 5 µl of Streptavidin_1:50
4. Lane: 5 µl of Pellet_1:500
5. Lane: 5 µl of after 40% precipitation_1:10
6. Lane: 5 µl of supernatant after 70% precipitation and centrifugation

Successful Streptavidin production verified.

Sequencing of P41 (pSB1C3 (strongRBS-p(cat)))

Investigator: NA

Aim of the experiment: Sequencing of P41

Procedure: Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (100 ng/ µl) and 2 µL sequencing primer (VF2))

The plasmids prepared received the following barcode:

P41 : FR11326633

Tuesday, June 7th

Transformation of P30 (Tet repressed GFP), P36 (Tet repressed RFP), P37 (Tet repressed YFP)

Investigator: NA

Aim of the experiment: Transformation of RFP, GFP and YFP in BL21

Procedure: transformation in competent E. Coli BL21 according to protocol + rescue

Result: plates (LB Cam) in incubator for further processing (37 °C)

MiniPrep of P42 to P50, analytic digestion, sequencing

Investigator: CG

Aim of the experiment: Verification of successful cloning

Procedure: MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)

Concentrations (ng/µl each) for P42: 260, P43: 247, P44: 181, P45: 118, P46: 261, P47: 135, P48: 148, P49: 240, P50: 299
Analytic digestion: 0.3 µl AgeI, 2 µl CutSmart, 6.7 µl H2O for P42, P43, P44, P45, P46, P49, P50 and 0.3 µl EcoRI, 0.3 µl PstI, 2 µl CutSmart, 6.4 µl H2O for 2 h at 37°C
1% agarose gel electrophoresis
Sequencing: P42= FR11326632 (VF2), P45 =FR11326631 (VF2)

Results:

Lane 1: 5 µl 1 kb Ladder
Lane 2-10: Digestion of P42 to P50. P47 and P48 are carrying the insert. All other plasmids are religated and lost their AgeI site, hence they run in the ccc position.

Dialysis of not biotinylated eGFP

Investigator: NA

Aim of the experiment: Purification of eGFP for mass determination

Procedure:

eGFP was poured in a dialysis tubes
The tubes were then placed in ice cold ammonium acetate
The dialysis took place at 4°C over night

Polymerisation attempts

Investigator: JH, CR, CG, JB

Aim of the experiment: Identification of optimal polymerisation conditions for biotinylated eGFP and BSA in a Streptavidin reservoir

Procedure:

variate of compositions for both solutions was examined to modify density properties during “printing”
all compositions can be found in excel sheet

Results:

no or little successful polymerization at Streptavidin concentrations of 4 mg/mL and below; immense density incompatibilities
sucessfull polymerization at Streptavidin concentrations of 10 mg/mL and BSA solution with approx. 15% glycerol
no success with biotinylated eGFP (too few Biotin molecules?!)

Wednesday, June 8th

Sequencing of P36 (Tet repressed RFP) and P37 (Tet repressed YFP)

Investigator: NA

Aim of the experiment: Sequencing of P36 and P37 in both directions

Procedure: Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)

The different plasmids we prepared received the following barcodes:

P36 (VF2): FR11326630
P36 (VR): FR11326629
P37 (VF2): FR11326628
P37 (VR): FR11326627

Dialysis of Streptavidin

Investigator: NA, JH

Aim of the experiment: Purification of Streptavidin (possible ammonium sulfate contamination after precipitation)

Procedure:

Streptavidin was poured in a dialysis hose (cut-off 14 kDa)
The hose was then placed in 3 L ice cold Tris/HCl 20 mM pH 8.0 (no salt)
The dialysis took place at 4°C over night

Polymerisation attempts

Investigator: JH, JB

Aim of the experiment: Identification of optimal polymerisation conditions for biotinylated BSA in a Streptavidin reservoir

Procedure:

variate of compositions for both solutions was examined to modify density properties during “printing” (Streptavidin at 10 mg/mL or higher)
all compositions can be found in excel sheet

Thursday, June 9th

Generation of GFP, YFP, RFP expressing E. coli cells

Investigator: CG

Aim of the experiment: Various inductor concentrations, various fluorescent proteins were expressed in E coli cells

Procedure:

3x 5 ml LB+Cam media were inoculated with 50 µl preculture of GFP (P30), RFP (P36), YFP (P37)
when cultures reached OD550 of 0.5, they were induced with anhydro-tetrazycline of various concentrations (0 ng/µl, 100 ng/ml, 200 ng/ml)
50 ng/ml = 12,5 µl of 1:100 2 mg/ml stock solution, 200 ng/ml = 50 µl of 1:100 2 mg/ml stock solution
t=0, =4 h and stored on ice

Resuts: no fluorescent could be detected. Therefore an overnight induction at 37°C with 1 µM/ml inductor concentration was performed with the RFP plasmid.

Biotinylation of GFP expressing E. coli cells

Investigator: CG

Aim of the experiment: Biotinylation of P30 carrying E. coli cells

Procedure:

850 µl P30 preculture from Thursday 2nd were centrifuged and the supernatend was discarded
Pellet was resuspended in 800 µl PBS-buffer
100 µl 100 mM Biotin-NHS was added
incubation for 4 h at room temperature
Experimenting with some glycerol and streptavidin concentrations. A more structured approach will be done the next day.

Results: A shape thin “sausage” could be detected. Therefore a bigger E. coli culture was biotinylated at 4°C overnight for experimenting with the next day.

Cloning of TetR promotor and weak RBS in pSB1C3

Investigator: CR, JB

Aim of the experiment: MiniPrep and NanoDrop of F26 K1, K2 and K3 Sequencing of P51

Procedure: MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen) Concentrations were as following:

P51: 163,3
P52: 151,7
P53: 140,5

P51 was sequenced:

1. with VF2: FR11326626
2. with VR: FR11326625

Biotinylation of eGFP

Investigator: VL, JB

Aim of the experiment: Biotinylation of eGFP with 200x biotin-NHS molar excess over eGFP (15x excess over surficial K residues). NB: previous trial unsuccessful. Excess of biotin was likely insufficient to ensure efficient biotinylation, esp. since biotin-NHS slowly hydrolyzes in the aqueous environment.

Procedure: 1 ml of eGFP was biotinylated with an 200x excess of biotin in DMF (100 uM; 38 uL), 5.5 h at rt. The solution was dialysed versus 20 mM Tris/HCl pH 8 overnight at 4 °C.

PCR of gene syntheses

Investigator: LK

Aim of the experiment: Amplification od iGEM_1_SA-m1 (F27), iGEM_1_mRuby_EGFR (F28) and iGEM_2_IRES-BirA (F29)

Procedure:

Add 100µl of ddH2O to the gene sythesis samples and incubate for 20 min at 50°C
Dilute samples to a final concentration of max. 1ng/µl (1:10) with water.
Approach:

1µl DNA (diluted)

5µl buffer

0,5µl dNTPs

1,25µl forward Primer VF2

1,25µl reverse Primer VR

0,25µl Q5 Polymerase

Fill up with water up to 25µl

Make sure to pipette everything on ice and add the polymerase at the end
Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)

98°C_1min initiation step

98°C_10sec

66°C_30sec > step 2-4: 35 repeats

72°C_30sec

72°C_2min final step

4°_hold

The samples were then prepared with the PCR Product Purification Kit

Polymerisation experiments for biotinylated eGFP and BSA with Streptavidin

Investigator: JH, CR, JB

Aim of the experiment: Determination of ideal concentrations for both protein interaction partners as well as buffer viscosity (glycerol content etc.) for polymerisation in a test tube

Procedure:

Different concentrations of proteins and glycerol were tested to support stable polymerisation without protein aggregates rising to the surface or sinking to quickly
The experiments done are not going to be further documented as the streptavidin used for the experiments was previously determined in a wrong fashion and was actually considerably lower than expected (4x lower). Streptavidin was, due to that circumstance, concentrated to be able to support experiments with at least 5 mg/ml concentrations
First experiments with concentrated streptavidin seemed promising, though a complete series of experiments with varying parameters should be conducted in the future

Sequencing of P29 (pSB1C3 (double terminator), P36 (pSB1C3 (Tet repressed RFP)) and P37 (pSB1C3 (Tet repressed RFP))

Investigator: JB

Aim of the experiment: Sequencing of P29, P36 and P37

Procedure: According to the manufacturer's protocol.

P29: FR11326624 (VF2)
P36: FR11326623 (VF2)
P37: FR11326621 (VR), FR11326622 (VF2)

Inoculation of (pre)cultures for a pSB1C3 midiprep

Investigator: JB, VM

Aim of the experiment: Massively amplifying the pSB1C3 vector (which will be needed for building up new biobricks) by midiprepping the P40 plasmid (RFP-generator in pSB1C3). Similar to minipreps, but on a greater scale. Procedure: 3 ml precultures were inoculated with a clone from the plate previously used for minipreps. After the precultures had grown for 4 hours (due to shortage of time), 2 x 50 ml cultures were inoculated and shaken overnight at 37°C. The next day, cultures were put into the fridge for storage until Monday.

Week 5 (June 13th - June 19th)

Monday, June 13th

Digestion of gene synthesis iGEM1 and iGEM2

Investigator: LK, JH

Aim of the experiment: Digest F28 (iGEM1) and F29 (iGEM2) in order to ligate them into P40, which was equally digested (to get rid of the rfp-generator and have pSB1C3 as backbone)

Procedure:

30µl of F28 were digested for 3h with SpeI and NgoMIV, and 30 µl of F29 were digested with XbaI and PstI
2 x 20 µl where digested with the equivalent enzymes for 3h
After electrophoresis the bands were cut out and purified

Results: Results show that PCR of F28, F29 might not have worked. P40 was extracted from gel (F30 and F31). PCR of gene synthesis was repeated (50µl!)

Midiprep of P40

Investigator: LK

Aim of the experiment: Purification of P40 from

Procedure:

See protocol of Midiprep kit
1xuse-centrifugation-columns broke in centrifuge during last step, DNA rescue was tried by resuspending rest of the solution in the tube in EB buffer and redo the last steps (isoprop and ethanol precipitation)
Airdry "pellet"(no pellet visible) for 15 min under fume hood and resuspend in 100µl EB Buffer
Measure concentration with nanodrop

Preparation of Collagen + Biotinylation

Investigator: VL, JL

Aim of the experiment: prepare collagen solution + biotinylate small sample

Procedure:

Dissolve 5 g collagen in 50 mL Tris/HCl pH 8 20 mM w/o salt --> 770 uM solution (100 mg/mL)
Sterile filter
Biotinylation: 980 uL Tris buffer + 20 uL collagen solution + 30 uL biotin-NHS (100 mM in DMF, 200x molar excess over collagen monomers)
Reaction time:
Dialyze 4 °C Tris/HCl pH 8 20 mM w/o salt o/n

Transformation of P9 (pASK75)

Investigator: JL, VL

Aim of the experiment: transform streptavidin expression vector P9 (clone 4) into E. coli BL21

Procedure:

Standard (see booklet): 45 s at 42 °C; incubate 1h, 37°C; plate: medium w. chloramphenicol (+ rescue plate) Incubate o/n 37°C.
Wrong antibiotic plate, repeated the next day of the experiment: Massively amplifying the pSB1C3 vector (which will be needed for building up new biobricks) by midiprepping the P40 plasmid (RFP-generator in pSB1C3). Similar to minipreps, but on a greater scale.

Tuesday, June 14th

Mass spectrometry of biotinylated eGFP

Investigator: CR

Aim of the experiment: identify biotinylation degree of eGFP

Procedure:

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Results: about 4-5 biotins per protein. To verify the biotinylation degree the unbiotinylated eGFP will be measured.

Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3

Investigator: CR

Aim of the experiment: Purification of PCR products

Procedure:

Volume of PCR reaction: 50 µL
PCR products were purified by manufacturers protocol (QIAquick PCR purification kit, Qiagen)
Concentration measured by Nanodrop:
F32: 87,5 ng/µL
F33: 68,3 ng/µL
Test if PCR worked:
Samples were applied on a 2% agarose gel and was run at 80 V for 40 min.

Results:

PCR of F28 worked --> F32
PCR of F29 did not work --> wrong primers were used for amplification --> F33 not right (Re-Do PCR with appropriate primers

Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3

Investigator: CG

Aim of the experiment: Digestion of F32 (SpeI, NgoMIV) and F33 (XbaI, PstI)

Procedure:

Digestion F32: 27 µl of F32 (2.4 µg), 5 µl CutSmart Buffer, 1.5 µl SpeI, 2 µl NgoMIV, 14.5 µl H2O
Digestion F33: 27 µl of F32 (1.8 µg), 5 µl CutSmart Buffer, 1.5 µl XbaI, 1.5 µl PstI, 15 µl H2O
Incubation for 3 h at 37°C
Preperative gel:

Gelextraction of F32 upper band and F32 lower band was executed by manufacturers protocol (Qiagen)
F32 upper band (mRuby) was named F34 (=10 g/yl)
F32 lower band (eGFR) was named F35 (=6 ng/yl)

Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3

Investigator: CR

Aim of the experiment: Ligation of F34 (mRuby) and F35 (eGFR) in F30 (pSB1C3); Tranformation in XL1blue

Procedure:

Ligation mixtures were prepared as following:
F34: 8.0 μL F34, 2 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase)
F35: 7.6 μL F35, 2.4 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase)
Ligation was incubated for 30 min at RT

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Re-Sequencing of P37 (Tet repressed YFP)

Investigator: CG

Aim of the experiment:

Purification and sequencing of P30

Procedure:

P30 was heated up to 100 °C and centrifugated afterwards to remove proteins from Promotor (if there are some), the supernatant is sequenced
Sequencing batches were prepared after manufacturer's protocol
(15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer)
The plasmid we prepared received the following barcode: P37 (VF2) : FR11326620

Streptavidin expression

Investigator: CR

Aim of the experiment: Transformation of P9 (pASK74 (SA1)) in BL21

Procedure:

Transformation was executed following SOP
Transformed cells were plated on LB medium (Amp) (50 µL and rescue (50 µL)

Dialysis of Streptavidin and biotinylated BSA

Investigator: CR

Aim of the experiment: Streptavidin and bitinylated BSA are both in Tris/HCl without salt. SInce we will perform later experiments in salty solutions the dialysis was performed against 137 mM NaCl (Saltconcetration of PBS)

Procedure:

3 L Tris/HCl NaCl solution was prepared
Dialysis was prepared according to SOP
Cut off Dialysis hose: 14 kDa

Inoculation of (pre)cultures of P40 for a pSB1C3 midiprep [repeat]

Investigator: JH

Aim of the experiment: Massively amplifying the pSB1C3 vector by midiprepping the P40 plasmid (RFP-generator in pSB1C3)

Procedure: four 4 ml precultures were inoculated with a clone from the plate previously used for minipreps. After the precultures had grown for 6 hours, 50 ml cultures were inoculated and shaken overnight at 37°C.

Subcloning of P41 (strong RBS-p(cat)) Insert into pSB1C3

Investigator: JH

Aim of the experiment: Moving P41 (pSB1A2; Pcat+weakRBS) to pSB1C3 for biobrick submission

Procedure:

Digestion of P41 with XbaI and PstI (10 µl DNA, 1,5 µl each enzyme, 3 µl CutSmart buffer x10, 14 µl ddH2O) -> Incubation at 37°C for 2h.
Electrophoresis: 2% Agar, 40 min , 90 V (1kb ladder, empty, P41, 100b ladder)
GelExtraction

Resuts: no visible signal of insert at approx. 100b. Area was cut blind for GelEx. No DNA in the sample according to NanoDrop measurement. Repeated the next day.

Inoculation of colonies from NanoLuc

Investigator: JH

Procedure:

2x 4 ml LB+Cam media
Each culture was inoculated with one colony
Incubation at 37°C overnight

Wednesday, June 15th

Subcloning of P41 (strong RBS-p(cat)) Insert into pSB1C3

Investigator: CG

Aim of the experiment: Moving P41 (pSB1A2; Pcat+weakRBS) to pSB1C3 for biobrick submission. No gel extraction was performed because the fragement is too small to visualize on the gel.

Procedure:

Digestion of P41 with XbaI and PstI (10 µl DNA, 1,5 µl each enzyme, 3 µl CutSmart buffer x10, 1 µl FastAP, 13 µl ddH2O) -> Incubation at 37°C for 2 h, heat inactivation at 80°C for 20 min.

fragement is to small to visualize on agel.

Subcloning into F31: 3.8 μL F38, 6.2 μL F31, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase according to the SOP
Transformation into E. coli XL1 according to the SOP

Miniprep of pSB1C3(Nanoluc)

Investigator: LK

Aim of the experiment: Preperation of a BioBrick with NanoLuciferase in pSB1C3

Procedure:

The Miniprep was done according to the protocol.
The two tubes where pooled.
The new Plasmid is found under P54 and was sent to sequencing.

Polymerisation

Investigator: EU

Aim of the experiment: Determine optimal polymerisation conditions for BSA and Collagen

Procedure: The experiment was performed in a 96 Well plate:

Results: maximum concentration of Streptavidin and biotinylated Protein works best. Collagen does not work. Glycerolconcentrations do not inhibit interaction. Reaction might be to slow at given concentrations to be effective in printing process.

MidiPrep of pSB1C3 with RFP generator (P4)

Investigator: NA

Aim of the experiment: purification of pSB1C3 with RFP generator for further processing (P56)

Procedure:

MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)

Results: Concentration very low (12ng/μL), but high volume (500 μL)

Thursday, June 16th

MiniPrep of F36 (Ligation mRuby in pSB1C3) K1 & K2, F37 (Ligation EGFR in pSB1C3), I13453 (pBad promotor) K1 & K2, K577881 (pC+AraC+pBad+GFPc) K1 & K2

Investigator: CR

Aim of the experiment: isolate Plasmids

Procedure:

MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
Plasmids were named as following: [concentration]

F36 K1: P57 [212,9 ng/μL]

F36 K2: P58 [181,3 ng/μL]

F37: P59 [195,5 ng/μL]

K577881 K1: P60 [557,2 ng/μL]

K577881 K2: P61 [791,9 ng/μL]

I13453 K1: P62 [130 ng/μL]

I13453 K2: P63 [460 ng/μL]

Sequencing of P29 (double terminator), P36 (Tet repressed RFP) and P37 (Tet repressed YFP)

Investigator: JB

Aim of the experiment: Sequencing of P56, P57, P59, P61 and P62

Procedure: According to the manufacturer's protocol.

P56: FR11326618 (VF2)
P57: FR11326617 (VF2)
P59: FR11326616 (VF2)
P61: FR11326613 (VR), FR11326615 (VF2)
P63: FR11326614 (VF2)

MidiPrep P4 (pSB1C3)

Investigator: VL

Aim of the experiment: isolate Plasmids

Procedure:

MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen). Centrifugation steps at 20,000 g performed at 12,500 rpm in special centrifugation tubes. Since only one column was left, both prepped cell pellets were applied to one column. Flow-through and wash was collected.
Conc:

Amplification of BioBricks (overnight cultures for minipreps)

Investigator: JB

Aim of the experiment: Inoculation of 5 ml overnight cultures for minipreps. The following biobricks were used:

BBa_K157012
BBa_K243004
BBa_K243006
BBa_K157001
BBa_K243005
BBa_I712009
BBa_K404108
BBa_K782061
BBa_K1371012
BBa_K782060

Procedure:

Three hours of incubation of the tubes containing the bacterial agar at 37°C (Note: 12 hours are actually recommende)
Inoculation of two times 5 ml preculture containing the appropriate antibiotic per clone. For KanRAmpR (reistance against both ampicillin and kanamycin) it was only selected for ampicillin.
Incubation shaking overnight at 37°C

PCR Amplification of genesynthesis 2 (F29; IRES-BirA)

Investigator: LK

Aim of the experiment: Amplification of Genesynthesis_2 (IHRES_BirA_StrepTag)

Procedure: A 50µl approach was made:

33,5 µl Water
2µl DNA (F29, diluted 1:10)
2,5µl of each Primer (O11 and O12 c:10µM)
0,5µl dNTPmix
5µl Reaction buffer
0,5µl Q5-Polymerase
The Annealing Temp. was set an 58°C
Next step is to run an analytic gel (band should be visible at 1,5 kB)

Friday, June 17th

Cloning of genesynthesis 2 (IRES-BirA) into pSB1C3

Investigator: CG, NA, JH

Aim of the experiment: Purification oft he PCR reaction, gel verification, restriction digestion (F29), ligation with F31 and transformation

Procedure:

Yesterdays PCR was purified according to Qiagen PCR purification kit
An anlaytic gel electrophoresis was performed on a 1% gel with 4 µl purified PCR product
Restriction digest: 26 µl purified PCR product, 1.5 µl XbaI, 1.5 µl PstI, 5 µl NEB SmartCut, 16 µl H2O. Incubation for 2 h at 37°C.
Gel extraction
Ligation: F31
Transformation

Results: Gel electrophoresis after PCR purification exhibit a thin signal at 1.5 kb. Next time 1:30 min for elongation time might increase the signal.

Miniprep new iGEM BioBricks

Investigator: VL

Aim of the experiment: Purify plasmid DNA from transformed cells

Procedure:

Miniprep according to manual (pellet centrifuged 5000 rpm, 10 min, 4 °C)
Elution with 50 uL EB Buffer
Concentrations (all ng/uL):

K782061 (a) 172.9, (b) 53.0

K243006 (a) 241.1, (b) 58.6

K1371012 (a) 138.0, (b) 43.0

K157001 (a) 184.3, (b) 186.4

K782060 (a) 339.0, (b) 254.0

K243005 (a) 62.3, (b) 176.2

K243004 (a) 122.3, (b) 110.3

I711009 (a) 185.2, (b) 174.7

K157012 (a) 181.2, (b) 195.3

K404108 (a) 116.4, (b) 142.5

MidiPrep of pSB1C3 with RFP generator (P4)

Investigator: NA

Aim of the experiment: purification of pSB1C3 with RFP-Reportercasette for further processing (P74)

Procedure: MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)

Results:

Cloning of IRES-BirA (F33->F40) into digested F31 (pSB1C3)

Investigator: JH, LK

Aim of the experiment: Ligation of IRES-BirA (F29->F33->F40) into F31 (digested P40 by XbaI and PstI = pSB1C3 without insert), gelelectrophoresis and tranformation in XL1blue

Procedure:

F33 (PCR product of F29/gen synthesis 2) was digested with XbaI and PstI
Gelextraction of band at 1500 bp was executed by manufacturers protocol (Qiagen)
intermediate result: F40 with 6.6 ng/µL
Ligation mixtures were prepared as following:
9.6 µL F40, 0.4 µL F31, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
Transformation: (Saturday)
Transformation of Ligation (F29+F31) into XL-1 blue was done according to the SOP. The plate was incubated until Sunday at 37°C.
3mL-cultures in LB+ 30µg/ml cam where inoculated on Sunday
Mini-prep according to manufacturer's protocol was done on Monday.

PCR, purification and digestion of P19 (EspP) and F28 (mRuby EGFR) for BioBrick creation

Investigator: JB, LK

Aim of the experiment: Amplification of EspP from P19 and mRuby/EGFR (F28) for creation of Biobricks

Procedure (for both fragments):

PCR according to the SOP (primers for P19: O13 and O03, primers for F28: VR and VF2)
PCR purification via the purification kit according to the manufacturer's protocol (concentrations: P19(EspP):119,5 ng/µl F28(mRuby):56,2ng/µl
Analysis on an 1% agarose gel using 5 µl purified PCR product
Restriction digestion with NgoMIV/SpeI (for both cases)
40µl DNA
1,5µl of each Enzyme
2µl ddH2O
5µl CutSmart Buffer
The tubes where incubated at 37°C for ~2 days.

Results: Analytical gel electrophoresis after PCR purification shows thick bands at roughly 1000 bp

Still to do:

Gel extraction of both signals for F28 and one signal for EspP-PCR
Ligation with appropriate vector (e.g. F30)
Transformation

Minipreps of F39 (strong RBS-pcat in pSB1C3)

Investigator: JB

Aim of the experiment: Amplification of F39 (ligation, pCat with strong RBS)

Procedure:

Miniprep according to the manufacturer's protocol
Resulting plasmid: P76
Concentration: 52 ng/µl

Minipreps of pSB1C3 with RFP generator (P4)

Investigator: JH

Aim of the experiment: purification of pSB1C3 with RFP-Reportercasette for further processing (P75)

Procedure:

Minipreps according to the manufacturer's protocol (with 8* 6 mL culture)
Resulting plasmid: P75
Concentration: 142.2 ng/µl [~200 µL]

Inoculation of colony from NanoLuc [P54, Repeat]

Investigator: JH

Procedure:

5 ml LB+Cam media
culture was inoculated with one colony
Incubation at 37°C overnight

Saturday, June 18th

Miniprep of P54 (NanoLuc)

Investigator: LK

Aim of the experiment: Purification of P54 (NanoLuc)

Procedure:

Miniprep according to the manufacturer's protocol
Resulting plasmid: pSB1C3 mit NanoLuc (P54, von )
Concentration: 497,9 ng/µl

Hybridisation of O19 and O20 (StrepTag)

Investigator: LK

Aim of the experiment: Hybridisation of the Strep-Oligos

Procedure: 2µl of each Oligo where diluted in 16µl ddH2O and incubated for 10 min. at 95°. Cooling down at RT for at least half an hour. Stored in fridge

Week 6 (June 20th - June 26th)

Monday, June 20th

Miniprep of F42 (IRES-BirA in pSB1C3)

Investigator: LK

Aim of the experiment: Purification of IRES-BirA Plasmids

Procedure:

Miniprep according to the manufacturer's protocol
Resulting plasmid: pSB1C3 with IRES-BirA

Next Steps:

analytical digestion with EcoRI+PstI and gel (expected bands at 1500 and 2000 Bp)
Sequencing

Results: Concentration: 583,5 ng/µl

PCR and Purification of BirA

Investigator: LK, JB

Aim of the experiment: Amplification of BirA-construct

Procedure:

PCR according to the SOP (primers: O17 and O18)
PCR purification via the purification kit according to the manufacturer's protocol
Analysis on an 1% agarose gel using 5 µl purified PCR product

Results:

Concentration: 185,8 ng/µl --> F41
Analytical gel shows no significant band at 960 Bp -->Repeat

Next Steps:

Repetition of PCR and analytical gel!

Gel and Gelextraction of P19 (QC EspP) and F28 (EspP and mRuby)

Investigator: LK

Aim of the experiment: Purification of both constructs for Ligation

Procedure:

Preperative gel according to SOP
The Purification was done according to the manufacturer's protocol. The EGFR gel-fragment was eluted in 50µl and the mRuby-fragment in 30µl (because of thin band)

Results:

One thick band just before 1000Bp and one lighter band just before 750 Bp. This fits to the lengths of EspP and mRuby.
Concentrations: EspP(now F43): 49,5ng/µl mRuby(now F44): 9,9ng/µl

Next Steps:

Ligation into pSB1C3

Sequencing of F42 (pSB1C3(IRES-BirA)), P54 (pSB1C3(NanoLuc)) , P74 (pSB1C3(RFP generator)) and P76 (pSB1C3(strong RBS-pCat))

Investigator: JL

Aim of the experiment: Sequencing of F42, P54, P74 and P76 in forward direction.

Procedure: Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)

The different plasmids we prepared received the following barcodes:

F42 (VF2): FR11326601
P54 (VF2): FR11326600
P74 (VF2): FR11326599
P76 (VF2): FR11326598

PCR and Purification of genesynthesis 6 (iGEM6) Streptavidin/Traptactin

Investigator: NA

Aim of the experiment: Amplification of gen synthesis 6

Procedure: PCR according to the SOP (primers: VF2 and VR)

Next Steps:

PCR purification via the purification kit according to the manufacturer's protocol
Analysis on an 1% agarose gel using 5 µl purified PCR product
PCR purification via the purification kit according to the manufacturer's protocol
Analysis on an 1% agarose gel using 5 µl purified PCR product

PCR and Purification of BirA (F41)

Investigator: NA

Aim of the experiment: Amplification of BirA (F29)

Procedure: PCR according to the SOP (primers: O17 and O18)

Next Steps:

PCR purification via the purification kit according to the manufacturer's protocol
Analysis on an 1% agarose gel using 5 µl purified PCR product
PCR purification via the purification kit according to the manufacturer's protocol
Analysis on an 1% agarose gel using 5 µl purified PCR product

--> repeat with gene-synthesis 2 (F29 may not be the gene-synthesis 2)

Ligations of StrepTag, EspP and mRuby3 with F30 (digested pSB1C3)

Investigator: JH

Aim of the experiment: Ligations of StrepTag (O19+O20), EspP (F43) and mRuby3 (F44) into F30 (NgoMIV and SpeI; pSB1C3 without insert)

Procedure:

Ligation mixtures were prepared as following:
O19+O20: 1.7 (O19+O20), 8.3 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
F43: 4.6 μL F43, 5.4 µL F30, 2 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
F44: 8.1 μL F44, 1.9 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
Ligation was incubated overnight at 16 °C

Digestion of GSY5 (Streptactin; F27)

Investigator: LK

Aim of the experiment: Restricting GSY5 into StrepActin fragment (Streptavidin mutant) and Leptin fragment (Leptin is for Volker)

Procedure:

Restriction mix:

32µl DNA (F27)

10µl ddH2O

1µl of each enzyme (SpeI, HindIII, SapI)

5µl cut smart buffer

Next Steps:

Preperative gel, 1,5% Agarose, cut out and purify bands at 80 Bp and 425 Bp. (80 is leptin for volker and 425 is StreptActin for further cloning into pASK)

Results:

Tuesday, June 21st

Plating of BioBricks that didn't survive sequencing

Investigator: JB

Aim of the experiment: Instead of directly inoculating cultures with the transformed cells from the bacterial agar that was sent by the HQ, the bacterial agar was now used for overnight plating on agar plates containing the appropriate antibiotic resistance.

Procedure: Two methods were used for each BioBrick: For the first method, an inoculation loop was used for plating directly. For the second methods, the inoculation loop was used to inoculate a 50 µl LB culture that

Sequencing of various plasmids

Investigator: CG

Aim of the experiment: Sequencing of various plasmids with either VF2 or VR

Procedure: Refer to the “Inventarliste” for detailed informations on sequencing codes and primers. Sequencing batches were prepared according to manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)

PCR of gene synthesises (iGEM_1) (mRuby_EGFR)

Investigator: CG

Aim of the experiment: iGEM_1_mRuby_EGFR (F28) for preparing the EGFR signal (at about 100 bp)

Procedure: Approach:

1µl DNA (diluted, 1:10)
25 µl 2x MasterMix
0,5µl dNTPs
2,5 µl forward Primer VF2
2,5µl reverse Primer VR
Fill up with water up to 50 µl

Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)

98°C_1min initiation step
98°C_10sec
66°C_30sec > step 2-4: 35 repeats
72°C_30sec
72°C_2min final step
4°_hold

Transformation of Ligations of F50 (StrepTag), F51 (EspP) and F52 (mRuby3) in pSB1C3

Investigator: JH

Aim of the experiment: Transformation of StrepTag (F50), EspP (F51) and mRuby3 (F52) in XL1 blue

Procedure: transformation in competent E. Coli XL1 blue according to protocol + rescue (repeat due to incubation with LB+Cam ! )

Result: plates (LB Cam) in incubator for further processing (37 °C)

Digestion of P9 (pASK75), P74 (pSB1C3), P26 (CMV promotor) and F47 (BirA)

Investigator: JB

Aim of the experiment: Digestion of P9 and P74 to gain the vectors pASK75 and pSB1C3, respectively, as well as digestion of F47 (PCR fragment of BirA) and P26 (CMV promoter) for the ultimate creation of biobricks

Procedure: P74 was digested in a total volume of 30 µl, while the others were digested in a total volume of 50 µl. Enzymes used were:

P74: XbaI and PstI
P9: HindIII and XbaI
F47: Xba I and PstI (didn’t work)
P26: SpeI and PstI

The digestions were incubated at 37°C for 40 minutes and were thereafter inactivated at 80°C for 5 mins.

Inoculation of cultures for minipreps for P76 (pCat + strong RBS)

Investigator: JB

Procedure: Inoculation of 2x5 ml cultures with P76 clones. Incubation at 37°C overnight.

Wednesday, June 22nd

Minipreps of P79 (pCat+RBS)

Investigator: JB

Procedure: According to the manufacturer's protocol.

Results: Concentration 212 ng/µl. Sent to sequencing

Transformation of ligation F56 (pASK75(Streptactin)), P60 (pSB1C3 (pC+AraC+pBad+GFPc)) , P70 (pSB1C3 (short linker))

Investigator: CG

Aim of the experiment:' Transformation of pASK75-Streptactin (F56) into E. coli XL1 blue, K577881 (P60) into BL21 and K243004 (P70) in XL1

Procedure: transformation in competent E. Coli XL1 blue according to protocol

Result: plates (LB + appropriate antibiotic) in incubator for further processing (37 °C)

Inoculation of colonies from K157001 (EGFR signal peptide), EspP (F50), mRuby (F51), Strep-Tag (F52)

Investigator: CG

Procedure:

2x 5 ml LB+Cam (Amp for K157001) media
Each culture was inoculated with one colony, for ligations 2 colonies each
Incubation at 37°C overnight

Plateing of K243004 (short linker), K243005 (middle linker) from stab cultures

Investigator: CG

Procedure: For both biobricks: stabing into the agar with the inocluation loop and resuspending in 50 µl LB media. Plating on Amp-agar.

Digestion of P64 (EGFR sgnal peptide) and P71 (CD4 signal peptide) for cloning into F57 (pSB1C3 (CMV promotor))

Investigator: CG

Aim of the experiment: Digestion of P67 and P71 for cloning the resulting fragments into the digested F57 fragement.

Procedure: both plasmids were digested in 50 µl, 3 µg for each plasmid DNA. 1 µl of XbaI and PstI, 5 µl Buffer, 20 µl DNA, 23 µl H2O. The digestions were incubated at 37°C overnight.

Preparative agarose gels for separation of digestion of P64 (EGFR sgnal peptide) and P71 (CD4 signal peptide)

Investigators: NA, JB

Aim of the experiment: Separation of digestion fragments of both digested PCR fragments as well as vectors

Procedure:

P74: XbaI and PstI -> Fragment corresponding to the pSB1C3 vector isolated
P9: HindIII and XbaI -> Fragment corresponding to the pASK75 vector isolated
F47: Xba I and PstI (didn’t work) –> only one fragment at 3 kbp present (weird since that was a gene synthesis pcr)
P26: SpeI and PstI -> Fragment corresponding to the cmv-promoter isolated

Gelextraction of P9, P74 and P26 was executed by manufacturers protocol (Qiagen)

Results:

F55: pASK75 (2,9 ng/µl)
F56: pSB1C3 (23,6 ng/µl)
F57: CMV-Promotor (5,9 ng/µl)

PCR of GSY2 (IRES-BirA) with O17/18

Investigators: LK

Aim of the experiment: Amplification of BirA, using new dilution of GSY2 this time, because last 2 PCRs showed confusing results (bands at 2500)

Procedure:

PCR was performed according SOP
Primers: O17 and O18
Annealing at 68°C

Next Steps:

PCR-Purification
Analytical Gel
Ligation into pSB1C3

QuickChange-PCR of pASK75 with O21 and O22

Investigators: LK

Aim of the experiment: Deleting NdeI from pASK (P03)

Procedure:

QC-PCR was performed according to SOP
Primers: O-021 and O-022
Annealing at 68°C
Elongation time: 3:30 min

Next Steps:

Digestion with DpnI at 37°C for 1h
Purification?
Preperative Gel (band at 960), purification
Ligation into pSB1C3

Verification of PCR and Digestion of F28 (gene synthesis 1)

Investigator: NA, LK

Aim of the experiment: Verification of successful PCR via gel electrophoresis and preparation of EGFR

Procedure:

Gel electrophoresis with 1 kb-ladder
Digestion: 42µl of PCR Purification, 1,5 µl of each enzyme (NgoMIV and SpeI), 5µl of cut smart buffer.
Incubation at 37°C over night

Results:

Next steps:

Preparative gel and gel extraction
Ligation into pSB1C3

Thursday, June 23th

Miniprep of E. coli Xl1-Blue transformed with ligation product P80/81 (mRuby3 K1/2), P82/83 (EspP K1/2), P84/85 (StrepTag K1/2) and Trafo of K157001

Investigator: Jan, Julian

Aim of the experiment: Miniprep of E. coli Xl1-Blue transformed with ligation product F50(K1,2), F51(K1,2), F52(K1,2) and Trafo of K157001

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
Concentrations:

Plasmid	c [ng/µl]
P80	432,7
P81	294,8
P82	450,5
P83	479,0
P84	108,0
P85	356,0
P86	47,2

PCR of gene synthesises

Investigator: CR

Aim of the experiment: iGEM_1_mRuby_EGFR (F28) for preparing the EGFR signal (at about 100 bp)

Procedure: Approach:

1µl DNA (diluted, 1:10)
25 µl 2x MasterMix
0,5µl dNTPs
2,5 µl forward Primer VF2
2,5µl reverse Primer VR
Fill up with water up to 50 µl

Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)

98°C_1min initiation step
98°C_10sec
66°C_30sec > step 2-4: 35 repeats
72°C_30sec
72°C_2min final step
4°_hold

QuickChange-PCR of pASK with O21 and O22

Investigators: CR

Aim of the experiment: Digestion of PCR product with DpnI to digest methylated DNA

Procedure:

PCR purification of BirA and mRuby/EGFR

Investigator: CR

Aim of the experiment: purification of PCR

Procedure: PCR purification via the purification kit according to the manufacturer's protocol The samples were renamed:

BirA: F59
mRuby/EGFP: F60

The samples were analysed on a 1% agarose gel. Samples were prepared after SOP.

Results:

Transformation of P60 (K577881; pC+AraC+pBad+GFPc K1) and QC P3 (pASK75(SA1))

Investigator: EF, JB

Aim of the experiment: Transformation of Q CP3 in XL1 blue; transformation of p60 in BL21

Procedure: transformation in competent E. Coli BL21 and XL1blue according to protocol

1µl p60 in BL21 7 µl Q CP3 in XL1 blue

Result: plates (+ rescue plates) incubating

Cloning of CD4- and EGFR-signal peptide into pSB1C3-CMV

Investigator: CR

Aim of the experiment: Digestion of P71 and P69 Procedure:

Digestions were prepared as following:
20 µl CD4 (P71); 1 µl XbaI; 1 µl PstI; 5 µl CutSmart; 23 µl ddH2O
7 µl pSB1C3-CMV; P26; 1 µl PstI; 1 µl SpeI; 2 µl CutSmart; µl ddH2O
20 µl EGFR-signal peptide (P67);1 µl XbaI; 1 µl PstI; 5 µl CutSmart; 23 µl ddH2O
Digestions were incubated for 3 h at 37 °C
The Samples CD4- and EGFR-signal peptide were applied to a 2% and the pSB1C3-CMV to a 1% agarose Gel

Results:

--> passt

Next steps:

Ligation of

Cloning of EGFR (F62) / CD4 (F61) signale peptide into pSB1C3-CMV (F63)

Investigator: CG

Aim of the experiment: Gelextraction and ligation of EGFR- and CD4-signal peptide into pSB1C3 and transformation

Procedure:

Gel extraction according to manufacturers protocol (Qiagen): F61 (CD4) 2 ng/µl, F62 (EGFR) 0.6 ng/ µl, F63 (CMV): 45 ng/ µl
Ligation: 1 µl T4 Ligase, 2 µl Ligase buffer, 7 µl H20, 1.8 µl vector and 8.2 µl EGFR insert or 4.3 µl vector and 5.7 µl CD4 insert
Transformation according to SOP
Plating on LB-Cam agar

Friday, June 24th

Analytical digestion and gelelectrophoresis of P83 (EspP K2) and P83 (StrepTag K2)

Investigator: Julian, Niklas, Luisa

Aim of the experiment: Analytical digestion and gelelectrophoresis of P82/83 (EspP K1/2) and P84/85 (StrepTag K1/2).

Procedure:

Batch for analytical digestion for P82-P85 with EcoRI-HF

volume	reagent
0.5/1.0 µl	Plasmid DNA (-/P84)
1 µl	CutSmart buffer (10x)
0.5 µl	EcoRI-HF(10 U/µl)
8/7.5 µl	ddH2O (-/P84)
=10 µl	TOTAL

500px

Sequencing of P80( mRuby3 K1), P83 (EspP K2) and P85 (StrepTag K2)

Investigator: Julian

Aim of the experiment: Sequencing of P80(mRuby3 K1), P83 (EspP K2) and P85 (StrepTag K2)

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer). Sequencing primer VF2 was used

The different vectors we sequenced received the following barcodes:

mRuby3 in pSB1C3 (P80): FR11326590

EspP in pSB1C3 (P83): FR11326588

Streptag in pSB1C3 (P85): FR11326587

Transformation of E. coli XL1 blue with F64 (quickchanged P3(pSAm1))

Investigator: Niklas

Aim of the experiment: Transformation of E. coli XL1 blue.

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

1 µl of DNA was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37 °C.

Gelextraction of F67(BirA), F68(mRuby), F69(EGFR-TMD), F70(pSB1C3) and F71(pSB1C3)

Investigator: Niklas

Aim of the experiment: Gelextraction of F67(BirA(Digest. F59 [EcoRI; SpeI])), F68(mRuby(Digest. F60 [NgoMIV; SpeI])), F69(EGFR-TMD(Digest. F60 [NgoMIV; SpeI]), F70(pSB1C3(digest. P74 [NgoMIV; SpeI]) and F71(pSB1C3(digest. P74 [EcoRI; SpeI])

Procedure:

Gelextraction was performed by manufacturers protocol (Qiagen).

Cloning of F59 (BirA) and F60 (EGFR-TMD) into pSB1C3

Investigator: CR

Aim of the experiment: Generate biobricks with EGFR-TMD and BirA

Procedure:

Digestions were prepared as following:
1. xµl F59 (BirA); 1 µl EcoRI; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
2. 2 µl P74 (pSB1C3 (RFP-generator); 1 µl NgoMIV; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
3. xµl F60 (mRuby/EGFR); 1 µl NgoMIV; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
4. 2 µl P74 (pSB1C3 (RFP-generator), 1 µl EcoRI; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
Digestion was incubated for 3 h at 37 °C

To Do:

Gel (already prepared)
Gelextraction
Ligation
Trafo

Results:

1. band: P74(NgoMiV, SpeI) 2. band: P74 (EcoRI, SpeI)

1. band: F59 2. band: F60

Transformation of EGFR-TMD-pSB1C3 and BirA-pSB1C3 ligations

Investigator: JB

Procedure: According to protocol. Plates were incubated overnight at 37°C.

Chemical biotinylation of BSA

Investigator: MT, JB

Procedure: BSA was chemically biotinylated with a 20x, 40x and 60x molar excess in two different buffers:100 mM Bicin (pH 8.85) and 100 mM borate (pH 8.85) with 50 mM NaCl respectively.

-> A total of six different tubes.

After one hour incubation at RT, the samples were put in the freezer

Inoculation of liquid cultures (F65 and F66)

Investigator: JB

Procedure:

Clones were picked for inoculation of 5 ml liquid cultures containing the appropriate antibiotic
Incubation overnight at 37°C/shaking

Saturday, June 25th

Miniprep of E. coli Xl1-Blue transformed with P60 (mRuby/EGFR),F58 (Ligation pASK75 + Streptactin), F65 (CMV + CD4), F66 (CMV + EGFR), P70 (Short Linker)

Investigator: Niklas

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
Concentrations:

Plasmid	c [ng/µl]
P87	81
P88	34,5
P89	86,3
P90	108,5
P91	417,4

Analytical digestion and gelelectrophoresis of F64 (quickchanged P3, pASK75(SA1)) for verification of success of quickchange

Investigator: Niklas

Procedure:

Analytical digestion with NdeI and gelelectrophoresis. If quickchange worked there should be a band at about 3200 bp (only one restriction site left)

Incubation over night at room temperature.

Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

Just a band showing a few bp (Primer), there is no plasmid band -> Quickchange did not work

Inoculation of colonies from Ligation of F69 + F70 (EGFR-TMD in pSB1C3) and F44 + F33 (mRuby in pSB1C3)

Investigator: Niklas

Procedure:

6x 4 ml LB+Cam media

Each culture was inoculated with one colony

Incubation at 37°C overnight

Sunday, June 26th

Miniprep of E. coli Xl1-Blue transformed with ligation product F44 + F30 (mRuby3 in pSB1C3), F66 + F70 (CMV+EGFR in pSB1C3)

Investigator: Luisa

Aim of the experiment: Extracting F44 + F30 (mRuby3 in pSB1C3), F66 + F70 (CMV+EGFR in pSB1C3) from E.coli XL-1-blue

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
Concentrations:

Plasmid	c [ng/µl]
P92	162,9
P93	447,9

Repetition of Quick-Change PCR of P3 (pASK + SAm1)

Investigator: Luisa

Procedure:

The QC-PCR was performed according the SOP.

Reaction Mix:

volume	reagent
1,25 µl	Primer O21
1,25 µl	Primer O22
1 µl	dNTP-mix
5 µl	Pfu-Ultra-II reaction buffer
1 µl	template DNA (1:10 dilution of p3)
0,5 µl	Pfu-Ultra-II Polymerase
40,5 µl	ddH2O

digestion of PCR-Product with DpnI for 1h at 37°C

now labeled P94

Transformation of E. coli XL1 blue with P94 (quickchanged P3(pSAm1))

Investigator: Luisa

Aim of the experiment: Transformation of E. coli XL1 blue.

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

10 µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspension was plated on ampicillin plates (inclusive rescue plate) for pASK (F72) and on chloramphenicol plates for P92 and P93 and incubated over night at 37 °C in the incubator.

Analytical digestion and gelelectrophoresis of P92 (mRuby), P93 (CMV + EGFR) and P94 (pASK75)

Investigator: Luisa

Aim of the experiment: Analytical digestion and gelelectrophoresis of P92 (mRuby), P93 (CMV + EGFR) and P94 (pASK75).

Procedure:

Batch for analytical digestion for P92 and P93 with EcoRI-HF and PstI-HF

volume	reagent
1 µl	Plasmid DNA
1 µl	CutSmart buffer (10x)
0.5 µl	EcoRI-HF(10 U/µl) and PstI-HF (10 U/µl) for P92/93, NdeI (10 U/µl) for P94
7.5/7 µl	ddH2O
=10 µl	TOTAL

Results:

1. band (P92): no mRuby at 700bp visible, only empty vector
2. band (P93): empty vector and EGFR --> perfect
3. band (P94): no signal at all --> repetition of QC-PCR

Week 7 (June 27th - July 3rd)

Monday, June 27th

Sequencing of P67 (EGFR-Signalpeptid)

Investigator: Niklas

Procedure:

Sequencing batch was prepared after manufacturer's protocol. (15 µl of plasmid DNA (100 ng) and 2 µl sequencing primer (VF2))

FR11326586

Repetition of Quick-Change PCR of P3 (pASK + SAm1)

Investigator: Luisa

Procedure:

The QC-PCR was performed according the SOP.

Reaction Mix:

volume	reagent
1,25 µl	Primer O21
1,25 µl	Primer O22
1 µl	dNTP-mix
5 µl	Pfu-Ultra-II reaction buffer
1 µl	template DNA (1:10 dilution of p3)
0,5 µl	Pfu-Ultra-II Polymerase
40,5 µl	ddH2O

Digestion of PCR-Product with DpnI for 1h at 37°C.

Transformation of 10µl into component E.coli XL-1-blue, according to SOP (1h incubation at 37°C necessary despite AmpR).

PCR of Genesynthesis 3 and 4

Investigator: Luisa

Aim of Experiment: Amplification of Genesynthesis 3 (contains BAP and IGKappa) and 4 (contains A3C5-tag and BM40)

Procedure:

The PCR was performed according the SOP.

Reaction Mix:

volume	reagent
2,5 µl	Primer VF2
2,5 µl	Primer VR2
1 µl	dNTP-mix
10 µl	Q5 Polymerase reaction buffer
1 µl	template DNA (1:10 dilution of p3)
0,5 µl	Q5-Polymerase
18 µl	ddH2O

Setup: iGEM_standard (Promega-cycler)

temperature	time
98°C	2min
98°C	10sec
66°C	30sec
72°C	30sec
72°C	2min
4°C	hold

the batches were then purified using the Quiagen PCR-Purification Kit.

Analytical digestion and gelelectrophoresis of P88 (pASK75(Steptactin)), P89 (pSB1C3(CMV+CD4) and P90 (pSB1C3(CMV+EGFR-Signal peptide)

Investigator: Niklas

Aim of experiment: Analytical digestion and gelelectrophoresis of P88 (pASK75 + Streptactin, former F58), P89 (CMV + CD4, former F65) and P90 (CMV + EGFR-signal-peptide, former F66)

Procedure:

Batches for analytical digestions:

P88: EcoRI

P89: EcoRI and PstI

P90: EcoRI

volume	reagent
5,8/2,3/1,8 µl	Plasmid DNA (P88/P89/P90)
1 µl	CutSmart buffer (10x)
0.5 µl	EcoRI-HF(10 U/µl)/ PstI
required amount for total volume of 10 µl	ddH2O

Ligation of F67 (BirA) and F71 (vector fragment pSB1C3), Transformation of E. coli XL1 blue afterwards

Investigator: Niklas

Aim of the experiment: Ligation of F67 (BirA) and F71 (empty pSB1C3), Transformation of E. coli XL1 blue afterwards.

Procedure:

volume	reagent
2,4 µl	Vektor
7,6 µl	Insert
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	ddH₂O
=20 µl	TOTAL

CaCl2 competent E. coli XL1-Blue cells were taken out of stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 750 µl LB-medium to each tube.

Incubation for 1 hour at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C in the cell-culture shaker.

next step: analytic digestion of transformation was successful

Digestion of PCR on genesynthesis 3 and 4, and pSB1C3

Investigator: Luisa

Aim of experiment: Division of Leptin, IGKappa, A3C5, BM40 and BAP using SapI, HindIII, XbaI, AgeI for both batches.

Procedure:

Batches for analytical digestions:

volume	reagent
1 µl each	enzyme (SapI, HindIII, XbaI, AgeI)
5 µl	CutSmart buffer (10x)
41 µl	DNA (purified PCR-products of GSY3 and 4)

Additionally 10µg of the vector P74 was digested with XbaI and AgeI in 100µl batch (2µl of each enzyme, 10µl of Cut-Smart buffer). Digestion was performed over night and purified via gelelectrophoresis and gelextraction according to the manufacturer's protocoll. --> Now labeled F80.

Preparative digestion and gelelectrophoresis of P80 , P78 and P85

Investigator: Julian

Aim of experiment: Preparative digestion and gelelectrophoresis of P80 (mRuby3), P78 (NanoLuc) and P85 (Strep-Tag)

Procedure:

Batches for analytical digestions:

P80 and P78: EcoRI and AgeI

P85: EcoRI and NgoMIV

volume	reagent
10 µl	Plasmid DNA
32 µl	ddH2O
5 µl	CutSmart buffer (10x)
1.5 µl	each enzyme(10 U/µl)/ PstI
50 µl	TOTAL

Ligation of F75 (mRuby) and F76 (NanoLuc) into F74 (pSB1C3 with Strep-Tag) and Transformation into E. coli XL1 blue

Investigator: Luisa

Aim of the experiment: Ligation of F75 (mRuby) and F76 (NanoLuc) into F74 (pSB1C3+Strep-Tag), Transformation of E. coli XL1 blue afterwards.

Procedure:

volume	reagent
4,3µl(for F75), 8,2µl (for F76)	Vector
12,7µl (F75), 8,8 (F76)	Insert
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
=20 µl	TOTAL

Ligation was incubated at RT for 1,5h.

CaCl2 competent E. coli XL1-Blue cells were taken out of stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 100 µl of competent cells and gently mixed.

15 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

Incubation for 1 hour at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C in the incubator.

Chemical biotinylation of BSA

Investigator: Niklas

Procedure:

BSA was chemically biotinylated with a 20x and 40x molar excess:

10 ml of 100 mM borate buffer with 50 mM NaCl (pH 8.85)

dissolve BSA (10 mg/ml)

Add biotin-NHS-ester: 20,5 mg for 40x molar excess

reaction over night

Tuesday, June 28th

Preparative digestion and gelelectrophoresis of P83 (EspP) and P29 (DoubleTerminator)

Investigator: Julian

Aim of experiment: Preparative digestion and gelelectrophoresis of P83 (EspP) and P29 (DoubleTerminator)

Procedure:

Batches for analytical digestions:

P83: EcoRI and SpeI

P29: EcoRI and XbaI

volume	reagent
6.5/13 µl	Plasmid DNA (P83/P29)
35.5/29 µl	ddH2O (P83/P29)
5 µl	CutSmart buffer (10x)
1.5 µl	each enzyme
50 µl	TOTAL

Preparative gelelectrophoresis was performed at 80 V for 80 min

Gelelectrophoresis of F73 (pSB1C3 digst. EcoRI, AgeI)

Investigator: Julian

Aim of experiment: gelelectrophoresis of P80 (mRuby3), P78 (NanoLuc) and P85 (Strep-Tag)

Procedure: Preparative gelelectrophoresis was performed at 100 V for 45 min using a pocket spanning over the full width of the 1% agarose gel

Wednesday, June 29th

Transformation of F83 (EspP-Fragment in Double Terminator + pSB1C3), F84 (GSY3 + pSB1C3) F85 (GSY4 + pSB1C3)

Investigator: Niklas

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C.

Thursday, June 30th

Transformation of new E. coli XL1-blue (P75), additional plating of untransformated XL1-blue

Aim of experiment: Quality assurance

Investigator: Niklas

Procedure:

the new competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

1 µl of DNA was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C.

additional plating of untransformated XL1-blue on Tet-, Cam-, Amp- and Kan-plates

Result:

After 12 hous of incubation there were some (~20) colonies on the 50µl-plate transformed with Cam-resistence-plasmids. The transformation has been succesful, though cells grow slow.
There were no colonies on the kan-, amp- and cam- plates with the untransformed E.Coli. Hence we can assume that there are no other plasmids with resistences against kan, amp or cam in our batch of competent cells.

There are cells on the tet-plate. This was expected.

Friday, June 31th

Transformation of P9 (pASK with Streptavidin WT) and QC-PCR product into new E. coli XL1-blue

Aim of experiment: Tranforming pASK without NdeI-cutting point into E.coli (two batches from diffrent approches were tested). And Transforming pASK_SA1 into E.coli XL-1-blue.

Investigator: Luisa

Procedure:

the new competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

10 µl of DNA was added to 50 µl of competent cells and gently mixed.

15 min incubation on ice

30 sec. heat shock at 42 °C

Adding of 950 µl LB-medium to each tube. 1h hour incubation at 37°C.

The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30 °C.

Week 8 (July 04–10)

Monday, July 04

Repetition of the Transformation of QC-PCR product into new E. coli XL1-blue

Aim of experiment: Tranforming pASK without NdeI-cutting point into E.coli (two batches from diffrent approches were tested).

Investigator: Luisa

Procedure:

the new competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

10 µl of DNA was added to 50 µl of competent cells and gently mixed.

15 min incubation on ice

30 sec. heat shock at 42 °C

Adding of 950 µl LB-medium to each tube. 1h hour incubation at 37°C.

The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30 °C.

Transformation of P9 (Streptavidin in pASK75) into E. coli BL-21

Aim of experiment: Tranforming pASK with Streptavidin into E.coli BL-21 for Expression.

Investigator: Niklas

Procedure:

the new competent E. coli BL-21 cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

1 µl of DNA was added to 50 µl of competent cells and gently mixed.

15 min incubation on ice

5&nbspmin. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30 °C

Transformation of F94 (hGH polyadenylation sequence and Nanoluc with StrepTag)

Investigator: Javier

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

45 sec. heat shock at 42 °C

Adding of 950 µl LB-medium.

The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C.

Miniprep of E. coli Xl1-Blue transformed with ligation product P108 and P113 (EspP-Fragment in Double Terminator, F81+F82), P109 and P110 (GSY3+ F73 vector AgeI+XbaI ), P111 and P112 (GSY4+ F73 vector AgeI+XbaI)

Investigator: Javier

Aim of the experiment: Extracting P108 and P113 (EspP-Fragment in Double Terminator, F81+F82), P109 and P110 (GSY3+ F73 vector AgeI+XbaI ), P111 and P112 (GSY4+ F73 vector AgeI+XbaI) from E.coli XL-1-blue

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
Concentrations:

Plasmid	c [ng/µl]
P108	116,2
P109	86,6
P110	136,8
P111	144,8
P112	163,2
P113	123,3

Preparative digestion and gelelectrophoresis of P74 (RFP-Gen.)

Investigator: Julian

Aim of experiment: Preparative digestion and gelelectrophoresis of P74 (RFP-Gen.)

Procedure:

Batch for analytical digestion:

P74: EcoRI and SpeI

volume	reagent
2.5 µl	Plasmid DNA
39.5 µl	ddH2O
5 µl	CutSmart buffer (10x)
1.5 µl	each enzyme
50 µl	TOTAL

Preparative gelelectrophoresis was performed at 90 V for 45 min

Result: pSB1C3 (EcoRI und SpeI) F95

File:Muc16 F95 0407.jpeg

Cloning of F96 (BirA in pSB1C3)

Investigator: Julian

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

10 µl of DNA was added to 50 µl of competent cells and gently mixed.

5 min incubation on ice

30 s heat shock at 37 °C

Adding of 950 µl LB-medium

Incubation at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C

Tuesday, July 05th

Preparing of 200 ml TB medium for inoculation of 2 L medium on Thursday

Investigator: Niklas

Procedure:

2.4 g Tryptone 4.8 g yeast extract

800 µl Glycerine

adjust to 180 ml with ELGA-water

seperately: 3.29 g H₂KPO₄ + 0,46 g K₂HPO₄ with ELGA water (Volume = 20 ml)

Digestion of F49 (BirA) with EcoRI and SpeI and cloning in F95 (pSB1C3)

Investigator: Clemens

Procedure:

Digestion of F49 with EcoRI and SpeI

volume	reagent
20 µl	Plasmid DNA (F49)
5 µl	CutSmart buffer (10x)
1 µl	EcoRI-HF(10 U/µl)
1 µl	SpeI(10 U/µl)
23 µl	ddH2O
=50 µl	TOTAL

Digestion was incubated for 1.5 h at 37°C
Digestion was applied to a 1% agarose-gel
Gel ran at 80V for 35 min

File:Muc16 digestF49 0507.jpeg

BirA had a length of 1012 bp
Upper probe was cut from the gel
BirA was purified with gelextraction which was performed by manufacturer's protocol
Concentration was measured
- [F97]= 12.4
Ligation of F97 into pSB1C3 (F95)

volume	reagent
1.2 µl	Vector: pSB1C3 (F95)
8.8 µl	Insert: BirA (F97)
2 µl	T4 DNA Ligase buffer
fill up to 20 µl	dd H₂O
1 µl	T4 ligase
=21 µl	TOTAL

Ligation was incubated at RT for 30 min
Transformation:
- Transformation was performed after SOP
- 7 µl were used for transformation in E. coli XL1blue

Sequencing of P108 - P112

Aim of experiment: Sequencing

Investigator: Niklas

Procedure:

sequencing batches after protocol with following barcodes:

P108 (EspP-Fragment in Double Terminator (F83)) FR11326572 (VF2)

P109 (GSY3+ F73 Leervektor AgeI+XbaI (F84)) FR11326576 (VF2)

P110 (GSY3+ F73 Leervektor AgeI+XbaI (F84)) FR11326575 (VF2)

P111 (GSY4+ F73 Leervektor AgeI+XbaI (F84)) FR11326574 (VF2)

P112 (GSY4+ F73 Leervektor AgeI+XbaI (F84)) FR11326573 (VF2)

NEB Turbo CaCl₂-competent cells

Investigator: Vivien

Procedure:

Inoculate 50 mL LB with 0.5 mL overnight culture of NEB Turbo cells

Incubate at 37 °C for 7 h; final OD₅₀₀: 0.357

Very little growth in the course of the last hour; OD₅₀₀ 0.45 required

Experiment discontinued. Inoculated 3 further colonies in 5 mL LB for o/n growth (37 °C). Repeat experiment on Wed, July 6

Miniprep P114 (NanoLuc + StrepTag + Poly-A in pSB1C3(F94))

Investigator: Niklas

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)

Analytical digestion and gelelectrophoresis of P114 and P115

Investigator: Niklas

Aim of the experiment:

Analytical digestion and gelelectrophoresis of P114 and P115 (NanoLuc + StrepTag + Poly-A in pSB1C3 K1 and K2)

Procedure:

Batch for analytical digestion for P114 and P115 with EcoRI+PstI

volume	reagent
1.75 µl	Plasmid DNA P114/P115
1 µl	cut smart (10x)
0.5 µl	EcoRI
0.5 µl	PstI
6,25 µl	ddH2O
=10 µl	TOTAL

Incubation for 45 min at 37 °C.

Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

File:Muc16 digestP114 P115 0507.jpeg

1 kbp ladder DNA ladder	P114	P115
	X	X

Inoculation of Quick change of P88 (pASK75 (Streptactin)) preculture

Investigator: Clemens

Procedure:

four colonies were picked from plate
Cells were inoculated in 5 mL LB medium (ampicillin 1:1000)

Analytical digestion of P108 and P113 (both EspP + double terminator (F83)) with EoRI and PstI

Investigator: Clemens

Procedure:

Digestion of F49 with EcoRI and SpeI

volume	reagent
1 µl	Plasmid DNA (P108/P113)
1 µl	CutSmart buffer (10x)
0.5 µl	EcoRI-HF(10 U/µl)
0.5 µl	PstI(10 U/µl)
7 µl	ddH2O
=10 µl	TOTAL

Digestion was incubated for 1.5 h at 37°C
Digestion was applied to a 1% agarose-gel
Gel ran at 80V for 35 min

File:Muc16 analyt.digest.P108 P113 0507.jpeg

P108 and P113 showed the right bands

Wednesday, July 06th

Sequencing of P108 (EspP-Fragment in Double Terminator (F83))

Investigator: >Niklas

Procedure:

sequencing batches after protocol with following barcodes:

P108 (EspP-Fragment in Double Terminator (F83)) FR11326572 (VR)

Digestion of P75 (RFP-Generator) with HincII + dephosphorylation

Investigator: Niklas

Aim of experiment: Blunt-Ligation of BirA into pSB1C3

Procedure:

Digestion of P75 (RFP-Generator) with HincII + dephosphorylation

volume	reagent
3 µl	Plasmid DNA (P75)
2 µl	CutSmart buffer (10x)
0.5 µl	HincII
1 µl	Fast AP (for dephosphorylation)
14.5 µl	ddH2O
=20 µl	TOTAL

Digestion was incubated for over night at 37°C

next steps: PCR of GSY2 with O17 and O18 + phosphorylation, Ligation in digested pSB1C3 afterwards

Cloning of A3C5 Tag into the MiddleLinker-Plasmid

Investigator: Christoph

Aim of experiment: Cloning of A3C5 Tag into the MiddleLinker-Plasmid

Procedure:

Digestion of Middle_Linker Plasmid (P69) with AgeI and PstI

volume	reagent
0.3 µl	Plasmid DNA (69)
2 µl	CutSmart buffer (10x)
1 µl	AgeI
1 µl	PstI
1 µl	Fast AP (for dephosphorylation)
14.5 µl	ddH2O
=20 µl	TOTAL

volume	reagent
0.3 µl	Plasmid DNA (P112)
2 µl	CutSmart buffer (10x)
1 µl	NgomIV
1 µl	PstI
14.5 µl	ddH2O
=20 µl	TOTAL

Digestion was incubated for over night at 37°C, heat inactivation at 80°C for 20 min.

volume	reagent
2 µl	digested Middle-Linker (F99)
8 µl	digested A3C5 (F100)
2 µl	10x Ligase Buffer
1 µl	Ligase
7 µl	ddH2O
=20 µl	TOTAL

Transformation according to SOP in E. coli XL1 blue

Picking of of E. coli XL1 blue with Streptactin in quickchanged pASK75, F84 (digested GSY3), F85 (digested GSY4)

Investigator: Niklas

Procedure:

Streptactin in quickchanged pASK75: Colonies were picked from Amp-plates. (10x)

F84/F85: Colonies were picked from Cam-plates. (8x each)

Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contains 4 mL of LB-medium + 4 µL of the proper antibiotic.

These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight

Quick Change of mRuby Plasmids

Investigator: Christoph

Aim of experiment: Correction of wrong amino acid within the mRuby sequence

Procedure:

QC according to manufacturers protocol

volume	reagent
10 ng (= 0,3 µl 1:10)	Plasmid DNA (80)
5 µl	10x Pfu Ultra II Buffer
1.25 µl	O23
1.25 µl	O24
0.5 µl	Pfu Ultra II
1 µl	dNTPs
40.7 µl	ddH2O
=50 µl	TOTAL

volume	reagent
10 ng (= 0,3 µl 1:10)	Plasmid DNA (100)
5 µl	10x Pfu Ultra II Buffer
1.25 µl	O23
1.25 µl	O24
0.5 µl	Pfu Ultra II
1 µl	dNTPs
40.7 µl	ddH2O
=50 µl	TOTAL

PCR: 2 min. 98°C initial denaturation, 10 sec. 98°C, 30 sec. Annealing st 60 °C, 5 min 68°C, 35 Cycles

1 h at 37°C DpnI Digestion

Transformation according to SOP in E. coli XL1 blue, QC on mRuby-Strep (F103) was also transformed in E. coli Turbo cells for further investigating the growth rate

Miniprep of Quick Change of pASK75-Streptactin + analytical digestion with Nde1

Investigator: Jan

Procedure:

Miniprep using the kit according to the manufacturer's protocol.

Although cultures seemed to have grown properly, very low and unreliable DNA concentrations were obtained via Nanodrop measurement and no fragment at all could be detected via analytical agarose gel electrophoresis after 90 minutes digestion with Nde1

Creation of competent NEB Turbo cells

Investigator: Jan

Procedure:

250 µl of precultures were used to inoculate 50 ml LB-medium
After an OD=0.45 was reached, cells were put on ice and made competent according to the manufacturer's protocol
50 µl aliquots of competent cells were frozen in liquid nitrogen and stored at -80°C until further use

Inoculation of a BL21 pBAD-GFP (P60) preculture

Investigator: Jan

Procedure:

A single clone was picked in order to inoculate 5 ml LB medium (+Cam)
Culture was grown overnight at 37°C

Inoculation of a BL21 preculture for Streptavidin production (P8)

Investigator: Jan

Procedure:

A clone was picked for the inoculation of 5 ml LB medium
After 6-8 hours of incubation, the 5 ml preculture was used for the inoculation of a 50 ml LB preculture

Thursday, July 07

PCR Amplification of birA (GSY 2)

Investigator: Vivien

Aim: Amplify birA gene

Procedure:

Prepared PCR mix (25 μL reaction volume): NEB Q5 High-Fidelity 2× Master Mix (12.5 μL), ddH₂O (9.5 μL), F29 (1 μL), O17 and O18 (1 μL each)

Cycling protocol: start 1.5 min, 98 °C; 35 cycles 30 s, 98 °C – 45 s, 72 °C – 30 s, 72 °C; final elongation 5 min, 72 °C; end 4 °C

Purified via Quiagen PCR Purification kit following manufacturer's instructions. DNA eluted from column by adding 50 μL EB buffer and heating at 37 °C for 5 min prior to centrifugation.

Results: DNA concentration: 82.7 ng/μL. Stored as F102 at –20 °C

Induction of Streptavidin

Investigator: Vivien

Aim: Induce streptavidin production

Procedure:

Inoculated 2 L TB medium with 50 mL o/n pre-culture and added 2 mL ampicillin (10 mg/mL in 50% EtOH)
Let grow (37 °C, 200 rpm) until OD₅₀₀=0.622 (c. 2.5 h)
Induced with anhydrotetracycline (1:10,000 i.e. 200 μL of 2 mg/mL stock)
Let grow (37 °C, 200 rpm) for 4 h

Results: Induced culture for harvesting (see below)

Production of eGFP

Investigator: Clemens, Vivien, Christoph

Aim: Produce eGFP

Procedure:

Inoculated 50 mL LB+Cam medium with 0.5 mL o/n pre-culture

Let grow (37 °C, 200 rpm) until OD₅₀₀=0.58

Induced with 0.1 mM arabinose (i.e. 100 μL of 50 mM stock)

After 7 h of induction the cells were stored in the fridge overnight for maturation of the GFP-chromophore

Results:

Harvesting of Streptavidin

Investigator: Niklas

Aim of the experiment: Recombinant expression and purification of streptavidin

Procedure:

After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
The supernatant was discarded, and the pellet was transferred into a Falcon and frozen
next steps: resuspending and homogenizing in the PANDA

Friday, July 08

Analytical Digest of mRuby3 Constructs

Aim of experiment: Verify integration of mRuby3 constructs in F103 and F104

Investigator: Vivien

Procedure:

Mixed 16 μL F103 (or 8 μL F104 plus 8 μL ddH₂O) with 2 μL 10× CutSmart buffer and 1 μL each of EcoRI-HF and PstI-HF (20 μL total volume)

Incubated for 45 min at 37 °C

Subjected to gel electrophoresis (1% agarose, 80 V, 120 min)

Results: No band around 700 bp as expected for mRuby3 constructs

Picking clones and inoculating cultures for F101 and F103

Investigator: Jan

Procedure:

All clones available (only two for F101, one for F103) were picked and used to inoculate 5 ml of LB medium containing the appropriate antibiotic
Cultures were incubated at 37°C overnight

Solubilization, lysis and unfolding of streptavidin

Investigator: Jan

Procedure:

According to protocol -> lysis of pellet (19.2 g) in 58 ml lysis buffer (50 mM Tris/HCl pH 8, 1 mM EDTA)
As only two liters of medium were used, the Panda couldn't be utilized for cell lysis -> French Press was used
Cells were additionally submitted to ultrasonic treatment
Centrifugation of cells, casting away the supernatant and resolubilizing the pellet in 5 ml GdmCl (6M, pH 1.5)

Sequencing of P88

Aim of experiment: Verification of QC

Investigator: Julian

Procedure:

Sequencing batch was prepared after manufacturer's protocol. (15 µl of plasmid DNA (100 ng) and 2 µl sequencing primer (PR1))

FR11326565

Transformation of P75 (RFP-Generator), F101 (middle linker+ A3C5), P125 (dig. GSY4) into E. coli XL1-blue and P75 in NEB Turbo E. coli

Investigator: Niklas, Vivien

Procedure:

the competent E. coli cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

1 µl of DNA (6 µl for Ligation F101) was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

5&nbspmin. heat shock at 37 °C

30 min incubation on ice

Adding of 950 µl LB-medium to each tube.

The cells were plated out on Cam-plates/Amp-plate for F101 (inclusive rescue plate) and incubated over the weekend at 30 °C

QuickChange-PCR of P80 (O23 and O24) and P100 (O19 and O20)

Investigators: Niklas

Aim of the experiment: Changing of amino acid

Procedure:

the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1 µl Polymerase is added)
Annealing at 55°C

volume	reagent
1.25µl	O23/O24 and O19/O20
0,5 µl	dNTP-mix
1 µl	1:100 P80 / P100
2.5 µl	Pfu Ultra II-buffer
0.5 µl	Pfu Ultra II Polymerase
19.25 µl	dd H₂O
4 x 25 µl	TOTAL

Preperative gelelektrophoresis of F102 (PCR of BirA) + phosphorylation and ligation into pSB1C3

Investigator: Luisa

Aim of experiment: Blunt-Ligation of BirA into pSB1C3

Procedure:

The whole PCR-product was applied to a 1% agorose gel. After runnig the gel two lines where visible: one at 1000Bp and one at ~500Bp.

The 1000 Bp band was cut out and purified with the Gelextraction kit according to manufacturer's protocoll. Concentration: 41,5ng/µl.

The DNA was phosphorylated as follows:

volume	reagent
15 µl	DNA (~1pmol)
2 µl	Ligase buffer (10x)
1 µl	T4 Polynukleotide-Kinase (for phosphorylation)
2 µl	ddH2O
=20 µl	TOTAL

The batch was incubated for 20 min at 37°C and then the enzyme was inactivated for 10 min at 75°C.

The phosphorylated DNA was then ligated into prepared (HincII-digested) pSB1C3 as follows:

volume	reagent
2,3 µl	Vector
7,7 µl	Insert (BirA)
2 µl	Ligase Buffer (10x)
1 µl	T4 Ligase
7 µl	ddH2O
=20 µl	TOTAL

next steps: Transformation into E.coli Xl-1-blue.

Digestion of P78, P123 (for BAP-Nanoluc-construct),P122 (IgKappa for CMV-IgKappa-construct), P89, P114 (for CMV-EGFR-Nanoluc-StrepTag-PolyA-construct)

Investigator: Luisa

Aim of experiment: Getting of BAP-Nanoluc-construct, CMV-IgKappa-construct and CMV-EGFR-Nanoluc-StrepTag-PolyA-construct.

Procedure:

DNA was digested according to the following table:

volume	reagent
3 µg (for P78, P123 and P122) and 1,5 µg (for P89, P114)	DNA
5 µl	CutSmart buffer (10x)
1,5 µl of NgoMIV and PstI	for P78
1,5 µl of AgeI and PstI	for P123
1,5 µl of XbaI and PstI	for P122
1,5 µl of AgeI and PstI	for P189
1,5 µl of NgoMIV and PstI	for P123
up to 50µl	ddH2O
=50 µl	TOTAL

Results: Concentrations: P78 now F106: 2,7 ng/µl, P89 now F107: 14,4 ng/µl. Gelextractions of P114, P122 and P123 didn't contain DNA. (To few DNA available)

next steps: Retransformation of verified clones (P114, P89) into Xl-1-blue for amplification of plasmid.

Repetition of digestion of P122 and P123 with more DNA (10µg!), then Gel with 100Bp ladder!

Repetition of digestion of P123 (BAP for BAP-Nanoluc-construct) and P122 (IgKappa for CMV-IgKappa-construct)

Investigator: Luisa

Aim of experiment: Getting of BAP-Nanoluc-construct, CMV-IgKappa-construct

Procedure:

DNA was digested according to the following table:

volume	reagent
10 µg → 20µl	DNA
5 µl	CutSmart buffer (10x)
1,5 µl of AgeI and PstI	for P123
1,5 µl of XbaI and PstI	for P122
up to 50µl	ddH2O
=50 µl	TOTAL

Incubation at 37°C over night.

next steps: Gel with 100Bp ladder and Gelex. Then Ligation with prepared vectors from former digestion (F106 an F63)

Week 9, July 11–17

Monday, July 11

MiniPreps of pSb1C3-Middle Linker+A3C5, -BM40, -CMV-EGFR Retrafo, Streptactin in QC pASK75

Investigator: Christoph

Aim of the experiment: Plasmid preparation, analytic digestion, sequencing

Procedure:

MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)

Analytic digestion with 0.25 µL EcoRI, 0.25 µL PstI (HF) for pSB1C3 plasmids and 0.5 µl NdeI for pASK75-Streptactin, 1 µL SmartCut Buffer, 3 µL plasmid DNA, 5.5 µL H₂O

5 µL on 1% agarose gel electrophoresis

plasmid assignment was tricky because of confusion during the weekend Minipreps

Results:

pASK75-Streptactin clone 1 and 2 were not visible

verified Plasmid names are available after sequencing

Lane 1: 5 µl 1 kb Ladder

Lane 2: 5 µL Plasmid F101 K1 (seems to be pSB1C3-RFP-Generator)

Lane 3: 5 µL Plasmid F101 K2 (seems not to be pSB1C3-RFP-Generator)

Lane 4: 5 µl 100 bp Ladder

Lane 5: 5 µL P125 K1 (seems not to be pSB1C3-RFP-Generator)

Lane 6: 5 µL P125 K2 (seems to be pSB1C3-RFP-Generator)

Preperative digestion of NanoLuc + StrepTag + Poly-A (F112) and cloning behind CMV-EGFR (F107)

Investigator: Christoph, Niklas

Aim of the experiment: preperative digestion for cloning of the construct behind of CMV-EGFR

Procedure:

15 µl P115 (NanoLuc + StrepTag + Poly-A), 1 µl NgoMiV, 1 µl PstI, 3 µl CutSmart buffer, 10 µl H2O

Incubation for 2 h at 37°C

1% gel electrophoresis

Photo

gel extraction according to SOP

Ligation of 2 µl F107 (AgeI, PstI) + 8 µl F112 (NgomIV, PstI) with 2 µl Ligase buffer, 7 µl ddH₂O, 1 µl T4-Ligase for 40 minutes

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

7 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).

Cloning of Nanoluc behind BAP

Investigator: Christoph, Niklas

Aim of the experiment: Cloning of Nanoluc behind BAP based (testing fast cloning strategy)

Procedure:

5 µl P78 (Nanoluc), 0.5 µl NgoMiV, 0.5 µl PstI, 1 µl CutSmart buffer, 2.5 µl H2O, 0.5 SacI = F108
4 µl P123 (pSB1C3-BAP), 0.5 µl AgeI, 0.5 µl PstI, 1 µl CutSmart buffer, 3 µl H2O, 1 µl FastAP = F109

Incubation for 2 h at 37°C, 15 min heat inactivation

Ligation: 2 µl F108 (Nanoluc) + 8 µl F109 (BAP), 2 µl buffer, 1 µl Ligase, 7 µl H2O

Transformation:

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

7 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).

Gel extraction of IgKappa (F111) and cloning behind CMV in pSB1C3 (F63)

Investigator: Christoph, Niklas

Aim of the experiment: gel extraction after digestion for cloning of the construct behind of CMV

Procedure:

1% gel electrophoresis

Photo

gel extraction according to SOP

Ligation of 6.1 µl F111 ( XbaI, PstI) + 3.9 µl F63 (SpeI, PstI) with 2 µl Ligase buffer, 7 µl ddH₂O, 1 µl T4-Ligase for 40 minutes

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

7 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).

Retrafo of P123 (digest. GSY3-BAP)

Investigator: Niklas

Procedure:

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

1 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).

Digestion of quickchanged mRuby (without StrepTag) and transformation of E. coli XL1-Blue afterwards

Investigator: Niklas

Procedure:

the PCR-product is digested by 1 µl DpnI (cuts methylated DNA)

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

7 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).

next steps: 4 Minipreps, test digestion, Sequencing

QuickChange-PCR of P100 (O23 and O23)

Investigators: Julian, Niklas

Aim of the experiment: Changing of amino acid in mRuby3

Procedure:

the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1 µl Polymerase is added)
Annealing at 55°C

volume	reagent
1.25µl	O23/O24
0,5 µl	dNTP-mix
1 µl	1:100 P100
2.5 µl	Pfu Ultra II-buffer
0.5 µl	Pfu Ultra II Polymerase
19.25 µl	dd H₂O
4 x 25 µl	TOTAL

Repeated digestion of P75 (RFP-Generator) with HincII + dephosphorylation

Investigator: Julian

Aim of experiment: Blunt-Ligation of BirA into pSB1C3

Procedure:

Digestion of P75 (RFP-Generator) with HincII + dephosphorylation

volume	reagent
6 µl	Plasmid DNA (P75)
2 µl	CutSmart buffer (10x)
1 µl	HincII
1 µl	Fast AP (for dephosphorylation)
11 µl	ddH2O
=20 µl	TOTAL

Digestion was incubated for 2 hours at 37°C

Ligation of phosphorylated F102 (PCR of BirA) into F113 (RFP-Generator P75 digest. HincII)

Investigator: Julian

Aim of experiment: Blunt-Ligation of BirA into pSB1C3

Procedure:

The phosphorylated DNA (prepared on July 8th) was ligated into F113 (HincII-digested RFP-Generator) as follows:

volume	reagent
4,5 µl	Vector F113
5,7 µl	Insert (BirA)
2 µl	Ligase Buffer (10x)
1 µl	T4 Ligase
7 µl	ddH2O
=20 µl	TOTAL

next steps: Transformation into E.coli NEB Turbo.

Tuesday, July 12

Transformation of BirA–RFP generator ligation (F114) and Re-Transformation of P114

Investigator: Vivien

Aim: Transform NEB Turbo cells

Procedure:

Followed standard transformation protocol (SOP) using 1 μL and 10 μL of P114 and F114, respectively

Incubated at 37 °C for 1:10 h

Plated on LB Cam (50 μL + rescue)

Incubated at 37 °C (start 12:30)

Arabinose Induction Experiment: pBAD–GFP

Investigator: Vivien

Aim: Test different induction concentrations of arabinose

Procedure:

Of 30 °C o/n culture, filled 5 mL each into four 10 mL culture tubes

Induced with 0, 0.1, 1, and 10 mM final conc. of arabinose

Took 0.5 mL sample each and stored at 4 °C

Incubated 5 mL cultures at 30 °C for 4 h

Took another 0.5 mL sample each and stored at 4 °C

Picking Colonies of F101 (P69 Middle Linker – P112 A3C5)

Investigator: Vivien

Aim: Pick transformed colonies

Procedure:

Picked 3 colonies off plate with transformed cells

Let grow at 37 °C in LB Amp (start 11:50 am)

Picking Colonies of F123 (BAP)

Investigator: Vivien

Aim: Pick transformed colonies

Procedure:

Picked 2 colonies off plate with transformed cells

Let grow at 37 °C in LB Cam (start 17:00)

Verification of succesful Quickchange of P141 (pASK75 with Streptactin)

Investigator: Niklas

Procedure:

the Plasmid (5 µl) is digested by 0.5 µl NdeI (Addiition of 1 µl cut smart and 3.5 µl ddH2O)

since the quickchange should eliminate the second Nde-restriction site, there should be one band on the gel

result:

there is no band on the gel (the experiment was repeated multiple times showing the same results)

therefore new primers are designed and ordered

Refolding of Streptavidin

Investigator: Niklas

Procedure:

the sample (pelett dissolved in 6M GdmCl)was spun down (4°C, 20 mins, 18,000 rpm)

the supernatant was transferred carefully into a falcon tube and the pellet was cast away

the supernatant was added dropwise to 1 X PBS (500 ml) and stirred over night

Colony PCR of F110 (BAP+Nanoluc)

Investigator: Vivien, Niklas

Aim: Amplification

Procedure:

samples were prepared with 5 µL Q5-Mastermix, 1 µl VF2-, 1 µL VR-Primer, 2 µL ddH20

four clones were picked and added to the samples respectively

PCR- cycles according to SOP

Lane 1: 1 kb Ladder, Lane 2-5: clones 1-4, 10 µl each

Preparative digestion and gelelectrophoresis of P37 and P26

Investigator: Julian

Aim of experiment: Preparative digestion and gelelectrophoresis of P137 (BM40)and P26 (CMV)

Procedure:

Batches for analytical digestions:

P137: EcoRI and XbaI

P26: EcoRI and SpeI

volume	reagent
23/7 µl	Plasmid DNA P137/P26
19/35 µl	ddH2O P137/P26
5 µl	CutSmart buffer (10x)
1.5 µl	each enzyme(10 U/µl)
50 µl	TOTAL

Preparative gelelectrophoresis was performed at 90 V for 60 min

The whole PCR-product was applied to a 1% agorose gel. After runnig the gel two lines where visible: one at 1000Bp and one at ~500Bp.

The 600/2100 bp band (P26/P137) was cut out and purified with the Gelextraction kit according to manufacturer's protocoll. Concentration: 20.4/33.1 ng/µl. (F115/F116)

File:Muc16 P137-P26 1207.jpeg

Ligation of F115 into F116

Investigator: Julian

Aim of experiment: Ligation of F115 (CMV) into F116 (BM40 in pSB1C3)

Procedure:

volume	reagent
4,3 µl	Vector F116 (BM40 in pSB1C3)
5,7 µl	Insert F115(CMV)
2 µl	Ligase Buffer (10x)
1 µl	T4 Ligase
7 µl	ddH2O
=20 µl	TOTAL

next steps: Transformation into E.coli NEB Turbo.

Transformation of F117 (CMV in pSB1C3 with BM40), F118 (QC P100), F119 (QC P80) and P26 (CMV; Retrafo)

Investigator: Julian

Aim of the experiment: Transformation of CMV in pSB1C3 with BM40 (F117), QC P100 (F118), QC P80 (F119) and P26 in NEB Turbos(F117)/XL1 blue

Procedure: transformation in competent E. coli NEB Turbo (F117)/XL1 blue (rest) according to protocol + rescue

Result: plates (LB Cam) in incubator for further processing (37 °C)

Wednesday, July 13

QuickChange-PCR of P80 (O23 and O24)

Investigators: Christoph

Aim of the experiment: Changing of amino acid in mRuby3

Procedure:

the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1 µl Polymerase is added)
Annealing at 55°C

volume	reagent
1.25µl	O23/O24
0,5 µl	dNTP-mix
1 µl	1:100 P80
2.5 µl	Pfu Ultra II-buffer
0.5 µl	Pfu Ultra II Polymerase
19.25 µl	dd H₂O
4 x 25 µl	TOTAL

Cycling was performed according to SOP.

MiniPrep of Middle Linker-A3C5 construct

Investigator: Christoph

Aim of the experiment: MiniPrep two colonies of Middle Linker-A3C5 construct

Procedure:

MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
Both plasmids were sent to sequencing without analytical digestion because of the short lenght

Cloning of F120 (CMV-IgKappa) and F121 (CMV+EGFR / Nanoluc+StrepTag+PolyA)

Investigator: Christoph

Aim of the experiment: Ligations of F120 (CMV-IgKappa) and F121 (CMV+EGFR / Nanoluc+StrepTag+PolyA) and transformation

Procedure:

Ligation mixtures were prepared as following:
F120: 5 μL F63, 5 µL F111, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
F121: 3 μL F107, 7 μL F112, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
Ligation was incubated for 30 min. at room temperature
transformation was performed according to SOP (with 100 µl cells and 20 µl ligation mix) and plating in LB+Cam agar

Thursday, July 14

MiniPreps of Overnight Cultures

Investigator: Vivien

Aim: Prep plasmid DNA of P26, F110, F117, F114, P114, and P118

Procedure:

MiniPrep performed according to manufacturer's instructions with Qiagen kit

Prior to eluting, 50 μL EB buffer was applied to the membrane, and the columns were heated at 37 °C for 7 min

Results: Plasmid DNA solutions of the following concentrations: P26 (a: 55.1 ng/μL; b: 48.1 ng/μL); F110 (K2: 150.1 ng/μL; K3: 173.0 ng/μL); F117 (a: 257.7 ng/μL; b: 159.0 ng/μL; CMV/BM40: 133.2 ng/μL); F114 (83.1 ng/μL); P114 (a: 26.1 ng/μL; 170.7 ng/μL); P118 (F118?) (a: 248.0 ng/μL; 53.2 ng/μL; 241.3 ng/μL). F110 (K2: FR12904474; K3: FR12904473) and F117 (a: FR12904477; b: FR12904476; CMV/BM40: FR12904475) were sent for sequencing with VF2.

DpnI Digest of mRuby3 QC and Transformation

Investigator: Vivien

Aim: Digest original-sequence plasmid and transform obtained pure quick-changed plasmid

Procedure:

QC was digested with DpnI (40 μL QC, 5 μL 10× CutSmart buffer, 3.5 μL ddH₂O, 1.5 μL DpnI = 50 μL) at 37 °C for 2 h

Digest (10 μL) was directly transformed into Turbo cells following SOP (including 1 h incubation time prior to plating due to chloramphenicol resistance)

Plated 50 μL on LB Cam + rescue plate

Incubated at 37 °C

Result: two plates; remaining digest stored at 4 °C in styrofoam tube rack

Friday, July 15

Inoculation of mRuby Quick change, F120 (CMV+IgKappa) and F121 (CMV+EGFR/Nanoluc+StrepTag+PolyA) preculture and miniprep

Investigator: Niklas, Clemens

Procedure:

6 colonies were picked from plate
Cells were inoculated in 5 mL LB medium (Cam 1:1000)
Fragments were minipreped following manufacturer's protocol (QiaPrep, Qiagen)
Fragments were renamed receiving a P number

Quickchange of P88 (pASK75(Streptactin)) with O-029 and O-030

Investigator: Clemens

Aim: Quickchange pASK75(Streptactin) to erase one NdeI restriction site

Procedure:

For quickchange two seperate batches were prepared:
1. batch: 0.7 µL O-029, 0.5 µL dNTP mix, 2.5 µL buffer, 0.5 µL Pfu ultra polymerase, 1.5 µL P88
2. batch: 0.7 µL O-030, 0.5 µL dNTP mix, 2.5 µL buffer, 0.5 µL Pfu ultra polymerase, 1.5 µL P88
first stage of quickchange PCR was performed as following:

Step	Temperature [°C]	Time [s]
initial Denaturation	98	30
15 cycles	98	10
	55	30
	68	5
final Extension	68	5
Hold	4	ꝏ

PCR batches were mixed and 0.5 µL pfu ultra polymerase was added
Second stage of quickchange PCR was performed as in the following:

Step	Temperature [°C]	Time [s]
initial Denaturation	98	30
35 cycles	98	10
	55	30
	68	5
final Extension	68	5
Hold	4	ꝏ

Cloning of P79 (Nanoluc) into P147 (pSB1C3(BAP))

Investigator: Clemens

Aim:

Procedure:

7 µL P79 were digested with NgOMIV and PstI
10 µL P147 were digested with AgeI and PstI
Digestion products were run on a 1% agarose gel
Both fragments could be cut from the gel
Fragments were purified by gelectraction following manufacturer's protocol (Qiagen)

Fragments were renamed:
- digest P78= F123
- digest P147= F124
9,5 µL F124 and 0.5 µL F123 were ligated following manufacturers protocol (T4 DNA ligase, Thermo scientific)
NEB Turbo were transformed with 7 µL of F125 (ligation F123+F124) following SOP
Cells were plated on CAM LB medium and placed in the incubator at 37°C

Cloning of P145 (Middle Linker +A3C5) and P146 (Middle Linker +A3C5) into F70 (Vector fragment pSB1C3)

Investigator: Niklas, Clemens

Procedure:

Ligation:
- 2,5 µL P145 and 1 µL P146 were pooled and digested with NgOMIV and SpeI for 1h at 37°C.
- Full digestion was ligated into 1 µL F70

CaCl₂-competent E. coli XL1-Blue cells were taken from the stock in –80 °C freezer and gently thawed on ice

7 µl of DNA was added to 100 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Add 1 ml LB medium to each tube

Incubation for 55 min at 37 °C in the 180 rpm cell-culture shaker

60 µl of the cell suspension was plated on one chloramphenicol plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 60 µl of LB-medium and this concentrated cell suspension was plated again on a chlorampenicol plate (=rescue plate).

Test digestion of P164 (BirA blunt end ligation) (after miniprep) and P161, P162, and P163 (all QC mRuby)

Investigator: Niklas, Clemens

Aim: Test digestion to see which plasmids contain the right insert

Procedure:

150 ng of plasmid DNA were digested with EcoRI and PstI following SOP
The whole batch was applied to a 1% gel to check for cut inserts.

Results:

FOTO

Blunt end ligation seems to not have worked (P164)
P161, P162 and P163 all still carry the insert

Sequenced: P161= FR12904472 (NA)

Harvesting of Streptavidin

Investigator: Niklas

Aim of the experiment: Recombinant expression and purification of streptavidin

Procedure:

After precipitation in 70 % ammonium sulfate the soluton was spun down in the centrifuge (4°C, 11000 rpm, 40 mins)
The supernatant was discarded, and the pellet was dissolved in 2.2 M ammonium sulfate (18 mL)
the sample was spun down in the centrifuge (4°C, 15000 rpm, 30 mins)
the pellet was dissolved in 1X PBS(16 mL)
next steps: last centrifugation and dialysis against Tris/Hcl (see plan on board)

Week 10, July 18–24

Monday, July 18

Inoculation of precultures for miniprep of F125 (pSB1C3(BAP-NanoLuc)) and F122 (pSB1C3(Middlelinker-A3C5))

Investigator: Clemens

Aim of the experiment:

Miniprep, analytical digestion, analytical gel, sequencing

Procedure:

Three colonies were picked from each plate (F125, F122)
Inoculation was performed according to SOP
Cells grew for 5h
- Cells onlygrew in cultures with F125 (In cultures with F122 there was no pelet)
Miniprep was performed according to manufactrer's protocol
Samples were renamed:
- F125 K1: P168
- F125 K2: P169
- F125 K3: P170

Analytical digestion:
- Each plasmid was digested with EcoRI and PstI

volume	reagent
6 µl	Plasmid DNA P168/P169/P170
1 µl	Cutsmart (10x)
0.5 µl	EcoRI(10 U/µl)
0.5 µl	PstI (20 U/µl)
1 µl	ddH2O
=10 µl	TOTAL

Results:

Foto:

Lane 1: 1kb ladder
Lane 2: P168
Lane 3: P169
Lane 4: P170 --> right signals (2000 bp, ~600 bp(BAP-NanoLuc)

Send for sequencing:
- P170: FR12904468 (VF2)

Analytical digestion of P149 , P150 (both pSB1C3(CMV-IgKappa)), P151, P152 (both pSB1C3(CMV-EGFR-NanoLuc-StrepTag-polyA)), P153, P154 (both QC pSB1C3(mRuby3))

Investigator: Clemens

Aim of the experiment: Analytical digeston to find out if the cloning was successful

Procedure:

measure concentrations of Plasmids (see inventary list)

Analytical digestion:
- Each plasmid was digested with EcoRI and PstI

volume	reagent
3 µl	Plasmid DNA P149/ P150/ P151/ P152/ P153/ P154
1 µl	Cutsmart (10x)
0.5 µl	EcoRI(10 U/µl)
0.5 µl	PstI (20 U/µl)
5 µl	ddH2O
=10 µl	TOTAL

Results:

Foto:

Lane 1: 1kb ladder
Lane 2: P149 --> right signals (2000bp; 730bp)
Lane 3: P150 --> right signals (2000bp; 730bp)
Lane 4: P151
Lane 5: P152 --> right signals (2000bp; 1626bp)
Lane 6: P153 --> very weak signal
Lane 7: P154 --> right signals (2000bp; 700bp)

Send for sequencing:
- P150: FR12904471 (VF2)
- P152: FR12904470 (VF2)
- P154: FR12904469 (VF2)

Transformation of QC of P88 (pASK75(Streptactin))

Investigator: Clemens

Aim of the experiment:

See if quickchange has worked

Procedure:

NEB Turbo cells were transformed with 10 µl of QC P88 according to SOP
Cells were plated on LB medium (Amp) and incubated at 37°C

Digestion of P165 (pSB1C3(CMV-BM40) and cloning of F112 (Nanoluc-StrepTag-polyA) into P165

Investigator: Clemens

Aim of the experiment:

Create biobrick: CMV-BM40-Nanoluc-StrepTag-polyA

Procedure:

Preparative digestion batch was prepared as in the following:

volume	reagent
15 µl	Plasmid DNA P156
3 µl	Cutsmart (10x)
1 µl	AgeI(10 U/µl)
1 µl	PstI(20 U/µl)
10 µl	ddH2O
=30 µl	TOTAL

Digestion was seperated by gelelectrophoresis

Results:

Foto:

Lane 1: 1kb ladder
Lane 2: F126 (digest P165) --> right length

Procedure:

Fragment was cut from the gel and purified by gelextraction which was performed by manufacturer's protocol (Qiagen)

F126 was ligated with F112

Ligation batch:

volume	reagent
2 µl	Vector DNA F126
18 µl	Insert DNA F112
3 µl	T4 ligation buffer (10x)
6 µl	T4 ligase
µl	ddH2O
=30 µl	TOTAL

Ligation was incubated at 37°C for 30 min
NEB Tubros were transformed with F127 (lig. F112+F126)
Cells were plated on LB medium (Cam)

Tuesday, July 19

Inoculation of Precultures of F127 (pSB1C3(CMV-BM40-Nanoluc-StrepTag-polyA))

Investigator: Clemens

Aim: Prepare cells for miniprep of plasmids

Procedure:

six colonies were picked and inoculated in LB medium (CAM)
Plates were incubated on a shaker at 37°C

Results:

cellgrowth ?

Reamplifiying Streptactin from GSY6

Investigator: Christoph

Aim: Reamplifiying Streptactin from GSY6 for further processing in QC reaction (delete NdeI site from pASK)

Procedure:

PCR reaction was prepared according to SOP
Cycling steps were taken from the QC protocol because no further cycler was free

Results:

will be available after DpnI digestion and transformation

QuickChange-PCR of pASK75 with O29 and O30

Investigator: Christoph

Aim: Deleting NdeI from pASK (P10)

Procedure:

QC-PCR was performed according to SOP
Primers: O-029 and O-030
Annealing at 55°C
Elongation time: 5 min
2-step protocol was applied

Miniprep of E. coli Xl1-Blue P171, P172 and P173 (pSB1C3(CMV-BM40-Nanoluc-StrepTag-polyA))

Investigator: Javier

Aim of the experiment: Extracting P171, P172 and P173 (CMV-BM40-Nanoluc-StrepTag-polyA) from E.coli XL-1-blue

Procedure:

Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
Concentrations:

Plasmid	c [ng/µl]
P171	75,4
P172	108,2
P173	66,4

Transformation of F136 (A3C5+Middle-Linker), F137 (EGFR+mRuby-Strep), F138 (mRuby3-Strep+PolyA) and P161 (QC mRuby-Strep)

Investigator: Javier

Aim of the experiment: Transformation of A3C5+Middle-Linker (F136), EGFR+mRuby-Strep (F137), mRuby3-Strep+PolyA (F138) and QC mRuby-Strep (P161) XL1 blue

Procedure: transformation in competent E. coli XL1 blue according to protocol + rescue

Result: plates (LB Cam) in incubator for further processing (37 °C)

Colony PCR of F127 (CMV-BM40-Nanoluc-StrepTag-polyA)

Investigator: Clemens

Aim: See if cloning was successfull

Procedure:

samples wwere prepared with 5 µL Q5-Mastermix, 1 µl VF2-, 1 µL VR-Primer, 2 µL ddH20

six clones were picked and added to the samples respectively

PCR- cycles according to SOP (Annealing-temp: 66°C; Ampflification time: 1.5min)

Results:

Lane 1: 1 kb Ladder
Lane 2: F127 K1
Lane 3: F127 K2
Lane 4: F127 K3
Lane 5: F127 K4
Lane 6: F127 K5
Lane 7: F127 K6

500px

Preparative digestion of P161 (pSB1C3(mRuby3-StrepTag)), P73 (pSB1C3((PolyA)), P96 ((pSB1C3(EGFR-TMD)), P69 (pSB1C3(Middle-linker)) and P112 (pSB1C3(A3C5))

Investigator: Clemens, Christoph, Javier

Aim: Create biobricks

Procedure:

Preparative digestion of P161 and P73

volume	reagent
15 µl/ 20 µl	Plasmid DNA P161/ P73
3 µl/ 3 µl	Cutsmart (10x)
1 µl/ 1 µl	EcoRI/ EcoRI
1 µl/ 1 µl	SpeI/ XbaI
10 µl/ 5 µl	ddH2O/ ddH2O
=30 µl	TOTAL

Preparative digestion of P96 and P161

volume	reagent
10 µl/ 15 µl	Plasmid DNA P96/ P161
3 µl/ 3 µl	Cutsmart (10x)
1 µl/ 1 µl	PstI/ PstI
1 µl/ 1 µl	AgeI/ NgOMIV
15 µl/ 10 µl	ddH2O/ ddH2O
=30 µl	TOTAL

Preparative digestion of P69 and P112

volume	reagent
20 µl/ 15 µl	Plasmid DNA P69/ P112
3 µl/ 3 µl	Cutsmart (10x)
1 µl/ 1 µl	EcoRI/ EcoRI
1 µl/ 1 µl	AgeI/ NgOMIV
5 µl/ 10 µl	ddH2O/ ddH2O
=30 µl	TOTAL

Digestions were incubated at 37°C for 2h
Samples were applied to a 1% agarose gel (40 min; 90V)
Samples were cut from the gel afterwards:
Renamed:
- digest P69: F128
- digest P112: F129
- digest P161: F130
- digest P96: F131
- digest P161: F132
- digest P73: F133

Results:

Fotos

Procedure:

Gelextraction was performed after manufacturers protocol (Qiagen)
After gelextraction concentrations were measured:

Ligation:

volume	reagent
xx µl	Vektor F129
xx µl	Insert F128
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
x µl	ddH₂O
=20 µl	TOTAL

volume	reagent
xx µl	Vektor F131
7xx µl	Insert F130
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
x µl	ddH₂O
=20 µl	TOTAL

volume	reagent
xx µl	Vektor F133
7xx µl	Insert F132
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
x µl	ddH₂O
=20 µl	TOTAL

Ligation was performed according to SOP
Xl1 blue cells were transformed with the Ligations according to SOP

Wednesday, July 20

Analytical digestion and gelelectrophoresis of P171-P173 & QC of P10

Investigator: JB, MT

Aim of experiment: Check if everything is fine.

Procedure:

Digest P171-P173 with XbaI + SpeI and QC of P10 with NedI and incubate 1 h at 37 °C
Run 1 % agarose-gel at least 40 min at 100 V

Results:

Lane1: 1Kb ladder; Lane2: P171; Lane3: P172; Lane4: P173; Lane5: QC of P10

=> P171 was sent for sequencing: FR12904466 => NdeI test digestion shows two signals although there should have been just one

Preparation of GSY 6; F134; F135 for ligation

Investigator: JB, MT

Aim of experiment: Prepare GSY6 for Ligation.

Procedure:

Digestion of GSY6 with SpeI + HindIII
Preparative 1 % Agarose gel 100 V for at least 40 min.
Gel extraction of GSY6, F134, F135 by Quiagen kit.

Results:

GSY6 -> F139 : 2.5 ng/µL
F134 : 4 ng/µL
F135 : 10.2 ng/µL

Preparative agarose gel GSY6:

Ligation & transformation of F134 + F63; F135 + F139

Investigator: JB, MT

Aim of experiment: Ligation & transformation of F134 + F63; F135 + F139

Procedure:

Ligation following SOP(13.02.2013)

F134 + F63 -> F140
F135 + F139 -> F141

transformation following SOP(13.02.2013)

F140 on CAM
F141 on AMP

Results:

  We will see tomorrow, please update this section.

Thursday, July 21

Miniprep of F136 (K1 & K2) (pSB1C3(Middle linker-A3C5)), F137 (K1 & K2) (pSB1C3(EGFR TMD-mRuby3-StepTag)), F138 (K1 & K2) (pSB1C3(mRuby3-StrepTag-polyA) and retrafo of P161 (pSB1C3(mRuby3-StrepTag))

Investigator: Clemens

Aim of experiment: Get plasmids for analytical digestion and sequencing

Procedure:

Minipreps were performed according to manufacturers protocol (Qiagen, QiaPrep)
Samples were renamed afterwards:
- F136 K1: P174
- F136 K2: P175
- F137 K1: P176
- F137 K2: P177
- F138 K1: P178
- F138 K2: P179
- retrafo of P161: P180

Analytical digestion:

volume	reagent
1 µl	Plasmid DNA
1 µl	Cutsmart (10x)
0.5 µl	EcoRI
0.5 µl	PstI
7 µl	ddH2O
=10 µl	TOTAL

Ligation was renamed: F143
Digestion products were seperated via gelelectrophoresis

Results:

Foto:

All plasmids seemed to carry the appropriate insert

Sequencing:

- P175: FR12904465 (VF2)
- P177: FR12904464 (VF2)
- P178: FR12904463 (VF2)

Preparative digestion of P116 (pSB1C3(IgKappa))

Investigator: Clemens, Christoph

Aim of experiment: cloning of CMV in front of IgKappa signal peptide

Procedure:

preparative digestion batch

volume	reagent
10 µl	Plasmid DNA P116
3 µl	Cutsmart (10x)
1 µl	EcoRI
1 µl	XbaI
15 µl	ddH2O
=30 µl	TOTAL

Digestion was applied to a 1% agarose gel (45 min; 90V)
Sample was cut from the gel and gelextraction was performed according to manufacturers protocol

Ligation of Fx and F115 (digest CMV promotor):

Ligation:

volume	reagent
3.9 µl	Vektor F142
6.1 µl	Insert F115
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
20 µl	ddH₂O
=20 µl	TOTAL

Transformation of XL1blue was performed according to SOP
Cells were plated on LB medium (CAM) and incubated over night at 37°C

Friday, July 22

Analytical digestion of pASK_T7 RBS_LCN2_His

Investigator: Luisa

Aim of the experiment: Analytical digestion to find out whether there is more than one NdeI restriction site.

Procedure:

Analytical digestion:
- The plasmid was digested with NdeI and HindIII

volume	reagent
3 µl	Plasmid DNA
1 µl	Cutsmart (10x)
0.5 µl	NdeI
0.5 µl	HindIII
5 µl	ddH2O
=10 µl	TOTAL

Results:

Two bands were visible what means that there is only one NdeI restriction site.

Inoculation of Precultures of F143 (pSB1C3(CMV+IgKappa))

Investigator: Luisa

Aim: Prepare cells for miniprep of plasmids

Procedure:

two colonies were picked and inoculated in LB medium (CAM)
Plates were incubated on a shaker at 37°C over night.

Harvesting of Streptavidin

Investigator: Niklas

Aim of the experiment: Recombinant expression and purification of streptavidin

Procedure:

the solution was spun down in the centrifuge (4°C, 15000 rpm, 20 mins) to remove last contamination
The pellet was discarded and the supernantant was dialysed against 20 mM Tris/HCl (ph 8) witt 50 mM NaCl
last step to do: steril filtration

the concentration was determined via UV/VIS: the absorption at 280 nm is 0.469 (1:100 dilution), this equals a concentration of 62 mg/mL (about 16 mL) (mass 54 kDa; Absorbtion coefficient 40455 1/M*cm

Sequencing of P174(Middle Linker + A3C5)

Investigator: Niklas

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer)

Cloning of P178 (mRubyStrepPolyA) / P180 (mRubyStrep) behind EGFR-TMD in pSB1C3 (P96)

Investigator: Niklas

Procedure:

Preparative digestion:
The Inserts were digested with PstI and NgoMIV

volume	reagent
7.7 / 8.2 µl (about 3µg)	Plasmid DNA
2 µl	Cutsmart (10x)
1 µl	PstI
1 µl	NgoMIV
8.3 / 7.8 µl	ddH2O
=20 µl	TOTAL

both fragments were ligated with F131 (digest P96 [AgeI; PstI])

CaCl2 competent E. coli XL1-Blue cells were taken out of stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 750 µl LB-medium to each tube.

Incubation for 1 hour at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C in the cell-culture shaker.

Results: Cloning didn't work. No colonies on plate. Repeat.

Cloning of Middle Linker before A3C5 in pSB1C3 (Repeat)

Investigator: Julian, Niklas

Procedure:

Preparative digestion:
- The Middle Linker (P69) was digested with EcoRI and AgeI

volume	reagent
30 µl	Plasmid DNA
5 µl	Cutsmart (10x)
1.5 µl	EcoRI
1.5 µl	AgeI
12 µl	ddH2O
=50 µl	TOTAL

the fragment was ligated with F129(digest P112 [EcoRI; NgOMIV])

CaCl2 competent E. coli XL1-Blue cells were taken out of stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 750 µl LB-medium to each tube.

Incubation for 1 hour at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C in the cell-culture shaker.

Week 11, July 25th - July 31st

Monday, July 25

Inoculation of Precultures of F143 (pSB1C3(CMV+IgKappa)), F141new (pASK(Streptactin)), F151 (pSB1C3(middleLinker+A3C5), pASK75_T7-RBS-LCN2-His, F148 (pSB1C3(mRubyStrepPolyA+ CMV-EGFR Signal-Pept)

Investigator: Luisa

Aim: Prepare cells for miniprep of plasmids

Procedure:

Three colonies of each were picked and inoculated in LB medium (CAM) respectively (AMP) fpr pASK.
Plates were incubated on a shaker at 37°C for 6 hours.

MiniPreps and analytical digestion of F143 cultures

Investigator: Luisa

Aim: Prep plasmid DNA of F143 (pSB1C3(CMV + IgKappa)) and checking wheather ligation was successful.

Procedure:

MiniPrep performed according to manufacturer's instructions with Qiagen kit

Prior to eluting, 30 μL EB buffer was applied to the membrane since the pellet was quite small, and the columns were heated at 37 °C for 7 min

Results:

Concentrations: K1 = 230,4ng/µl, K2 = 162,4 ng/µl

Analytical Digestion:

An 20µl batch was prepared for analytical digestion for each of the two clones:

volume	reagent
10 µl	Plasmid DNA
2 µl	Cutsmart (10x)
1 µl	EcoI
1 µl	PstI
6 µl	ddH2O
=20 µl	TOTAL

Results:

Two bands were visible at 750 Bp which is the size of IgKappa and CMV together. Cloning was successful. Sequence still has to be ckecked though.

Cloning of P178 (mRubyStrepPolyA) / P180 (mRubyStrep) behind EGFR-TMD in pSB1C3 (P96). Repetition.

Investigator: Luisa

Aim: See title.

Procedure:

Digestion of P178 and P180: 7µg of DNA were digested.

volume	reagent
18 µl	Plasmid DNA
5 µl	Cutsmart (10x)
2,5 µl	NgoMIV
2,5 µl	PstI
22 µl	ddH2O
=50 µl	TOTAL

Digestion at 37°C for 2,5h.

Cloning of NanoLuc-Strep-PolyA (F112) behind CMV-IgKappa in pSB1C3 (P181).

Investigator: Luisa

Aim: See title.

Procedure:

Digestion of P181:

volume	reagent
10 µl	Plasmid DNA
5 µl	Cutsmart (10x)
2,5 µl	AgeI (20u/µl)
2,5 µl	PstI (20u/µl)
30 µl	ddH2O
=50 µl	TOTAL

Digestion at 37°C for 2,5h.

Digestion and gel-extraction of P178; P180

Investigator: MT

Aim of experiment: Preparation of P178 and P180 for ligation.

Procedure:

Digest P178; P180 with NgoMIV + PstI incubate 1 h at 37 °C
Run 1 % agarose-gel at least 40 min at 100 V
Gel extraction by Quiagen kit.

Results:

P178 [NgoMIV +PstI digest] -> F152: 17 ng/µL
P180 [NgoMIV +PstI digest] -> F153: 8.1 ng/µL

Ligation & transformation of F131 + F152; F131 + F153

Investigator: MT

Aim of experiment: Ligation & transformation of F131 + F152; F131 + F153

Procedure:

Ligation following SOP(13.02.2013)

F131 + F152 -> F154
F131 + F153 -> F155

Transformation following SOP(13.02.2013)

F154 E. coli. turbo CAM
F155 E. coli. turbo CAM

Results:

  We will see tomorrow, please update this section.

Wednesday, July 27th

Minipreps of EGFR-TMD - mRuby - Strep - PolyA (F131+F152) and EGFR-TMD - mRuby - Strep (F131+F153)

Investigator: JB

Results: Procedure according to protocol (spin kit). Resulting plasmids:

EGFR-TMD - mRuby - Strep - PolyA (F131+F152) -> P196, P197 EGFR-TMD - mRuby - Strep (F131+F153) -> P198, P199

Concentrations: P196: 228 ng/µl P197: 212 ng/µl P198: 197 ng/µl P199: 322 ng/µl

Thursday, July 28th

Inoculation of Precultures of F141new (pASK(Streptactin))

Investigator: Luisa

Aim: Prepare cells for miniprep of plasmids

Procedure:

Three colonies of each were picked and inoculated in LB medium (CAM) respectively (AMP) fpr pASK.
Plates were incubated on a shaker at 37°C for 6 hours.

PCR of GSY6

Investigator: Luisa

Aim: Amplification of Streptavidin mutant and Traptactin for further cloning into pASK.

Procedure:

reaction was performed after SOP (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
2ng Plasmid were used for amplification (1 µL)
Primers: VR and VF2

PCR program (standard):

Step	Temperature [°C]	Time [s]
initial Denaturation	98	30
35 cycles	98	10
	66	30
	72	90
final Extension	72	5
Hold	4	ꝏ

PCR product was purified accoding to manufacturer's protocol (PCR puification kit, Qiagen)
DNA was eluted 40 µL EB buffer

Digestion of pASK

Investigator: Luisa

Aim: Preparing pASK for ligation with Streptavidin mutant and Traptactin.

Procedure:

volume	reagent
20 µl	Plasmid DNA
5 µl	Cutsmart (10x)
1,5 µl	NdeI
1,5 µl	HindIII
22 µl	ddH2O
=50 µl	TOTAL

Cloning of Traptactin and Streptavidin mutant into pASK (P191).

Investigator: Luisa

Aim: Preperation of the plasmids for Streptavidin and Traptactin expression in E.coli.

Procedure:

Cutting out the crucial bands from the gel containing the PCR-product and the digested plasmid (P190) and purifiing them with the Gelextraction Kit according to the protocoll. First Gel failed: Very small band with wrong length...--> Repetition of digestion with P190.

The PCR product of GSY6 was extracted from the gel (Band at ~800 Bp) with the Gelextraction Kit and then digested with NdeI and HindIII to get the fragments Streptavidin m1 and Traptactin. Inactivation was performed at 80°C for 10 min.

Concentrations: 33,9ng/µl (GSY6),

Ligation...

Cloning of NanoLuc-Strep-PolyA (F112) behind CMV-IgKappa in pSB1C3 (P182). Repetition.

Investigator: JB

Aim: See title.

Procedure:

Digestion of P182:

volume	reagent
15 µl	Plasmid DNA
3 µl	Cutsmart (10x)
1,5 µl	AgeI (20u/µl)
1,5 µl	PstI (20u/µl)
9 µl	ddH2O
=30 µl	TOTAL

Digestion at 37°C for 2.5h.
Take care: P182 is not sequenced

Retrafos of P178 (mRuby-Strep-PolyA) and P181 (CMV + IgKappa)

Investigator: JB

Results: Transformation according to protocol, plates were incubated at 37°C overnight.

Dialysis of eGFP

Investigator: Julian

Aim of the experiment: Preparation of eGFP for following biotinylation

Procedure:

eGFP was poured in a dialysis hose (cut-off 14 kDa)
The hose was then placed in 4 L ice cold borate buffer 50 mM pH 8.85 (no salt)
The dialysis took place at 4°C over night

Sequencing of P160 (NanoLuc+StrepTag+Poly-A)

Investigator: Julian

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer)

Friday, July 29th

Minipreps of EGFR-TMD - mRuby - Strep - PolyA (F131+F152) and EGFR-TMD - mRuby - Strep (F131+F153)

Investigator: Julian

Procedure:

Procedure according to protocol (spin kit). Resulting plasmids:

CMV+EGFR-SigPep+mRuby3+StrepT+PolyA (F131+F152) -> P200, P201 pASK_T7 RBS_LCN2_His (Vorlage für gewünschte Inserts) -> P202, P203

Results:

Concentrations: P196: 385.3 ng/µl P197: 462.6 ng/µl P198: 84.8 ng/µl P199: 96.0 ng/µl

Send for sequencing:
- P201: FR12904454 (VF2)

Analytical digestion of P202 and P203 (pASK_T7 RBS_LCN2_His)

Investigator: Julian

Aim of the experiment: Controll whether there is more than one NdeI restriction site.

Procedure:

Analytical digestion:
- The plasmid was digested with NdeI and HindIII

volume	reagent
2 µl	Plasmid DNA
1 µl	CutSmart buffer
0.5 µl	NdeI
0.5 µl	HindIII
6 µl	ddH2O
=10 µl	TOTAL

Results:

Two bands were visible what means that there is only one NdeI restriction site.

Chemical biotinylation of BSA and eGFP

Investigator: Julian

Procedure:

1 g BSA was chemically biotinylated with a 40x molar excess of biotin-NHS-ester:

100 ml of 50 mM borate buffer with 50 mM NaCl pH 8.85

dissolve BSA (10 mg/ml)

add adequate amount of biotin-NHS-ester: 205 mg

reaction for approx. 45 minutes at RT after full dissolving of biotin-NHS-ester

store at 4 °C

eGFP was chemically biotinylated with a 16x (error in calculations) molar excess of biotin-NHS-ester:

eGFP in 75 ml of 50 mM borate buffer without NaCl pH 8.85

1to10 dilution: extinction(280) = 0.371

add adequate amount of biotin-NHS-ester: 69 mg

reaction for approx. 45 minutes at RT after full dissolving of biotin-NHS-ester

store at 4 °C

Next Steps

add another 104 mg of biotin-NHS-ester incl. reaction at RT tp reach desired 40X molar excess
Purification via column chromatography

Week 12, August 1st - August 7th

Monday, August 01

Cloning of Streptavidin/Streptactin/Traptactin from GSY5 and GSY6 into pASK75 + Transformation

Investigator: JB

PCR products from GSY5 and GSY6 were, after digestion overnight with Nde1, loaded on an 1.8% agarose gel. The fragment bands at roughly 350 bps were extracted.

Digested pASK75 (P202 and P203 dig. with Nde1) were loaded onto an 1% agarose gel, the vector fragments at 3800 bp isolated and purified.

Vector fragment plus Streptavidin fragments were ligated and transformed into XL-1 blue

-> F159+F160, F159+F161

Cloning of EGFR-TMD - mRuby - Strep with IRES-BirA

Investigator: JB

2 µg of P77 (EcoRI, XbaI) and P199 (EcoRI, SpeI) were digested for 2 hours at 37°C
Digestions were separated on a 1% agarose gel, fragments corresponding to the vector (P77) and to the to be cloned insert (P199) were isolated and purified
Ligation of inserts for 30 mins at RT
Transformation of ligation into XL1-blue

Retrafos of cell culture constructs for signal peptide testing for midipreps

Investigator: JB

Retransformation of all constructs in XL1-blue
Constructs concerned are: P152, P171, P205 (Nanoluc-constructs) and P201, P208 and P211 (mRuby-constructs)
Transformation according to protocol, plates incubated at 37°C overnight

Tuesday, August 02

Wednesday, August 03

Verification of cloning P210 (CMV-IgKappa-Nanoluc-StrepTag-PolyA)

Investigator: Niklas

Aim of the experiment: Verification of successful cloning after sequencing showed that the last part of the construct might be missing

Procedure:

digestion with AgeI and PstI (sample was digested with EcoRI and PstI for 10 minutes, than inactivated an ligated)

Results:

the gel shows a band at about 3500 bp (pSB1C3 + full insert)
gel shows additionally a band below 750 bp (CMV+ IgKappa)
the sample contains the full insert as well as the small insert (CMV+IgKappa without Nanoluc-StrepTag-PolyA)
cloning not succesful
the construct was inocculated from plate again

Transformation of E. coli XL1 blue with Ligations F159 + F160 and F159 + F161 (pASK + streptavidin from GSY 5 and 6)

Investigator: Niklas

Aim of the experiment: Transformation of E. coli XL1 blue.

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37 °C in the incubator.

Thursday, August 04

MidiPrep P152 and P171 (pSB1C3)

Investigator: EF

Aim of the experiment: isolate Plasmids

Procedure:

MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen). After washing the DNA with 70% Ethanol the pellet was left in special centrifugation tubes (labeled 152+QF; 171+QF) in order to air-dry. EB buffer for storage was later added by CG.
Conc: 1000 ng/ul

Cloning of BAP Nanoluc (P206) before A3C5 (P213)

Investigator: NA

Procedure:

Preparative digestion:

P213 (A3C5): EcoRI and NgoMIV -> F170

P206 (BAP Nanoluc): EcoRI and AgeI -> F171

Both fragments were ligated after gelextraction.

CaCl2 competent E. coli XL1-Blue cells were taken out of stock in -80 °C freezer and were gently thawed on ice.

7 µl of Ligation was added to 100 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 750 µl LB-medium to each tube.

Incubation for 1 hour at 37 °C

The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C in the cell-culture shaker.

results: Gelextraction:

the plates showed no colonies. repeat

Friday, August 05

Verification of successful cloning of all Streptavidin variants into pASK75

Investigator: CG

Aim of the experiment: Minipreps von pASK75 Streptavidin variants (codon optimzied Streptavidin, Streptactin, Traptactin)

Procedure:

MiniPrep was performed according to the manufacturer's protocol (QIAprep MiniPrep, Qiagen) for 3 clones of GSY5 and 6 clones of GSY6

Analytic digestion with 0.25 µL NdeI, 0.25 µL HindII, 1 µL SmartCut Buffer, 200 ng plasmid DNA, H₂O to 20 µl

10 µL on 1% agarose gel electrophoresis

Results: Successful cloning was verified for all plasmids by analytical digestion. Expected and observed fragment size for the vector was 3.1 kb and about 350 bp for the inserts. 4 plasmids were sent for sequencing (1x GSY5, 3x GSY6). Alle sequences were error-free. Therefore all 3 Streptavidin variants are available now.

Transformation of: Streptavidin variants, PAS-Plasmid, Interlab-Plasmids, Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA and Ligation of BAP-Nanoluc-A3C5

Investigator: CG

Aim of the experiment: Transformation of Streptavidin variants, PAS-Plasmid, Interlab-Plasmids into E. coli BL21 and Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA, Ligation of BAP-Nanoluc-A3C5 in E. coli XL1 blue

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

7 µl of Ligations mixes were added to 50 µl of competent cells and gently mixed, 1 µl for ccc Plasmids

30 min incubation on ice

1 min. heat shock at 42 °C

Adding of 950 µl LB-medium to each tube, and incubation for 1 h at 37°C

The cell suspension was plated on ampicillin plates (inclusive rescue plate) / CamR- plates and incubated for 7 h at 37 °C in the programmed incubator.

Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA and Ligation of BAP-Nanoluc-A3C5

Investigator: CG

Aim of the experiment: Re-Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA, Re-Ligation of BAP-Nanoluc-A3C5

Procedure:

The corresponding Fragments were mixed with 2 µl Ligase-buffer, 1 µl T4-Ligase and filled with water up to 20 µl

7.3 µl F163 + 2.7 µl F162 (=F173)

3.7 µl F170 + 6.3 µl F171 (=F174)

The Ligation mixes were incubated for 1 h at room temperature.

SDS Page of Streptavidin production

Investigator: CG

Aim of the experiment: Verification of successful Streptavidin production and preperation for the data package

Procedure: Streptavidin samples from the production process were further processed with SDS buffer. Some samples had very few volume, therefore the overall volume was reduced. For informations on the samples content please refer to NA. The low volume might be a problem due to evaporation issues.

Sample 1: the tube was empty
Sample 2: 1 µl sample was mixed with 7 µl water and 2 µl SDS buffer
Sample 3: 80 µl sample was mixed with 20 µl SDS buffer
Sample 4: 80 µl sample was mixed with 20 µl SDS buffer
Sample 5: 20 µl sample was mixed with 5 µl SDS buffer
Sample 6: 80 µl sample was mixed with 20 µl SDS buffer
Sample 7: 80 µl sample was mixed with 20 µl SDS buffer
Sample 8: 80 µl sample was mixed with 20 µl SDS buffer
Sample 9: 80 µl sample was mixed with 20 µl SDS buffer

10 µl of each sample were loaded on the pre-mixed SDS gel.

Gel 1: 8 µl Ladder, samples 1-6

Gel 2: 8 µl Ladder, samples 7-9, 5 µl of samples 7-9

The gel ran at 160 V for about 1 1/2 h. Afterwards it was incubated for 30 min. in staining solution, 10 min. in destaining solution 1 and over the weekend in destaining solution 2.

Results:

Week 13, August 8th - August 14th

Monday, August 08

PCR, Purification and digestion of BirA

Investigator: LK

Aim of the experiment: Amplification of BirA

Procedure:

PCR according to the SOP (primers: O17 and O18, Annealing at 62°C)
PCR purification via the purification kit according to the manufacturer's protocol
preparative digestion with XbaI and PstI over night in a 50µl batch

Results:'

Concentration after PCR-purification: 116ng/µl
Gel: One thick band at ~1000Bp --> BirA and one at ~2100Bp --> vector, we're cut out and purified via the Gelextraction kit according to the manufacturer's protocoll.
Concentrations: BirA (F186) : 62,5 ng/µl, pSB1C3 (F187): 32,5 ng/µl

Determination of Streptavidin concentration

Investigator: NA

Procedure:

OD280 measurement with quartz cuvette

result: the 1:100 dilution showed an OD of 0,469

Calculation with extinction coefficient (expasy tool) of 41940 M ^-1 * cm ^-1 and 13.3 kDA as molar mass of streptavidin monomer provides concentration below:

14.87 mg/mL

Inocculation of Streptavidin (wild type, P235) in M9 medium for fermentation

Investigator: NA

Procedure:

M9 medium with Amp (1:1000) is inocculated with preculture (~50 mL) of P235

the culture is incubated in the shaker over night at 37°C

PCR purification

Investigator: EF

Aim of the experiment: Purificate bands for blunt ligation in F113

Seeding of HEK293T cells in cell culture

Investigator: JB

Aim of experiment:

Thawing and seeeding of HEK293T cells for experiments later this week

Procedure:

Tube with cells was thawed quickly in a 37°C waterbath

After bringing most of the cell suspension in a fluid state, the suspension was transferred into a 50 ml Falcon tube and suspended in 50 ml of RPMI1640 medium (with 10% CFS and Pen/Strep added).

Cells were spun down for 2 mins at 2,300 rcf and the pellet resuspended in 20 ml of medium in order to remove residual DSMO from the cells (DSMO having been used for freezing the cells).

The resuspended cells were transferred into a culture flask and incubated overnight at 37°C/5% CO².

Cloning of IgKappa signale peptide, PAS-Lysin and further constructs for the receptor

Investigator: CG

Aim of experiment:

Cloning of CMV-IgKappa+Nanoluc-Strep-PolyA, BAP-Nanoluc+A3C5, IRES-BirA + polyA and Sumo-PAS-Lysin into pASK75

Procedure:

Digestion of 3 µg of each plasmid in 30 µl mix:

20 µl P205 (CMV-IgKappa) with EcoRI, AgeI -> Gel 1, left lane, expected fragment at about 600 bp -> F175
15 µl P160 (Nanoluc-Strep-PolyA) with EcoRI, NgoMiV -> Gel 1, right lane, expected fragment at about 3000 bp -> F176
20 µl P212 (A3C5) with EcoRI, NgoMiV -> Gel 2, left lane, expected fragment at about 2.200 bp -> F177
10 µl P206 (BAP-Nanoluc) with EcoRI, AgeI -> Gel 2, right lane, expected fragment at about 500 bp -> F178
10 µl P199 (EGFR-TMD-mRuby-Strep) with EcoRI, SpeI -> Gel 3, left lane, expected fragment at about 1.500 bp -> F179
20 µl P236 (PAS-Lysin-Sumo) with NdeI, HindIII -> Gel 3, right lane, expected fragment at about 1.000 bp -> F180
10 µl P77 (IRES-BirA-KDEL) with EcoRI, SpeI -> Gel 4, left lane, expected fragment at about 1000 bp -> F181

Ligation in 20 µl mix (s. above fragment names):

F182: 2.9 µl F176 + 7.1 µl F175
F183: 5.2 F177 + 4.8. F178
F184: 7.0 µl F159 + 3.0 µl F180
F185: 2.9 µl F133 + 7.1 µl F181

Transformation according to SOP.

Results:

For all ligations colonies grew the next day.

Gel 1:

Gel 2:

Gel 3:

Gel 4:

Tuesday, August 09

Transformation of Biobricks in NEB Turbo

Investigator: Julian

Aim of the experiment: Acquisition of pBAD/AraC and Lox site

Procedure:

resuspend DNA with 10 µl ddH2O in well of interest (standard distribution kit)
incubate for 5 min
transformation of 1 µl plasmid according to SOP in NEB Turbo

Used bricks: BBa_I0500 and BBa_J61046

Inoculation and induction of AraC+pBAD controlled eGFP production in E.coli BL-21

Investigator: LK

Aim of the experiment: Confirmation of arabinose dependend activation of the pBAD-promotor in AraC-Operon.

Procedure:

E.coli Bl-21 with P61 (PC+AraC+pBAD+eGFP in pSB1C3) we're picked and a 4ml preculture (LB+cam) was inoculated and incubated for 6h.
According to the following table 50ml cultures (LB+cam) we're incoculated with 500µl of the preculture and incubated over night at 37°C.

Arabinose concentration:

negative control

100mM

10mM

1mM

100µM

10µM

Results:

Cloning of F186 (BirA) into F187 (pSB1C3)

Investigator: LK

Aim of the experiment: Getting the BirA for the prokaryotic receptor.

Procedure:

1,7µl of F187 and 6,3µl of F186 we're ligated for 1h at RT accoridng to the SOP. --> F189
The ligation-batch was transformed into NEB-Turbo cells and plated out on cam-plates. Incubation at 37° o/n.

Inoculation of precultures from Ligations F182-F185

Investigator: LK

Aim of the experiment: Getting plamids of CMV-IgKappa+Nanoluc-Strep-PolyA (F182), BAP-Nanoluc+A3C5 (F183),Sumo-PAS-Lysin (F184) and IRES-BirA + polyA (F185)

Procedure:

Inoculation of 4mL cultures (LB cam resp. amp (F184)). Incubation at 37°C o/n.

Inocculation of fermenter

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

centrifuge preculture (P235 in M9 medium)
resuspend pellet in HCDF medium and inocculate fermenter (HCDF medium)
pO₂= 60 %; Temp= 30°C, pH~7
growth over night

SDS Page of Streptavidin production

Investigator: NA

Aim of the experiment: Verification of successful Streptavidin production and preperation for the data package

Procedure: Streptavidin samples from the production process were further processed with SDS buffer. Some samples had very few volume, therefore the overall volume was reduced.

1: 8 µl Ladder
2: 10 µl after induction (1 µl sample was mixed with 7 µl water and 2 µl SDS buffer)
3: 5 µl supernantant after denaturation (20 µl sample was mixed with 20 µl H₂O and 10 µl SDS buffer)
4: 5 µl before precipitation(80 µl sample was mixed with 20 µl SDS buffer)
5: 10 µl supernantant after 40% precipitation (80 µl sample was mixed with 20 µl SDS buffer)
6: 10 µl supernantant after 70% precipitation (80 µl sample was mixed with 20 µl SDS buffer)
7: 10 µl after dissolving in 2.2M (NH₄)2SO₄ (80 µl sample was mixed with 20 µl SDS buffer)

The gel ran at 145 V

Results:

Transformation of F192 and P238

Investigator: NA

Procedure:

CaCl2 competent E. coli XL1-Blue cells were put out from the stock in -80 °C freezer and were gently thawed on ice.

7 µl of DNA was added to 50 µl of competent cells and gently mixed.

30 min incubation on ice

5 min. heat shock at 37 °C

Adding of 950 µl LB-medium to each tube.

The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37 °C.

Wednesday, August 10

Minipreps and analytical digestion of P237 - P243

Investigator: LK

Aim of the experiment: Isolating and verifiing plamids of CMV-IgKappa+Nanoluc-Strep-PolyA (F182), BAP-Nanoluc+A3C5 (F183),Sumo-PAS-Lysin (F184) and IRES-BirA + polyA (F185)

Procedure:

Minipreps were performed according to the manufacturer's protocol.
~200- 500ng of ach Plasmid (accept P241) were digested with EcoI and PstI for 45 min. and a gel-elctrophoresis (1% Agarose) of the digestion-batches was performed.

Results:

* P237: expected band for CMV-IgKappa+Nanoluc-Strep-PolyA at ~1850 Bp , but unexpected band at ~1100. Discard sample? 
* P238: expected band for CMV-IgKappa+Nanoluc-Strep-PolyA at ~1850 Bp 
* P239 and P240: expected band at ~650 Bp 
* P242 and P243: bands at ~2000 Bp. Digested vector and Fragment are not distinguishable --> sequencing

Cloning constructs for the eukaryotic and prokaryotic receptor

Investigator: CG

Aim of experiment:

Cloning of EGFR-TMD-mRuby-Strep-IRES-BirA-KDEL-PolyA, BAP-Nanoluc-A3C5-EspP-2xTerm

Procedure:

Digestion of 3 µg of each plasmid in 30 µl mix:

6 µl P242 (IRES-BirA-KDEL-PolyA) with EcoRI, XbaI -> Gel 1, left lane, expected fragment at about 4000 bp -> F190
20 µl P108 (EspP-Termin.) with EcoRI, NgoMiV -> Gel 1, right lane, expected fragment at about 3000 bp -> F191

Ligation in 20 µl mix (s. fragment names above):

F192: 4 µl F190 + 6 µl F179

Transformation according to SOP.

Results:

Gel 1:

Transformation of P22; P67; P122; P137; P160

Investigator: MT

Aim of the experiment:

Amplification of P22; P67; P122; P137; P160

#	Plasmid	Description
P22	K157001	RFP-Gen.(Retrafo P4)
P67	pSB1C3	EGFR signal peptide (transloc. pore)
P122	pSB1C3	Ig Kappa (digest. GSY3)
P137	pSB1C3	T7/BM40 aus GSY
P160	pSB1C3	NanoLuc + StrepTag + Poly-A

Procedure:

Transformation following SOP(13.02.2013)

Fermentation

Investigator: NA

Aim of the experiment: Streptavidin production

Procedure:

exponential feed (glucose, MgSO₄, Thiamin, Amp, HCDF salt, micronutrients) for ~13 h (about 3-4 L)
Induction of streptavidin expression (anhydro tetracyclin) at OD= 111.2
production over night

Thursday, August 11

Minipreps and analytical digestion of BBa_I0500 (AraC+ pBAD), BBa_J61046 (LoxP) and F189 (BirA)

Investigator: LK

Aim of the experiment: Isolating and verifiing the plasmids.

Procedure:

The Preperation was performed according to the manufacturer's protocol.
Each plasmid was digested with EcoRI and PstI and a gel-elctrophoresis (1% Agarose) of the digestion-batches was performed.

Results:

BBa_I0500 (AraC+ pBAD) = P246 and P247: Band at ~1250; Cloning was succesful
BBa_J61046 (LoxP) = P244 and P245: Fragment is too small (34Bp), not visible on gel.
F189 (BirA) = P248: Band at ~ 1000Bp; Cloning was succesful

Cloning of Streptavidin-variants into pASK111

Investigator: JB, LK, CG

Aim of experiment:

Cloning of Streptactin, Traptavidin, Streptavidin into CamR pASK111

Procedure:

Digestion of about 2.5 µg of each plasmid in 30 µl mix:

25 µl P233 (Streptavidin) with XbaI, HindIII -> Gel 1, left lane, expected fragment at about 400 bp -> F195
25 µl P231 (Traptavidin) with XbaI, HindIII -> Gel 1, right lane, expected fragment at about 400 bp -> F196
15 µl P241 (PAS-Lysin) with XbaI, HindIII -> Gel 2, left lane, expected fragment at about 400 bp -> -
25 µl P229 (Streptactin) with XbaI, HindIII -> Gel 2, left right, expected fragment at about 400 bp -> F197
15 µl P249 (pASK111) with XbaI, HindIII -> Gel 3, left lane, expected fragment at about 3000 bp -> F198

Ligation in 20 µl mix overnight (s. fragment names above):

F199: 3.7 µl F195 + 6.3 µl F198
F200: 5.4 µl F196 + 4.6 µl F198
F201: 4.1 µl F197+ 5.9 µl F198

Transformation according to SOP.

Results:

Gel 1:

Gel 2:

Gel 3:

Testpolymerization: BSA-coating

Investigator: EU, JH

Aim of experiment:

Coating of 6-well plate with BSA according to a modified ELISA-protocol.

Procedure:

Bicarbonate/carbonate coating buffer (100mM): 30,3 mg Na2CO3 60 mg NaHCO3 10 ml distilled water

"Blocking" Buffer: 1% BSA in PBS

Each well was covered with 0,5 ml BSA buffer and 0,5 ml bicarbonate buffer. After overnight incubation at RT, solution in wells was aspirated one by one and streptavidin was added. After a short incubation, the streptavidin(&Tris/HCl) solution was aspirated and Biotin solution was added (by needle).

1. well: 200 µl Streptavidin (11,2 mg/ml) + 200 µl Biotin, 2. well: 400 µl Streptavidin and 400 µl Tris/HCl + 200 µl Biotin, 3. well: 500 µl Streptavidin and 500 µl Tris/HCl + 300 µl Biotin, 4. well: 500 µl Streptavidin + 10 µl Biotin (this time with 2,5 µl pipette)

Results:

Overall polymerization was observed again, although it seemed more like an aggregation than a polymerization. No coating was observed except in the 4. well. Biotin-injection speed may be the critical point.

Poly-D-Lysine coating will follow as next step.

Transformation of P64; P73

Investigator: MT

Aim of the experiment:

Amplification of P22; P67; P122; P137; P160

#	Plasmid	Description
P64	pSB1C3	VEGF-p2a-PDGF
P73	pSB1C3	Poly-A

Procedure:

Transformation following SOP(13.02.2013)

Over night liquid culture of P22; P67; P122; P137; P160

Investigator: EF, MP

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

harvesting streptavidin

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

OD= 174
centrifuge culture
freeze pellet

SDS PAGE Streptavidin fermentation

Investigator: NA

Aim of the experiment: Verification of successfull production

Procedure:

according to protocol
8 µl Ladder; before induction; after induction
both samples: 3 µl culture + 77 µl TB + 20 µl SDS buffer; 12 µl on SDS gel

Results:

The fermentation was not successful, streptavidin band (unter 15 kDa marker) is just a bit thicker. The reason might be the ampR of the transformed plasmid. Due to the high cell concentration beta lactamase (secreted in periplasma) gets in the medium and hydrolyses amp. As a result cells lose plasmid because there is no selective pressure without an antibiotic in medium.

next step: cloning pf streptavidin mutants into pASK111 (camR)

Sequencing of P238, P245, P248

Investigator: NA

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer) - all samples: VF2
barcodes in stock list

Friday, August 12

PCR of Gensythesis (GSY) 7 and 8

Investigator: MT

Aim of the experiment:

Amplification of GSY 7 and 8

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	25 µL reaction	Final concentration
5X Q5 Reaction Buffer	5 µL	1 X
10 mM dNTPs	0.5 µL	200 μM
10 μM Forward Primer (D20)	1.25 μl	0.5 μM
10 μM Reverse Primer (VR)	1.25 μl	0.5 μM
Template DNA	1 µL	10 ng
Q5 High-Fidelity DNA Polymerase	0.25 μl	0.02 U/μl
Nuclease-Free Water	to 25 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	5 - 10 sec
	61 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	16 °C

Note: Use of the NEB T m Calculator is highly recommended.

Results:

After running on 1 %agarose gel only the 2kb bands belonging to GSY8 could be distinguished. These were extracted from the gel.

-> Repeat PCR for GSY7

Gelextraction of GSY8

Investigator: EF

Aim of the experiment: Gelextraction of 2kb band of PCR belonging to GSY8 Procedure:

Gelextraction was performed by manufacturers protocol (SLG).

Concentration:

7,7 ng/ul

Plasmid preparation of liquid culture of P22; P67; P122; P137; P160

Investigator: MP

Aim of the experiment:

Purification of P22; P67; P122; P137; P160

#	Plasmid	Description
P22	K157001	RFP-Gen.(Retrafo P4)
P67	pSB1C3	EGFR signal peptide (transloc. pore)
P122	pSB1C3	Ig Kappa (digest. GSY3)
P137	pSB1C3	T7/BM40 aus GSY
P160	pSB1C3	NanoLuc + StrepTag + Poly-A

Procedure:

According to Mini-prep kit, SLG

Results:

P22 ->P1001 103.6 ng/µL
P67 ->P1004 92.9 µL
P122 -> P1000 80.8 ng/µL
P137 -> P1003 87.9 µL
P160 -> P1002 100 ng/µL

Dephosphorylation of F113[HincII digested]

Investigator: MP, EF

Aim of the experiment:

Dephosphorylation of F113[HincII digested] (RFP-Reportercassette )

Procedure: According to NEB online Protocol for Dephosphorylation of 5 ́-ends of DNA using Antarctic Phosphatase (M0289):

12 µL F113 (85.1 ng/µL)
2 µL Antarctic Phosphatase Rxn Buffer (10X)
1 µL Antarctic Phosphatase (5000 u/mL)
5 µL ddH2O

Midiprep P238 (CMV-IgKappa-Nanoluc-Strep-polyA)

Investigator: NA

Procedure:

MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)

Results:

P253 - concentration: 2134 ng/µl

=== Digestion, Gel extraction and ligation of F1000 (P122), F1001 (P67), F1002 (P160) and F1003 (P137) ===

Investigator: EU

Aim of the experiment:

Preparation of plasmids

Procedure:

33 µL DNA
1 µL enzyme 1
1 µL enzyme 2
5 µL cut smart buffer
10 µL ddH20

Enzymes used:

F1000: AgeI + PstI
F1001: AgeI + PstI
F1002: NgoMiT + PstI
F1003: AgeI + PstI

Gelextraction:

Using gelextraction kit, Quiagen

Ligation

2µl F1000 + 6µl F1002
2µl F1001 + 6µl F1002
2µl F1003 + 6µl F1002

+ 1µl T4 Ligase and 1 l T4 ligase buffer for each ligation

Results:'

Left to right F1002(2x), F1001(2x), F1000(2x) and F1003(1x)

F1000 30 ng/µL
F1001 23,8 ng/µL
F1002 9,4 ng/µL
F1003 23,1 ng/µL

Saturday, August 13

Miniprep of pASK111 (empty) and diegestion

Investigator: LK

Aim of the experiment: Amplification of pASK111 and digestion for further ligation with SUMO-PAS-Lysin.

Procedure:

The Miniprep was performed according to the manufacturer's protocol.
The whole DNA was diegested with XbaI and HindIII. Over night at 37°C.
Gelelectrophoresis was performed and showed a significant band at ~2700.

Comment

Gel-ectraction has yet to be done .
equally digested insert from P236 was visible on gel. --> no ligation possible.

Transformation of F1006; F1007; F1008

Investigator: MT

Aim of the experiment:

Amplification of F1006; F1007; F1008

#	Ligation	Plasmid	Description
F1006	F1000 + F1002	pSB1C3	Ig Kappa + NanoLuc + StrepTag + Poly-A
F1007	F1003 + F1002	pSB1C3	T7/BM40 + NanoLuc + StrepTag + Poly-A
F1008	F1001 + F1002	pSB1C3	EGFR + NanoLuc + StrepTag + Poly-A

Procedure:

Transformation following SOP(13.02.2013)

Digestion and gelextraction of P64; P73

Investigator: JB, MT

Aim of the experiment:

Preparation for ligation

Procedure:

10 µL DNA
1 µL enzyme 1
1 µL enzyme 2
2 µL buffer
6 µL ddH20

Enzymes used:

P64: EcoRI + SpeI
P73: EcoRI + XbaI

Gelextraction:

Using gelextraction kit, Quiagen

Results:'

Left: P64 Right: P73

P64 -> F1011 14,2 ng/µL
P73 -> F1012 17,6 ng/µL

Sunday, August 14

Miniprep of P199-P201 and analytical digestion

Investigator: LK

Aim of the experiment: Isolation of "Streptavidin-variants" in pASK111 for preinoculation tomorrow.

Procedure:

The Miniprep was performed according to the manufacturer's protocol.
~200ng where digested with XbaI and HindIII.

Results:

All samples showed significant bands at ~400 Bp.

Transformation of P199-201 into E.coli BL-21

Investigator: LK

Aim of the experiment: Introducing Strep-variants in pASK111 into BL-21 for further fermentation.

Procedure:

The cells were transformed according to the SOP with 1µl of DNA and after 1h of incubation in LB without antibiotics plated out on Cam-plates.

Miniprep of P113-P213 and analytical digestion

Investigator: LK Aim of the experiment: Isolation of "Streptavidin-variants" in pASK111 for preinoculation tomorrow.

Procedure:

The Miniprep was performed according to the manufacturer's protocol.
~200 ng were digested with EcoRI and PstI.

Results:

PCR of Gensynthesis (GSY) 7, 8

Investigator: MT

Aim of the experiment:

Amplification of GSY7

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491)
Different amounts of template DNA were used

Component	50 µL reaction	Final concentration
5X Q5 Reaction Buffer	10 µL	1 X
10 mM dNTPs	1 µL	200 μM
10 μM Forward Primer (D20)	2,5 μl	0.5 μM
10 μM Reverse Primer (VR)	2,5 μl	0.5 μM
Template DNA	1 µL	1 - 10 ng
Q5 High-Fidelity DNA Polymerase	0.5 μl	0.02 U/μl
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
40 cycles	98 °C	5 - 10 sec
	58 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Results:

PCR GSY8 successful.

-> Do it again for GSY 7!

Over night liquid culture of F1006; F1007; F1008

Investigator: MT

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Gelextaction of F1004

Investigator: MT

Aim of the experiment:

Procedure:

Using gelextraction kit, Quiagen

Results:'

long F1004 -> F1013 6,4 ng/µL
short F1004 -> F1014 1,1 ng/µL

Ligation F1012 + F1011

Investigator: MT

Aim of the experiment:

Ligation F1012 + F1011

#	Plasmind	Description
F1011		VEGF-p2a-PDGF
F1012	pSB1C3	Poly-A

Procedure:

3 µL F1012
6 µL F1011
2 µL buffer
1 µL T4 Ligase
8 µL ddH2O

Results:

F1015

Transformation of F1015

Investigator: MT

Aim of the experiment:

Amplification of F1015

#	Ligation	Plasmid	Description
F1015	F1011 + F1012	pSB1C3	VEGF-p2a-PDGF + poly-A

Procedure:

Transformation following SOP(13.02.2013)

Results:

No colonies. Do it again.

Week 14, Aug 15th - Aug 21st

Monday, Aug 15th

Analytical digestion of P251 and P252

Investigator: Clemens

Aim of the experiment: Verify cloning

Procedure:

1µL Plasmid was digested with 1µL of EcoRI and PstI
Digestions were incubated for 1h
Samples were seperated by gelelectrophoresis on a 1% agarose gel

Results:

Cloning seems to have worked

500px

Plasmidpreparation of liquid culture of F1006; F1007; F1008

Investigator: MP

Aim of the experiment:

Purification of F1006; F1007; F1008

#	Plasmid	Description
F1006	pSB1C3	Ig Kappa + NanoLuc + StrepTag + Poly-A
F1007	pSB1C3	T7/BM40 + NanoLuc + StrepTag + Poly-A
F1008	pSB1C3	EGFR + NanoLuc + StrepTag + Poly-A

Procedure:

According to Mini-prep. kit, Quiagen

Results:

F1006 -> F1005 83.2 ng/µL
F1007 -> F1006 91.8 ng/µL
F1008 -> F1007 367.1 ng/µL

Cloning of Nanoluc-Strep in front of double terminator and PAS-Lysine into pASK111

Investigator: LK, CG

Aim of experiment:

Cloning of Nanoluc-Strep in front of double terminator and PAS-Lysine into pASK111

Procedure:

Plasmid preperation according to SOP of P264, P265

Digestion of about 3 µg of each plasmid in 30 µl mix:

6 µl P29 (double teminator) with EcoRI, XbaI -> Gel 1, left lane, expected fragment at about 3000 bp -> F207
15 µl P98 (Nanoluc-Strep) with EcoRI, SpeI -> Gel 1, right lane, expected fragment at about 500 bp -> F208
15 µl P264 (PAS-Lysin) with XbaI, HindIII -> Gel 2, left lane, expected fragment at about 1000 bp -> F210

Ligation in 20 µl mix for 30 min. at room temperature (s. fragment names above):

F209: 3.7 µl F207 + 6.3 µl F208
F211: 1.1 µl F210 + 8.9 µl F206

Transformation according to SOP.

Results:

Gel 1:

Gel 2:

Tuesday, Aug 16th

Over night liquid culture of P64; P73

Investigator: MP

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Gelextraction of PCR GSY8(Saturday, August 13)

Investigator: EF

Aim of the experiment:

Purification of PCR GSY8(Sunday, August 14)

Procedure:

Using gelextraction kit, SLG

Results:

F1016 3,4 ng/µL

Seeding of HEK293T cells for transfection

Investigator: LK, CG

Aim of the experiment:

3x4 petri dishes with HEK293T cells for performing the Nanoluc assay in order to validate the signale peptides

Procedure:

Washing each T75 flask with 10 ml PBS
Centrifugation for 10 min. at 1.8 rcf
Resuspending the cell pellet in 10 ml medium
Counting the cells (33x10^6 cells in 10 ml)
Plating 0.5x10^6 cells onto petri dishes in 10 ml medium an 1x10^6 onto a T75 flask
Incubation for 2 days

Results:

ready to transfect cells in petri dishes

Gelextraction of PCR GSY8(Saturday, August 13)

Investigator: MP

Aim of the experiment:

Purification of PCR GSY8(Sunday, August 14)

Procedure:

Using gelextraction kit, SLG

Results:

F1016 3,4 ng/µL

Transformation of F1015

Investigator: MT

Aim of the experiment:

Amplification of F1015

#	Ligation	Plasmid	Description
F1015	F1011 + F1012	pSB1C3	VEGF-p2a-PDGF + poly-A

Procedure:

Transformation following SOP(13.02.2013)

PCR of Gensynthesis (GSY) 7

Investigator: EF

Aim of the experiment:

Amplification of GSY7

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491)
Reactions with and without GC Enhancer were performed

Component	50 µL reaction x 6	Final concentration
5X Q5 Reaction Buffer	10 µL	1 X
10 mM dNTPs	1 µL	200 μM
10 μM Forward Primer (D20)	2,5 μl	0.5 μM
10 μM Reverse Primer (VR)	2,5 μl	0.5 μM
Template DNA	1 µL	1 ng
Q5 High-Fidelity DNA Polymerase	0.5 μl	0.02 U/μl
5X Q5 High GC Enhancer (optional)	5 µL	1X
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
40 cycles	98 °C	5 - 10 sec
	58 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	16 °C

Results:

negativ. Two 1% agarose gels were performed to prove the PCR product. Both were negativ.

Precipitation of eGFP

Investigator: LK

Aim of experiment: Determination of (NH₄)₂SO₄ -concentration needed to precipitate eGFP.

Procedure:

50mL of eGFP solution (from fermentation) where gradually precipitated with rising concentrations (NH₄)₂SO₄ (step size: 400mM)
All steps where performed at 4°C.
Pellets where solved in 10 mL 1x PBS.

Results:

Extinction:

Maximum Absorption at 488nm for eGFP. Absorption coefficient(eGFP,488): 53000 mol/Lcm.

mM (NH₄)₂SO₄	Dilution	Extinction	Concentration eGFP [µM]
400	1:10	0,197	37,0
800	1:10	0,084	15,8
1200	1:10	0,457	86,2
1600	1:100	0,16	301,8
2000	1:100	0,375	707,5
2400	1:10	0,505	95,3
2800	1:10	0,08	15,0

Inocculation of P258_E.coli_Bl-21 in M9 medium for fermentation

Investigator: LK

Procedure:

M9 medium with Cam (1:1000) was inocculated with preculture (~50 mL) of P258 (pASK111+Streptavidin)

the culture was incubated in the shaker over night at 37°C

Phosphorylation of F1005; F1016

Investigator: MP

Aim of the experiment:

Phosphorylation of F1005; F1016

Procedure:

39 µL DNA
5 µL 10x T4 PNK Bufer
10 mM ATP
T4 PNK

Phosphorylation of O31; O32

Investigator: MP

Aim of the experiment:

Phosphorylation of O31; O32

Procedure:

0.5 µL Oligonucleotides (10µM)
2 µL 10x T4 PNK Bufer
2 µL 10 mM ATP
1 µL T4 PNK
14.5 µL H2O
95 °C; 3 min

Hybridization of phosphorylated O31; O32

Investigator: MP

Aim of the experiment:

Hybridization of phosphorylated oligonucleotides: O31; O32

Procedure:

2 µL O31
2 µL O32
200 µL ddH20
37 °C 20 min
75 °C 10 min

Wednesday, August 17

Gelelectrophoresis of GSY7

Investigator: EF

Aim of experiment: gelelectrophoresis of the remaining product of GSY7 PCR (from 16.8.16)

Procedure: Agarose gelelectrophoresis was performed using an increased amount of SYBR Green

Results There was no PCR product identified.

Plasmidpreparation of liquid culture of P64; P73

Investigator: MP

Aim of the experiment:

Purification of P64; P73

#	Plasmid	Description
P64	pSB1C3	VEGF-p2a-PDGF
P73	pSB1C3	Poly-A

Procedure:

According to Mini-prep. kit, SLG

Results:'

P64 134.4 ng/µL
P73 149.4 ng/µL

Over night liquid culture of F1015

Investigator: MP

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

PCR of scAvidin

Investigator: Julian

Aim: Extraction of single chain Avidin from vector for further cloning

Procedure:

reaction was performed after SOP (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
2 ng Plasmid were used for amplification (1 µL)
Primers: O-27 and O-28

PCR program (standard):

Step	Temperature [°C]	Time [s]
initial denaturation	98	120
35 cycles	98	10
	64	30
	72	300
final extension	72	300
Hold	4	ꝏ

Quickchange of P206 and P239 to correct BAP

Investigator: Julian

Aim: Quickchange P206 (BAP-NanoLuc) and P239 (BAP-NanoLuc-A3C5) to correct BAP

Procedure:

reaction was performed after SOP (PCR usingPfuUltra II Fusion HS DNA Polymerase, Agilent)
10 ng Plasmid were used for amplification (2.5 µL)
Primers: O-33 and O-34

Step	Temperature [°C]	Time [s]
initial denaturation	98	120
35 cycles	98	10
	55	30
	68	300
final extension	68	360
Hold	4	ꝏ

Inocculation of fermenter

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

centrifuge preculture (P258 in M9 medium)
resuspend pellet in HCDF medium of fermenter and inocculate
pO₂= 60 %; Temp= 37°C, pH~7
growth over night

Thursday, Aug 18th

PCR of gene synthesises 8 with Q5 polymerase

Investigator: EF

Aim of the experiment: Amplification of GSY7 with optimized Tm following negativ PCR reactions in order to amplify GSY7. Procedure: Approach:

2,5 µl forward Primer VF2
2,5µl reverse Primer VR
1µl dNTPs
1µl DNA (1ng)
10µl 5x Q5-Puffer
0,5µl Q5-Polymerase
Fill up with water up to 50 µl

Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)

98°C_2min initiation step
98°C_10sec
62°C_30sec > step 2-4: 35 repeats
72°C_1min
72°C_5min final step
4°_hold

PCR of gene synthesises 8 with Pfu Ultra II polymerase

Investigator: EF

Aim of the experiment: Amplification of GSY7 with Pfu Ultra II polymerase following negativ PCR reactions in order to amplify GSY7. Procedure: Approach:

2,5 µl forward Primer VF2
2,5µl reverse Primer VR
1µl dNTPs
1µl DNA (1ng)
10µl Pfu Ultra II-Puffer
0,5µl Q5-Polymerase
Fill up with water up to 50 µl

Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)

98°C_2min initiation step
98°C_10sec
56°C_30sec > step 2-4: 35 repeats
72°C_2min
72°C_5min final step
4°_hold

Fermentation

Investigator: NA

Aim of the experiment: Streptavidin production

Procedure:

exponential feed (Cam) for ~13 h (about 3-4 L); start at OD= 11.66
Induction of streptavidin expression (anhydro tetracyclin) at OD= 119
change of settings: pO2= 40 %; Temp= 30°C, pH~7
production over night

Streptavidin production in shaking flask

Investigator: NA

Aim of the experiment: Streptavidin production

Procedure:

2 L LB medium (Cam 1:1000) was inocculated with ~10 ml M9 preculture (P258 in BL21)
induction with anhydro tetracycline (200µl, 2 mg/ml) at OD= 3,32
culture was incubated at 37 °C and 140 rpm for 4 hours
after expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
the supernatant was discarded, and the pellet was frozen away

Transformation of quickchanged P239 and 206 (BAP_Nanoluc_A3C5 and BAP_Nanoluc)

Investigator: LK

Procedure:

After DpnI-digestion 10µl of each plasmid was transformed into E.coli XL-1-blue.
Cells where plated out an Cam-plates after 1h of incubation without antibiotics.

MiniPrep of F209 to P266 and P267, analytic digestion

Investigator: JL

Aim of the experiment: Verification of successful cloning.

Procedure: MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)

Concentrations:

Plasmid	c [ng/µl]
P266	198
P267	200,8

Analytic digestion: 0.5 µl PstI, 0,5 µl EcoRI, 1 µl CutSmart, 6 µl ddH2O for P266 and P267 for 2 h at 37°C.
1% agarose gel electrophoresis.

Results:

Lane 1: 10 µl 1 kb Ladder.
Lane 2: Digest of F209 to P266.
Lane 3: Digest of F209 to P267.

Phosphorylation of O31; O32

Investigator: MP

Aim of the experiment:

Phosphorylation of O31; O32

Procedure:

5 µL Oligonucleotides (µM)
2 µL 10x T4 PNK Bufer
2 µL 10 mM ATP
1 µL T4 PNK
10 µL H2O
95 °C 3min.

Hybridization of phosphorylated O31; O32

Investigator: MP

Aim of the experiment:

Hybridization of phosphorylated oligonucleotides: O31; O32

Procedure:

2 µL O31
2 µL O32
200 µL ddH20

Plasmidpreparation of liquid culture of F1015

Investigator: MP

Aim of the experiment:

Purification of F1015

#	Plasmid	Description
F1015	pSB1C3	VEGF-p2a-PDGF + Poly-A

Procedure:

According to Mini-prep. kit, SLG

Results:'

F1015 -> P1008 256.6 ng/µL

Friday, Aug 19th

Gelelectrophoresis of GSY7

Investigator: EF

Aim of experiment: gel electrophoresis of repeated GSY7 PCR (from 18.8.16)

Procedure: Agarose gelelectrophoresis was performed at 90V

Results There was no PCR product identified.

harvesting streptavidin

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

OD= 181
centrifuge culture for 1 h at 4800 rpm
freeze pellet (2033 g)

SDS PAGE Streptavidin fermentation

Investigator: NA

Aim of the experiment: Verification of successfull production

Procedure:

according to protocol
8 µl Ladder; before induction; after induction; sample of shaking flask production after induction
all samples: 0.5/OD µl culture filled up with EB to 80µl + 20 µl SDS buffer; 10 µl on SDS gel

Results:

Clear bands of acetyl transferase (chloramphenicol resistance) in fermenter samples. Therefore cells kept plasmid. The streptavidin bands before and after induction do not differ. The fermentation was not succesful. The shaking flask sample however shows a brighter band for streptavidin.

Miniprep of F211 (pASK111(PAS Lys)), I739001 (Biobrick) and F206 (pASK111 vectorfragment)

Investigator: Clemens

Aim of the experiment: Miniprep of plasmids Procedure:

Miniprep was performed by manufacturers protocol (Qiaprep, Qiagen)
Plasmids were named:
- F211 a: P268
- F211 b: P269
- I739001 a: P270
- I739001 b: P271
- F206 a: P272
- F206 b: P273

Cloning of P260 in P261 and F215 in P74

Investigator: Clemens

Aim of the experiment: Digestion, ligation and transformation Procedure:

Transfection of HEK cells with P253, P225 and P226

Investigator: LK

Aim of the experiment: Transfecting HEK cells with vectors encoding 3 diffrent types of signal peptides for secretion.

Procedure:

HEK293 where cultured and seeded out on 12 cellculture dishes. (~5x10⁵ cells per dish)
Transfection was performed on day 3 after seeding (60-70% confluency)
10µg DNA of each signalpeptide mixed with 30µg PEI (polyenthylenimine) in ddH2O where incubated for 15 min and added to the cells, which where previously washed with PBS and covered (4mL) with optiMEM media. (Pen/Strep;No serum!)
After 4h of incubation at 37°C, 5% CO₂ the media was changed to RPMI (Pen/Strep; 5% FCS) again.

Picking of E. coli XL1 blue in quickchanged pSB1C3 in P239 and P206, Retrafo of P261 and P213

Investigator: JL

Procedure:

Quickchanged pSB1C3 in P239: Colonies were picked from Cam-plates.

Retrafo of P261 and P213: Colonies were picked from Cam-plates.

Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contains 4 mL of LB-medium + 4 µL of the proper antibiotic.

These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight

Repeat of PCR of scAvidin

Investigator: Julian

Aim: Extraction of single chain Avidin from vector for further cloning

Procedure:

reaction was performed after SOP (PCR Using Q5® High-Fidelity 2X Master Mix, NEB)
2 ng Plasmid were used for amplification
Primers: O-27 and O-28
annealing temperature was lowered to 60 °C

PCR program (standard):

Step	Temperature [°C]	Time [s]
initial denaturation	98	120
35 cycles	98	10
	60	30
	72	150
final extension	72	300
Hold	4	ꝏ

Repeat of PCR of Gene Synthesis 9

Investigator: Julian

Aim: Amplification of gensynthesis 9 for further cloning

Procedure:

reaction was performed after SOP (PCR Using Q5® High-Fidelity 2X Master Mix, NEB)
2 ng Plasmid were used for amplification
Primers: VF2 and VR

PCR program (standard):

Step	Temperature [°C]	Time [s]
initial denaturation	98	120
35 cycles	98	10
	61	30
	72	120
final extension	72	300
Hold	4	ꝏ

Preparative digestion of P8 (Streptavidin wt)

Investigator: Julian

Aim of experiment: preparation for cloning of SA1 into pASK111

Procedure:

preparative digestion batch

volume	reagent
40 µl	Plasmid DNA P8
5 µl	Cutsmart (10x)
1.5 µl	HindIII
1.5 µl	XbaI
2 µl	ddH2O
=50 µl	TOTAL

duration: over night

Saturday, Aug 20th

Miniprep and analytical digestion of P274-P277

Investigator: LK

Aim of the experiment: Isolating and verifiing A3C5+EspP_ddT ligation, "quickchanged" BAP-constructs and amplification of A3C5 in pSB1C3.

Procedure:

Minipreps where performed according to manufacturer's protocol.
Analytical digestion with EcoRI and PstI of ~ 200-250ng of each plasmid was performed for 30 min at 37°C.

Results:

Sunday, Aug 21st

Cloning of GSY9 and scAvidin

Investigaor: LK, JL

Procedure:

The PCR of scAvdin was digested over night with SpeI and NgoMIV at 37°C.
The PCR of GSY9 was divided: one half was digested with XbaI and AgeI (-> F224) and the other half was digested with XbaI and HindIII (->F225).
Additionally P74 (pSB1C3+RFP-Reporter) was digested with XbaI and AgeI (-> F227) to provide a plasmid for the ligation with F224.

The digestions where plotted on a gel, and bands at 1700Bp for scAvidin, 222Bp for TetO-OmpA, 490Bp for eMA and 2100Bp for pSB1C3 where cut out and purified with the Promega Wizard SV Gel Kit according to the manufactuerers protocol.

F224 (TetO-OmpA) was then ligated with F227 (pSB1C3), F225 (enhanced monomeric Avidin) was ligated with F206 (pASK111) and F226 (scAvidin) was ligated with F218 (pSB1C3). Ligations where incubated over night at 16°C.

Transformation was performed according to the SOP on Monday morning.

Week 15, Aug 22nd - Aug 28th

Monday, Aug 22nd

Sequencing of P268, P276, P277 and P279

Investigator: Julian

Aim of the experiment: Sequencing of P268 (PAS lysine), P276 (QC BAP-NanoLuc-A3C5), P277 (QC BAP-NanoLuc) and P279 (A3C5-EspP-DoubleTerminator)

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer)

P268 (D20) FR12904429
P276 (VF2) FR12904428
P277 (VF2) FR12904427
P279 (VF2) FR12904426

Analytical digestion of P278 (pSB1C3(A3C5-EspP-doubleterminator) & P279

Investigator: Clemens

Aim of the experiment: cofirm success of cloning

Procedure:

Batch for analytical digestion for P278/P279 with PstI-HF and EcoRI-HF

volume	reagent
2 µl/ 1 µl	Plasmid DNA P278/P279
1 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF (10 U/µl)
1 µl	PstI-HF (20 U/µl)
5 µl/ 6 µl	ddH2O
=10 µl	TOTAL

Results:

P279 showed the expected signal at 1100 bp

Ligations of F1013 + gsy7; +gsy8

Investigator: EF

Aim of the experiment: cloning for further ligation steps Procedure:

Tuesday, Aug 23rd

Inoculation of Precultures of F228, F229 and F230

Investigator: Clemens

Aim of the experiment: Prepare cells for Miniprep

Procedure:

Two colonies were picked from each plate
LB CAM was inoculated with F228 and F230
LB AMP was inoculated with F229
Precultures were incubated for 7 hours at 37°C

Results:

Each preculture showed cell growth

Miniprep of F228, F229 and F30

Investigator: Clemens

Aim of the experiment: Obtain plasmids

Procedure:

Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)

Plasmids were renamed:
- F228 1: P281
- F228 2: P282
- F229 1: P283
- F229 2: P284
- F230 1: P285
- F230 2: P286

Results:

Concetrations in "Inventarliste"

Digestion of IRES-construct (F1019) by PmeI+NotI

Investigator: EU

Aim of the experiment: Prepare construct for ligation later on

Procedure:

5 µl DNA 38µl ddH2O 1µl of each enzyme 5µl cut smart buffer

incubation at 37°C for 1 h Gel electrophoresis and gel extraction

Results:

Fragment was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.

Wednesday, Aug 24th

analytical digestion of P281, P282, P283, P284, P285 and P286

Investigator: Clemens

Aim of the experiment: Verify success of cloning

Procedure:

Batch for analytical digestion of P281/P282 with PstI-HF and EcoRI-HF

volume	reagent
1 µl/ 1 µl	Plasmid DNA P281/P282
1 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF (10 U/µl)
1 µl	PstI-HF (20 U/µl)
6 µl/ 6 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P283/P284 with XbaI and HindIII-HF

volume	reagent
1 µl/ 1 µl	Plasmid DNA P283/P284
1 µl	Cutsmart buffer (10x)
1 µl	XbaI
1 µl	HindIII-HF
6 µl/ 6 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P285/P286 with PstI-HF and EcoRI-HF

volume	reagent
1 µl/ 1 µl	Plasmid DNA P285/P286
1 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF (10 U/µl)
1 µl	PstI-HF (20 U/µl)
6 µl/ 6 µl	ddH2O
=10 µl	TOTAL

Digestions were incubated at 37° for 1h

Results:

PCR of Genesynthesis 9 with VF2 and VR

Investigator: Clemens

Aim of the experiment: Amplification of GSY9

Procedure:

reaction was performed after SOP (Q5 Hotstart, NEB)
2 ng Plasmid were used for amplification
Primers: VF2 and VR
Over all volume= 50 µl

PCR program (standard):

Step	Temperature [°C]	Time [s]
initial denaturation	98	120
35 cycles	98	10
	66	30
	72	30
final extension	72	300
Hold	4	ꝏ

PCR purification was performed according to manufacturers protocol (Wizard SV Gel and PCR clean-up kit, Promega)

Results:

PCR of linear pSB1C3

Investigator: MT

Aim of the experiment:

Amplification of linear pSB1C3 and introduction of restriction site: blunt at 5' and NotI at 3'

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM Forward Primer (O-038)	2,5 μl	0.5 μM
10 μM Reverse Primer (O-039)	2,5 μl	0.5 μM
Template DNA	1 µL	1 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	10 sec
	68 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Preparative digestion of P74, P165, P196, P273, P274, P275, P285 and PCR of GSY9

Investigator: Clemens

Aim of the experiment:

Procedure:

Batch for preparative digestion of P74 with XbaI and AgeI-HF

volume	reagent
2 µl	Plasmid DNA P74
3 µl	Cutsmart buffer (10x)
1 µl	XbaI
1 µl	AgeI-HF
23 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P74 with NgOMIV and AgeI-HF

volume	reagent
2 µl	Plasmid DNA P74
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	AgeI-HF
23 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P165 with PstI-HF and AgeI-HF

volume	reagent
12 µl	Plasmid DNA P165
3 µl	Cutsmart buffer (10x)
1 µl	PstI-HF
1 µl	AgeI-HF
13 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P196 with NgOMIV and PstI-HF

volume	reagent
15 µl	Plasmid DNA P196
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
10 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P273 with XbaI and HindIII-HF

volume	reagent
20 µl	Plasmid DNA P273
3 µl	Cutsmart buffer (10x)
1 µl	XbaI
1 µl	HindIII-HF
5 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P274 with AgeI-HF and PstI-HF

volume	reagent
10 µl	Plasmid DNA P274
3 µl	Cutsmart buffer (10x)
1 µl	PstI-HF
1 µl	AgeI-HF
15 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P275 with NgOMIV and PstI-HF

volume	reagent
8 µl	Plasmid DNA P275
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
17 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P285 with NgOMIV and PstI-HF

volume	reagent
12 µl	Plasmid DNA P285
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
13 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of PCR of GS9 with NgOMIV, AgeI-HF and XbaI

volume	reagent
25 µl	Plasmid DNA PCR GSY9
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	AgeI-HF
1 µl	XbaI
0 µl	ddH2O
=31 µl	TOTAL

Batch for preparative digestion of PCR of GS9 with HindIII-HF and XbaI

volume	reagent
25 µl	Plasmid DNA PCR GSY9
3 µl	Cutsmart buffer (10x)
1 µl	XbaI
1 µl	HindIII-HF
0 µl	ddH2O
=30 µl	TOTAL

Digestions were incubated at 37° over night
Samples were applied on a 1% agarose gel
Samples were seperated for 45 min at 80V

Results:

All Digests showed the expected lengths
Fragments were cut from the gel and purified according to manufacturers protocol (Wizard SV Gel and PCR clean-up system, Promega)

Transformation of P296 (pSB1C3 mGMK-Tk30, BBa_K782063) in xl1-blue

Investigator: MT

Aim of the experiment: Transformation for Poly-A-tail adding

Procedure: transformation in competent xl1-blue according to protocol + rescue

Result: plates (LB Cam) in incubator for further processing (37 °C) showed after 24 h colonies

(Re)ligations of F1013 (pSB1C3) and F1016 (phosphoryliert) + F1013 and F1005 in pSB1C3

Investigator: EF

Aim of the experiment: Ligations of PCR Produkt from GSY8 in pSB1C3 vector for later transformation and cloning

Procedure:

Ligation mixtures were prepared as following; DNA amounts were calculated using the ligation calculator http://www.insilico.uni-duesseldorf.de/Lig_Input.html :
F1013+F1016: 1.6 μL F1013, 5 μL F1016, 2μL T4-DNA-Ligase-Buffer, 1 μL T4-DNA-Ligase, 10.4 μL ddH2O
F1013+F1005: 1.6 μL F1013, 2.2 μL F1005, 2μL T4-DNA-Ligase-Buffer, 1 μL T4-DNA-Ligase, 13.2 ddH2O
Ligation was incubated for 1.5 hours at 16 °C

Thursday, Aug 25th

Phosphorylation and hybridization of O35, O36, O37

Investigator: EU

Aim of the experiment:

Phosphorylation and hybridization of O35, O36, O37

Procedure: Phosphorylation

0,5 µL Oligonucleotides
2 µL 10x T4 PNK Bufer
2 µL T4 Ligase Buffer
1 µL T4 PNK
14,5 µL H2O

incubate at 37°C for 20 min and inactivate T4PNK (for 10 min at 75°C)

Hybridization

2 µL O31
2 µL O32
in 200 µL ddH20

incubate at 95°C for 3 min, let cool down slowly

Results:

Inoculation of P296(Kill-Switch)

Investigator: EU

Aim of the experiment: production of P296

Procedure: 2x5ml LB-CAM media, each inoculated by one colony (not by rescue colonies)

Results:

Digestion of P74 + HincII

Investigator: MT

Aim of the experiment:

Digestion of P74 + HincII

Procedure:

3 µL DNA (1431 ng/µL)
1 µL HincII
14 µL ddH2O
2 µL CutSmart buffer
incubation for 2h at 37 °C

Results:'

P74 -> P1021 111,2 ng/µL

Ligation of F233+F238, F236+F234, F233+F237, F232+F240, F231+F239, F235+F241 and F248+F249

Investigator:

Aim of the experiment:

Ligation and transformation of XL1 blue

Procedure:

Batch for Ligation of F233 and F238

volume	reagent
1,7 µl	Vector F233
8,3 µl	Insert F238
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F236 and F234

volume	reagent
1,1 µl	Vector F236
8,9 µl	Insert F234
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F233 and F237

volume	reagent
3,1 µl	Vector F233
6,7 µl	Insert F237
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F232 and F240

volume	reagent
4,8 µl	Vector F232
5,2 µl	Insert F240
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F231 and F239

volume	reagent
5,6 µl	Vector F231
4,4 µl	Insert F239
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F235 and F241

volume	reagent
6,5 µl	Vector F235
3,5 µl	Insert F241
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F228 and F249

volume	reagent
2,7 µl	Vector F248
7,3 µl	Insert F249
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Ligations were performed according to SOP
XL1blue were transformed with the resulting fragments

Results:'

Cellgrowth yes/no?

Digestion of P1007 + EcoRI + SpeI

Investigator: EF

Aim of the experiment:

Digestion of P1007

Procedure:

10 µL DNA (3.6 ug)
0.25 µL EcoRI
0.25 µL SpeI
34.5 µL ddH2O
5 µL CutSmart Buffer NEB
incubation for 1h at 37 °C

Results:

Preparative digestion, gel electrophoresis and gel extraction of P288 (CMV-Promotor) and P289 (NanoLuc + Streptag + Poly-A)

Investigator: JL

Aim of experiment: Preparative digestion, gel electrophoresis and gel extraction of P288 (CMV-Promotor) and P289 (NanoLuc + Streptag + Poly-A)

Procedure:

Batches for analytical digestions:

P288: PstI and SpeI.

P29: PstI and XbaI.

volume	reagent
6 µl	Plasmid DNA
19 µl	ddH2O
3 µl	CutSmart buffer (10x)
1 µl	Each enzyme
30 µl	TOTAL

Preparative gel electrophoresis was performed at 90 V for 60 min.
Preperative gel according to SOP.
The Purification was done according to the manufacturer's protocol.

Analytical digestion and gelelectrophoresis of P293, P294, P295 (eMA pASK111)

Investigator: JL

Aim of the experiment: Analytical digestion and gelelectrophoresis of P293, P294, P295 (eMA pASK111).

Procedure:

Batch for analytical digestion for P293, P294, P295.

volume	reagent
2/1/4 µl	Plasmid DNA P293/P294/P295
2 µl	NEBuffer 4 (10x)
0.5 µl	XbaI
0.5 µl	HindIII (20 U/µl)
6/8/4 µl	ddH2O
=12 µl	TOTAL

Incubation for 120 min at 37 °C.

Analytical gelelectrophoresis was performed at 90 V for 30 min.

Results:

1 kbp ladder DNA ladder

P293

P294

500px

Friday, Aug 26

Digestion of P74 + HincII

Investigator: MT

Aim of the experiment:

Digestion of P74 + HincII

Procedure:

3 µL DNA (1431 ng/µL)
1 µL HincII
41 µL ddH2O
5 µL CutSmart buffer
* 2h; 37 °C

Results:

generuler; pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2; P74[HincII]

F1024 49.3 ng\µL

Transformation of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2

Investigator: MT

Aim of the experiment:

Amplification of Vector

Procedure:

Transformation following SOP(13.02.2013)

Digestion of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2

Investigator: MT

Aim of the experiment:

Digestion of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 + PmeI & NotI

Procedure:

7 µL DNA (77 ng/µL)
0.25 µL PmeI
0.25 µL NotI
34.5 µL ddH2O
5 µL CutSmart buffer
2h; 37 °C

Results:

generuler; pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2; P74[HincII]

F1023 7.6 ng\µL

Gelextraction PCR pSB1C3

Investigator: MT

Aim of the experiment:

Purification of PCR linear pSB1C3

Procedure:

According to Gelextraction kit; Quiagen

Results:

generuler; PCR gsy8; PCR linear pSB1C3

F1025 9.2 ng\µL

Analytical digestion of P249, P268 and P269 (each by XbaI&HindIII)

Investigator: EU

Aim of the experiment: Analyze construct for eventual preparative digestion

Procedure:

5 µl DNA (except for P249 --> 13 µl) 12µl ddH2O (except for P249 --> 4 µl) 1µl of each enzyme 2µl cut smart buffer

incubation at 37°C for 2 h Gel electrophoresis and gel extraction

Results:

In each digestion only one fragment (the vector) was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.

Preparative digestion of P272 and P273 (each by XbaI&HindIII)

Investigator: EU

Aim of the experiment: Prepare construct for ligation later on

Procedure:

5 µl DNA 36µl ddH2O 2µl of each enzyme 5µl cut smart buffer

incubation at 37°C for 2 h Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according to manufacturer’s protocol

Results:

Fragment was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.

Miniprep of P296

Investigator: EU

Aim of the experiment: Obtain plasmids

Procedure:

Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)

Plasmid was not renamed.

Results:

Concetrations in "Inventarliste"

Sequencing of P296

Investigator: EU

Aim of the experiment: Sequencing of P296

Procedure:

Sequencing batch was prepared after manufacturer's protocol:

- 7 µl of plasmid DNA (end concentration 50 - 100ng) in 8µl H2O
- 2 µl sequencing primer (one batch with VF2 and another with VR)

The different vectors we sequenced received the following barcodes:

- P296 with VF2: FR
- P296 with VR: FR

Results:

Digestion of P1007, P1008 with EcoRI HF, SpeI HF + analytical gel

Investigator: EF

Aim of the experiment: Isolation of pSB1C3 plasmid from p1007) Procedure:

p1007 digested with:

0,25 µl EcoRI (HF) 0,25 µl SpeI (HF), 5 µl CutSmart Buffer 3 µg plasmid-DNA (P1007) fill up with ddH2O (Vtotal= 50µL)

2x 25 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)

Results: Despite optimised enzyme quantity the insert seems to not have been cut out of the plasmid. One single band at 3kb --> repeat reaction; check cutting sites with genious (*)has p1007 been sequenzed before(?). However the band was extracted from the geled and freezed labeled as "8.1"

p1008 digested with:

0,25 µl EcoRI (HF) 0,25 µl SpeI (HF), 5 µl CutSmart Buffer 3 µg plasmid-DNA (P1008) fill up with ddH2O (Vtotal= 50µL)

2x 25 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)

Results: Insert was isolated by gel extraction following GelExtraction Kit instructions.

500px

Saturday, Aug 27

PCR GSY8

Investigator: MT

Aim of the experiment:

Amplification of GSY 8

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM Forward Primer (VR)	2,5 μl	0.5 μM
10 μM Reverse Primer (D20)	2,5 μl	0.5 μM
Template DNA	1 µL	10 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	10 sec
	61 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Results:

negativ two times :(

Mung Bean nuclease (MBN) digestion of F1023

Investigator: MT

Aim of the experiment:

Get rid of overhangs. Preparation of DNA for blunt ligation

Procedure:

18 µL DNA (144 ng)
2 µL MBN buffer
0.5 µL MBN
30 min; 30 °C
purification by PCR purification kit, Promega

Results:

F1026 24 ng\µL; must be wrong, because this is more than digested. Endvolume 20 µL

Dephosphorylation of F1024

Investigator: MT

Aim of the experiment:

Preparation of Vekor for blunt end Ligation

Procedure:

13 µL DNA (~50 ng\µL)
5 µL Antarctic phosphatase (AP)
2 µL AP buffer
30 min ; 37 °C
heat inactivation: 2 min; 80 °C

Results:

F1029

Ligation: F1025 +F1022 = F1027

Investigator: MT

Aim of the experiment:

Ligation: F1025 +F1022

Procedure:

1 µL F1025 (10 ng\µL)
10 µL F1022 (5 ng\µL)
2 µL buffer
1 µL T4 ligase
6 µL ddH2O
60 min; 30°C

Results:

F1025 +F1022 = F1027

Ligation: F1025 +F1026 = F1028

Investigator: MT

Aim of the experiment:

Ligation: F1025 +F1026

Procedure:

1 µL F1025 (10 ng\µL)
20 µL F1026 (24 ng\µL)
3 µL buffer
1 µL T4 ligase
4 µL ddH2O
60 min; 37 °C

Results:

F1025 +F1026 = F1028

Phosphorylation of GSY7; GSY8

Investigator: MT

Aim of the experiment:

Phosphorylation of GSY7; GSY8

Procedure:

5 µL DNA
2 µL T4 Ligase buffer
1 µL T4 PNK
12 µL ddH20
30 min; 37 °C
heat inactivation: 20 min; 65 °C

Results:

F1030 (GSY7)
F1031 (GSY8)

Over night liquid culture of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2

Investigator: MT

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Ligation: F1029 + F1030 = F1032; F1029 + F1031 = F1033

Investigator: MT

Aim of the experiment:

Ligation: F1029 + F1030 = F1032; F1029 + F1031 = F1033

Procedure:

5 µL F1029 ( ~ 30 ng) {ERROR!}
10 µL F1030/F1031 (~ 25 ng)
2 µL buffer
1 µL T4 ligase
2 µL ddH2O
60 min; 37 °C

Results:

F1029 + F1030 = F1032
F1029 + F1031 = F1033
Both negativ, due to miscalculation

Transformation of F1027; F1028; F1032; F1033

Investigator: MT

Aim of the experiment:

Amplification of Vector

Procedure:

Transformation following SOP(13.02.2013)

Sunday, Aug 28

PCR GSY8

Investigator: MT

Aim of the experiment:

Amplification of GSY 8

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM Forward Primer (D20)	2,5 μl	0.5 μM
10 μM Reverse Primer (VR)	2,5 μl	0.5 μM
Template DNA	1 µL	10 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	10 sec
	58 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Results:

Over night liquid culture of F1032; F1028

Investigator: MT

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Plasmidpreparation of liquid culture of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2

Investigator: MP

Aim of the experiment:

Purification of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2

Procedure:

According to Mini-prep. kit, SLG

Results:'

P1009 608.6 ng/µL

Week 16, Aug 29nd - Sep 4th

Monday, Aug 29nd

Plasmid preparation of liquid culture of F1032(clon 1); F1032(clon 2)

Investigator: JL

Aim of the experiment:

Purification of F1032(clon 1); F1032(clon 2)

Procedure:

According to Mini-prep. kit, Quiagen

Results:

P 1010 448.4 ng/µL
P 1011 344.6 ng/µL

Analytical digestion of P1010; P1011

Investigator: JL

Aim of the experiment:

verify constructs: P1010; P1011

Procedure:

2 µL DNA
0.5 µL EcoRI
0.5 µL PstI
1 µL CutSmart buffer
6 µL ddH20

Results:

1kb ladder; P1010; P1011

PCR and purification of GSY7_new and GSY8

Investigator: EU

Aim of the experiment:

Amplification of GSY 7_new and GSY 8

Procedure:

Same procedure for both GSYs:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM Forward Primer (VR)	2,5 μl	0.5 μM
10 μM Reverse Primer (D20)	2,5 μl	0.5 μM
Template DNA	1 µL	10 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	10 sec
	98 °C	30 sec
	61 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Purification according to Promega PCR purification kit

Results: GSY7: 9,4 ng/µl GSY8: 1,5 ng/µl, probably contaminated with GSY7_new

Phosphorylation of GSY7_new and GSY8

Investigator: EU

Aim of the experiment:

Phosphorylation of GSY7_new; GSY8

Procedure:

5 µL DNA
2 µL T4 Ligase buffer
1 µL T4 PNK
12 µL ddH20
30 min; 37 °C
heat inactivation: 10 min; 75 °C

Results:

F1034 (GSY7_new)
F1035 (GSY8)

Ligation: F1034 + F1029 = F1036; F1035 + F1029 = F1037

Investigator: EU

Aim of the experiment:

Ligation: F1034 + F1029 = F1036; F1035 + F1029 = F1037

Procedure:

5 µL F1029 ( ~ 10 ng)
10 µL F1034/F1035 (~ 25 ng)
2 µL buffer
1 µL T4 ligase
2 µL ddH2O
60 min; 37 °C

Results:

F1029 + F1034 = F1036
F1029 + F1035 = F1037

Preparative digestion of P297, P299, P279, P285, P285, P277, P312 & P251

Investigator: Clemens

Aim of the experiment:

Preparation for cloning in pSB1C3/pASK111

Procedure:

* Batch for preparative digestion of P297 with AgeI-HF & PstI-HF

volume	reagent
5 µl	Plasmid DNA P297
3 µl	Cutsmart buffer (10x)
1 µl	AgeI HF
1 µl	PstI-HF
220 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P299 with NgOMIV and PstI-HF

volume	reagent
6 µl	Plasmid DNA P299
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
19 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P279 with NgOMIV & PstI-HF

volume	reagent
20 µl	Plasmid DNA P279
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
5 µl	ddH2O
=30 µl	TOTAL

* Batch for preparative digestion of P285 with AgeI-HF & PstI-HF

volume	reagent
15 µl	Plasmid DNA P297
3 µl	Cutsmart buffer (10x)
1 µl	AgeI HF
1 µl	PstI-HF
10 µl	ddH2O
=30 µl	TOTAL

* Batch for preparative digestion of P277 with AgeI-HF & PstI-HF

volume	reagent
6 µl	Plasmid DNA P277
3 µl	Cutsmart buffer (10x)
1 µl	AgeI HF
1 µl	PstI-HF
19 µl	ddH2O
=30 µl	TOTAL

* Batch for preparative digestion of P312 with AgeI-HF & PstI-HF

volume	reagent
5 µl	Plasmid DNA P312
3 µl	Cutsmart buffer (10x)
1 µl	AgeI HF
1 µl	PstI-HF
20 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P251 with NgOMIV & PstI-HF

volume	reagent
15 µl	Plasmid DNA P251
3 µl	Cutsmart buffer (10x)
1 µl	NgOMIV
1 µl	PstI-HF
10 µl	ddH2O
=30 µl	TOTAL

Digestions were incubated for 3h at 37°C
Fragments were cut from the gel and purified by gelectraction (promega)

Results:

Fragments were renamed (see Inventarliste) and concentrations were measured

Ligation of F254+ F255, F256+F257, F256+F258 & F260+F312

Investigator: Clemens

Aim of the experiment:

Ligation

Procedure:

Batch for Ligation of F254 and F255

volume	reagent
3 µl	Vector F254
7 µl	Insert F255
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F257 and F256

volume	reagent
1.9 µl	Vector F257
8.1 µl	Insert F256
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F258 and F256

volume	reagent
1.3 µl	Vector F258
8.7 µl	Insert F256
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Batch for Ligation of F312 and F260

volume	reagent
1.2 µl	Vector F312
8.8 µl	Insert F260
2 µl	10X DNA-Ligase-buffer
1 µl	T4-Ligase
7 µl	H₂O
=20 µl	TOTAL

Ligations were performed according to SOP

Analytical digestion and gelelectrophoresis of pASK111, P268 (SUMO-PAS), P6, and P259 (both SA)

Investigator: Niklas

Aim of the experiment: verification before cloning for fermentation

Procedure:

volume	P268/ P259/ P6/ pASK111
5,8 µl/ 17 µl/ 8,33 µl/ 14,2 µl	Plasmid DNA
2 µl	cut smart (10x)
0.5 µl	XbaI
0.5 µl	HindIII
11,2 µl/ 0 µl/ 8,67 µl/ 2,8 µl	ddH2O
=20 µl	TOTAL

Incubation for 90 min at 37 °C.

Analytical gelelectrophoresis was performed at 90 V for 60 min.

Results:

on of the enzymes was contaminated

Transformation of P310 in BL 21; P6, P259, P268, pASK111, F1034+F1028 in xl1-blue

Investigator: NA

Procedure:

CaCl₂-competent E. coli cells were taken from the stock in –80 °C freezer and gently thawed on ice

1 µl (retrafo)/ 7 µl (ligation) of DNA was added to 50 µl of competent cells and gently mixed

30 min incubation on ice

5 min heat shock at 37 °C

Added 0,9 ml LB medium to each tube

Incubation for 60 min at 37 °C in the 180 rpm cell-culture shaker

50 µl of the cell suspension was plated on one plate

The rest were centrifuged for 1 min at 13,000 rpm and the supernatant was dicarded

The pellet was resuspended in 50 µl of LB-medium and this concentrated cell suspension was plated on a plate.

Tuesday, Aug 30rd

PCR on GSY7 and GSY8

Investigator: CG

Aim of the experiment:

Amplification of GSY 7 and GSY 8

Procedure:

Same procedure for both GSYs:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM Forward Primer (VR)	1,5 μl	0.25 μM
10 μM Reverse Primer (D20)	1,5 μl	0.25 μM
Template DNA	2 µL	10 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
45 cycles	98 °C	10 sec
	98 °C	30 sec
	60 °C	90 sec
Final extension	72 °C	120 sec
Hold	4 °C

Results:

GSY8 negative: smear at the upper end of the gel.

Preparative digestion of P270 & P308

Investigator: Clemens

Aim of the experiment:

Preparation for cloning in pSB1C3

Procedure:

Batch for preparative digestion of P270 with EcoRI-HF & Spe-HF

volume	reagent
25 µl	Plasmid DNA P270
3 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF
1 µl	SpeI-HF
0 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P308 with EcoRI-HF and XbaI

volume	reagent
10 µl	Plasmid DNA P308
3 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF
1 µl	XbaI
15 µl	ddH2O
=30 µl	TOTAL

Digestions were incubated for 3h at 37°C
Fragments were cut from the gel and purified by gelectraction (promega)

Results:

Fragments were renamed (see Inventarliste) and concentrations were measured

Cloning of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) in pSB1C3

Investigator: CG

Aim of the experiment:

Cloning of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) in pSB1C3

Procedure:

17 µl pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) digestion with 1 µl Mung Bean Nuclease and 2 µl buffer for 30 min. at 30°C to receive blunt ends
Ligation of 8.7 µl pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) and 1.3 µl pSB1C3
Overnight incubation at 16 °C

Retransformation of P258

Investigator: CG

Aim of the experiment:

Amplification of Vector

Procedure:

Transformation following SOP(13.02.2013)

Digestion of P1005, P1006, P1007 with XbaI, PstI HF + analytical gel

Investigator: EF

Aim of the experiment: Isolation of insert for further construction of hypoxia system Procedure:

p1005, p1006, p1007 digested with:

0,25 µl EcoRI (HF) 0,25 µl SpeI (HF), 5 µl CutSmart Buffer 3 µg plasmid-DNA (Pp1005, p1006, p1007) fill up with ddH2O (Vtotal= 50µL)

30 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)

Digestions were incubated for 1h at 37°C

Results: Insert and vector were clearly separated. All cut vector remained at the expected position of 2kb. Inserts were isolated following extraction kit protocol . F number and concentrations were included into the Inventarliste. Remain of 30µl (with dye) frozen at -20 C -> Labeled as 5.1; 6,1; 7.2

Digestion of P1007 with EcoRI HF, SpeI HF + analytical gel

Investigator: EF

Aim of the experiment: Isolation of vector. Verification of digestion performed on 29th, Friday Procedure:

p1007 digested with:

0,25 µl EcoRI (HF) 0,25 µl SpeI (HF), 5 µl CutSmart Buffer 3 µg plasmid-DNA (p1007) fill up with ddH2O (Vtotal= 50µL)

Digestion was incubated for 1h at 37°C

30 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)

Results: Again plasmid wasn´t cut. One single band at 3kb. Further procedur: sequence plasmid (?) repeat ligation to generate p1007. Isolate pSB1C3 from another plasmid.

[File to be uploaded]

Ligation of F1001 and F1002

Investigator: EF

Aim of the experiment: generate p1007 due to gel results (since 28th, Thursday) Procedure: Ligation was performed as follows: 6,3 µl F1001, 5,3 µl F1002, 2 µl T4-DNA-Ligase Buffer, 1 µl T4-DNA-Ligase, filled up with ddH20 to 20 µl *3:1 vector-insert ratio

Ligation of F248 and 1015

Investigator: EF 'Aim of the experiment: hypoxia Procedure: Ligation was performed as follows: 1 µl F248, 5 µl F1015, 2 µl T4-DNA-Ligase Buffer, 1 µl T4-DNA-Ligase, filled up with ddH20 to 20 µl *Approximate 3:1 vector insert ratio

Results: Plates incubating over night at 37C

Sequencing of P259 (SA from GSY6; P303 and P304 (eMA)

Investigator: NA

Procedure:

Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer) - all samples: VF2
barcodes in stock list

Picking of of E. coli XL1 blue with P6, pASK111, P268

Investigator: NA

Procedure:

2 colonies were picked.

These tubes were transferred in a cell culture shaker at 37 °C and were incubated overnight

Inocculation of preculture (P310 eMA-HisTag)

Investigator: NA

Procedure:

2 colonies were picked (20 mL LB with Cam)

the preculture was transferred in a cell culture shaker at 37 °C and were incubated overnight

harvesting SUMO Protease

Investigator: NA

Aim of the experiment: SUMO Protease production

Procedure:

6 x 2 L cultures
centrifuge cultures for 30 min at 6000 rpm
freeze pellet (120.5 g)

Wednesday, Aug 31st

Over night liquid cultures of P1007 and P1012

Investigator: EF

Aim of the experiment:

Obtaining enough cellmass for plasmid preparation. Liquid cultures of Turbo and XL1 blue cells.

Procedure:

Inoculation of 5 mL LB-medium with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Phosphorylation of F1036

Investigator: MT

Aim of the experiment:

Phosphorylation of F1036

Procedure:

36 µL DNA (*350 ng)
4 µL T4 ligase buffer
1 µL PNK
30 min; 37 °C
heat deactivation: 20 min; 65 °C

Ligation: F1029 + F1037 = F1038

Investigator: MT

Aim of the experiment:

Ligation: F1029 + F1037 = F1038

Procedure:

0.5 µL F1029 (30 ng\µL)
10 µL F1037 (9 ng\µL)
2 µL T4 ligase buffer
1 µL T4 ligase
7 µL ddH2O
over night ; 16 °C

Results:

F1029 + F1037 = F1038

Miniprep of various plasmids, analytical digestion, sequencing

Investigator: CG

Aim of the experiment: Obtain plasmids for: eMA, PAS-Lys-Sumo, pASK111, Streptavidin (non-codon-optimized)

Procedure:

Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)
Digestion of about 250 ng for each eMA plasmid with EcoRI and PstI

Results:

Names and concetrations in "Inventarliste"
Sequencing results
Gel:

1. GSY8, 2. - 5.: P319-P322 with EcoRI / PstI

Cloning of Streptavidin (non-codon-optimized) into pASK111

Investigator: JL, NA, CG

Aim of the experiment: Obtain Streptavidin (non-codon-optimized) in expression vector

Procedure:

Preparative digestion of 42 µl P6 (Streptavidin) and 42 µl P315, 5 µl CutSmart and 1.5 µl XbaI/HindIII
Gel extraction
Ligation: 5.9 µl pASK111 + 4.1 µl SA + 2 µl ligase buffer + 7 µl ddH2o + 1 µl T4 ligase
Transformation according to SOP

Results:

Gel:

1. Streptavidin (non-codon-optimized), 2. pASK111

Preparative digestion of P296 and P73

Investigator: EU

Aim of the experiment: Prepare construct for ligation later on

Procedure:

5 µl DNA 36µl ddH2O 2µl of each enzyme (P296 --> EcoRI&SpeI, P73 --> EcoRI&XbaI) 5µl cut smart buffer

incubation at 37°C for 3 h Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according to manufacturer’s protocol

Results:

Fragments were expected at about 1 kb (P296) and 2,5 kb (P73). This could be shown comparing with 1kb DNA ladder.

Ligation: F269 + F270 = F271

Investigator: EU

Aim of the experiment:

Ligation: F269 + F270 = F271

Procedure:

5 µL F269 ( ~ ng)
10 µL F270 (~ ng)
2 µL buffer
1 µL T4 ligase
2 µL ddH2O
ONT; 16 °C

Results:

F269 + F270 = F271

PCR and purification of GSY7_new and GSY8

Investigator: CG, EU

Aim of the experiment:

Amplification of GSY 7_new and GSY 8

Procedure:

Same procedure for both GSYs:

PCR using PfuUltra II Fusion HotStart DNA Polymerase according to manufacturer’s online protocol

Component	10 µL reaction	Final concentration
PfuUltra II Hotstart PCR Master Mix	25 µL	1 X
10 μM Forward Primer (O-038)	2,5 μl	0.5 μM
10 μM Reverse Primer (O-039)	2,5 μl	0.5 μM
Template DNA	1 µL	10 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	2 min
40 cycles	98 °C	10 sec
	98 °C	20 sec
	45-64,7 °C (gradient)	20 sec
Final extension	72 °C	30 sec
Hold	4 °C

Purification according to Promega PCR purification kit

Results: no amplification recognizable

harvesting SUMO Protease

Investigator: NA

Aim of the experiment: SUMO Protease production

Procedure:

resuspend pellet in PBS + 10 mM EDTA
homogenize cells with PANDA
centrifuge cultures for 30 min at 8000 rpm (protein in supernantant)
dialysis against IMAC buffer

Inocculation and induction of eMA-HisTag (P310)

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

2 L LB shaking flask

the cell culture was incubated at 37 °C
induction with 200 µl anhydro tetracycliine (2mg/ml) at OD= 0,55
production over night

Thursday, Sep 1st

Miniprep of F261, F262, F263, F264, I739001, P305 & P258 ,analytical digestion and sequencing

Investigator: Clemens

Aim of the experiment: Confirm sucessful cloning

Procedure:

Miniprep was performed according to manufacturer's protocol (QIAprep, Qiagen)
Analytic digestion was performed to check if the cloning was successful

Batch for analytical digestion of P323/P324 with PstI-HF and EcoRI-HF

volume	reagent
1 µl/ 0.5 µl	Plasmid DNA P323/P324
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P325/P326 with PstI-HF and EcoRI-HF

volume	reagent
1 µl/ 0.5 µl	Plasmid DNA P326/P325
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P327/P328 with PstI-HF and EcoRI-HF

volume	reagent
1 µl/ 0.5 µl	Plasmid DNA P328/P327
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P329/P330 with PstI-HF and EcoRI-HF

volume	reagent
0.5 µl/ 0.5 µl	Plasmid DNA P329/P330
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7.5 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P331/P332 with PstI-HF and EcoRI-HF

volume	reagent
0.5 µl/ 0.5 µl	Plasmid DNA P331/P332
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7.5 µl	ddH2O
=10 µl	TOTAL

Batch for analytical digestion of P333/P334/P322 with AgeI-HF and EcoRI-HF

volume	reagent
0.5 µl/ 0.5 µl/ 0.5 µl	Plasmid DNA P333/P334/P322
1 µl	Cutsmart buffer (10x)
0.5 µl	EcoRI-HF (10 U/µl)
0.5 µl	PstI-HF (20 U/µl)
7.5 µl/ 7.5 µl/ 7.5 µl	ddH2O
=10 µl	TOTAL

Digestions were incubated for 1.5h at 37°C
Samples were run on an 1% agarose gel for 45 min at 90V

Results:

Except for P329, P330 and P322 all fragments were of the expected size
Cloning of the inserts of P29 and P30 was started again.

For confirmation of the Sequence the following plasmids were send for sequencing:

P323 (VF2 & VR)
P331 (VF2)
P333 (VF2)
P328 (VF2)
P326 (VF2)

Preparative digestion of P333, P308, P331 and P301

Investigator: Clemens

Aim of the experiment:

Cloning of new constructs

Procedure:

Batch for preparative digestion of P333 with NgOMIV and PstI-HF

volume	reagent
6 µl	Plasmid DNA P333
3 µl	Cutsmart buffer (10x)
1 µl	PstI-HF
1 µl	NgOMIV
19 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P333 with AgeI-HF and PstI-HF

volume	reagent
6 µl	Plasmid DNA P333
3 µl	Cutsmart buffer (10x)
1 µl	PstI-HF
1 µl	AgeI-HF
19 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P308 with XbaI and EcoRI-HF

volume	reagent
15 µl	Plasmid DNA P308
3 µl	Cutsmart buffer (10x)
1 µl	XbaI
1 µl	EcoRI-HF
10 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P333 with SpeI-HF and EcoRI-HF

volume	reagent
8 µl	Plasmid DNA P331
3 µl	Cutsmart buffer (10x)
1 µl	EcoRI-HF
1 µl	SpeI-HF
17 µl	ddH2O
=30 µl	TOTAL

Batch for preparative digestion of P301 with PstI-HF and NgOMIV

volume	reagent
6 µl	Plasmid DNA P301
3 µl	Cutsmart buffer (10x)
1 µl	PstI-HF
1 µl	NgOMIV
19 µl	ddH2O
=30 µl	TOTAL

Digestions were incubated for 3h at 37°C
Samples were applied on a 1% agarose gel and run at 90V for 45min

Results:

Digestions of P308, P331 and P301 showed the expected fragment sizes.
These fragments were cut from the gel and purified by gelextraction (Promega)
Samples were renamed and given Fragmentnumbers

The Digestions of P333 showed fragments of unexpected length. The Ligation of eMA in pSB1C3 (previous step) failed. This ligation has to be repeated.

PCR and purification of GSY7_new and GSY8

Investigator: MP, EU

Aim of the experiment:

Amplification of GSY 7_new and GSY 8

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
each GSY was amplified two times; once with Q5 GC-Enhancer and once without

Component	25 µL reaction	Final concentration
5X Q5 Reaction Buffer	5 µL	1 X
10 mM dNTPs	0.5 µL	200 μM
10 μM Forward Primer (D20)	1.25 μl	0.5 μM
10 μM Reverse Primer (VR)	1.25 μl	0.5 μM
Template DNA	1 µL	10 ng
Q5 High-Fidelity DNA Polymerase	0.25 μl	0.02 U/μl
Nuclease-Free Water	to 25 μl (minus 5µl for GC-Enhancer respectively)

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	5 - 10 sec
	61 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	16 °C

Note: Use of the NEB T m Calculator is highly recommended.

Purification according to Promega PCR purification kit

Results: no amplification GSY8 recognizable, GSY7did work

Transformation of F271

Investigator: EU

Aim of the experiment:

Transformation of F271 for further application

Procedure:

3 µL DNA were added to blr cells
incubation on ice for 20 min
heatshock in 42°C for 40s
incubation on ice for 4 min
700µl LB-medium were added
incubation for 1h in 37°C shaker
centrifugation for 3 min

Results:

Transformation of F1038

Investigator: EU

Aim of the experiment:

Transformation of F1038 for further application

Procedure:

3 µL DNA were added to blr cells
incubation on ice for 20 min
heatshock in 42°C for 40s
incubation on ice for 4 min
700µl LB-medium were added
incubation for 1h in 37°C shaker
centrifugation for 3 min

Results:

harvesting of eMA-HisTag

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

centrifugate at 6000 rpm for 30 min (OD= 6.15)
11,1 g pellet
SDS-PAGE after protocol
resuspend pellet in 20 mM Tris/HCl + 50 mM NaCl
homogenize cells with PANDA
centrifuge 30 min at 18000 rpm
denaturate inclusion bodies in 16 ml Gnd-Chl (pH 1.5) over night

results:

marker, eMA before induction, eMA after induction, ULP after induction (SUMO protease)

Friday, Sep 2nd

Ligation of F274+F275, F276+F260 and F279+F240

Investigator: Clemens

Aim of the experiment:

Cloning of new constructs

Procedure:

Results:

harvesting of eMA-HisTag

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

add 4 ml Gnd-Chl because pellet did not dissolve over night, continue shaking for few hours
centrifugate for 15 min at 15000 rpm (protein in supernatant)
refolding in 1.5 L cold PBS over night

purification of SUMO protease using ÄKTA purifier

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

centrifugation
destroying DNA using ultrasonic for 10 min
sterilfiltration
purification due to HisTag affinity of protein to nickel in column (buffer: 20 mM Tris/HCl + 500 mM NaCl
over night

Procedure:

purification stopped because of pressure alarm, was restarted an showed no SUMO protease in the sample

Cloning of extended MCS into pDSG and pcDNA5 vector

Investigator: CG

Aim of the experiment: Extending the MCS of pDSG and pcDNA5 for cloning of BioBricks

Procedure:

Digestion of 5 µl P291 (pDSG) and 15 µl P339 (pcDNA) with SphI and NruI-HF for pDSG and MluI-HF for pcDNA5
Gelextraction of both signals at about 4 kb
Oligo-hybridzation of O35/O36 and O36/O37 wo prior phosphorylation to obtain a total concentration of 17 ng/µl
Ligation of oligo-hybridzation and vector-fragements according to calculations in the Inventarliste and overnight incubation at 16°C

Procedure:

expected signals after digestion: pDSG with 4 kb and 1.7 kb (lane 1), pcDNA with 4 kb and 1 kb (lane 2)

Miniprep of 2x pcDNA5 vector and 2x Streptavidin (nco) in pASK111

Investigator: CG

Aim of the experiment: Obtain plasmids for pcDNA5 vector and 2x Streptavidin (nco) in pASK111

Procedure:

Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)

Saturday, Sep 3nd

Transformation of F285; F286

Investigator: MT

Aim of the experiment:

Amplification of F285; F286

Procedure:

Transformation following SOP(13.02.2013)

Digestion of P1009 + PmeI&NotI

Investigator: MT

Aim of the experiment:

Digestion of P1009 + PmeI&NotI

Procedure:

33 µL DNA (~600 ng/µL)
2 µL PmeI
1 µL NotI
9 µL ddH2O
5 µL CutSmart buffer
incubation for 1h at 37 °C

Results:

F1039 80 ng/µL

Sunday, Sep 4th

Phosphorylation of F1040 (PCR product GSY7)

Investigator: MT

Aim of the experiment:

Phosphorylation of F1040 (PCR product GSY7)

Procedure:

15 µL F1040 (20 ng/µL)
5 µL T4 Ligase buffer
1 µL T4 PNK
29 µL ddH20
30 min; 37 °C
heat inactivation: 20 min; 65 °C

Results:

F1041 (PCR product GSY7)

Mung Bean nuclease (MBN) digestion of F1039 (pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 [PmeI+NotI])

Investigator: MT

Aim of the experiment:

Get rid of overhangs. Preparation of DNA for blunt ligation

Procedure:

18 µL F1039 ( 80 ng/µL)
2 µL 10x CutSmart buffer
0.25 µL MBN (10 u/µL)
60 min; 30 °C
purification by PCR purification kit, Promega

Results:

F1042 30 ng\µL

Ligation: F1042 +F1025 = F1043

Investigator: MT

Aim of the experiment:

Ligation: F1042 +F1025

Procedure:

5.5 µL F1025 (9.2 ng\µL)
8.2 µL F1042 (35 ng\µL)
2 µL buffer
1 µL T4 ligase
3.5 µL ddH2O
over night; 16 °C

Results:

F1042 +F1025 = F1043

Ligation: F1041 +F1029 = F1044

Investigator: MT

Aim of the experiment:

Ligation: F1041 +F1029

Procedure:

1.6 µL F1029 (30 ng\µL)
23 µL F1041 (6 ng\µL)
3 µL buffer
1 µL T4 ligase
1.3 µL ddH2O
over night; 16 °C

Results:

F1041 +F1029 = F1044

Cloning of SUMO-PAS in pASK75

Investigator: JL, EF

Aim of the experiment: Ligation of F158 and "P310" (JL) (SUMO+PAS-Lysin in pASK75):

5,6 µL
2,4 µL
2 µL
1 µL T4-DNA-Ligase
fill up with ddH2O to 20 µL

Transformation in NEB Turbo cells of 10 µL ligation

Week 17, Sep 5th - Sep 11th

Monday, Sep 5th

harvesting of eMA-HisTag

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

centrifugate after refolding at 11500 rpm for 30 min

results:

marker, eMA before induction, after induction, after denaturation and refolding

Inocculation of P341 (E.coli Bl-21; 50 ml LB) in M9 medium for fermentation

Investigator: NA

Procedure:

M9 medium with Cam (1:1000) was inocculated with preculture (~50 mL) of P258 (pASK111+Streptavidin)

the culture was incubated in the shaker over night at 37°C

results:

a 50 ml culture with Ecoli Bl21 was induced

the SDS PAGE shows no streptavidin expression after induction

next fermentation in pSA (not pASK111)

Tuesday, Sep 6th

Phosphorylation of F1005, F1016

Investigator: EF

Aim of the experiment: to be completed

Ligation of F1045, F1046

Investigator: EF

Aim of the experiment: to be completed

Ligation of F1005, F10016 (GelEx GSY8) in F1013

Wednesday, Sep 7th

harvesting of eMA-HisTag

Investigator: NA

Aim of the experiment: eMA-HisTag production

Procedure:

precipitation with ammonium sulfate gradient (10% to 90%)
the percentage was increased in 10% steps, after each addition of ammonium sulfate the solution was centrifugated at 8500 rpm for 20 min
SDS-PAGE: samples of the supernatants

results:

The pellets of the precipitations with 50%, 60% and 70% were pooled and dialysed against IMAC buffer Next step: Äkta

MidiPrep of pSB1C3 with RFP generator (P4)

Investigator: NA

Aim of the experiment: purification of CMV Nanoluc StrepTag PolyA (P312)

Procedure: MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)

Results:

3268 ng/µl in 80 µl

Inocculation of fermenter

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

inocculation with 50 ml preculture (P20 in LB medium)
pO₂= 60 %; Temp= 37°C, pH~7
growth over night
OD next morning: 0.4

Thursday, Sep 8th

Fermentation

Investigator: NA

Aim of the experiment: Streptavidin production

Procedure:

exponential feed (Amp) for ~13 h (about 3-4 L); start at OD= 7.5 (glucose test negative)
Induction of streptavidin expression (IPTG) at OD= 30
production over night

Friday, Sep 9th

harvesting streptavidin

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

OD= 41.4
centrifuge culture for 1 h at 4800 rpm
resuspend pellet (275 g)in 20mM Tris HCl + 500 mM NaCl(pH 8)
homogenize with PANDA
the resulting lysate was transferred into centrifuge tubes and spun down (4°C, 9000 rpm, 30 mins). The supernatant was cast away and the pellet was resuspended in 6M Gua-HCl (pH = 1.5) at 4°C overnight.

Saturday, Sep 10th

Sunday, Sep 11th

harvesting streptavidin

Investigator: NA

Aim of the experiment: streptavidin production

Procedure:

the denaturated protein solution was refolded in 15 L 1x PBS (added drop wise) over night
the solution was centrifugated at 9500 rpm for 20 minutes, the pellet was stored in the freezer, the supernatant will be concentrated via cross flow and precipitated with ammonium sulfate afterwards

results:

Week 18, Sep 12th - Sep 18th

Tuesday, Sep 13th

Digestion of P74

Investigator: MT

Aim of the experiment:

Digestion of P74

Procedure:

F1055:

2 µL DNA (1431 ng/µL)
2 µL CutSmart buffer
0.25 µL HincII (10 u/µL)
16 µL ddH2O
incubation for 1h at 37 °C

F1056:

2 µL DNA (1431 ng/µL)
2 µL CutSmart buffer
0.25 µL HincII (10 u/µL)
0.25 µL AgeI (20 u/µL)
15.5 µL ddH2O
incubation for 1h at 37 °C

F1057:

2 µL DNA (1431 ng/µL)
2 µL CutSmart buffer
0.25 µL HincII (10 u/µL)
0.25 µL NgoMIV
15.5 µL ddH2O
incubation for 1h at 37 °C

Results:

1Kb ruler, F1055[HincII], F105[HincII&AgeI]6, F1057[HincII&NgoMIV], P1017[EcoRI&SpeI]

F1055 49.5 ng/µL
F1056 37.0 ng/µL
F1057 29.7 ng/µL

Analytical digestion of P1017

Investigator: MT

Aim of the experiment:

Analytical digestion of P1017

Procedure:

2 µL DNA (312 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL EcoRI
15.5 µL ddH2O
incubation for 1h at 37 °C

Results:

1Kb ruler, F1055[HincII], F105[HincII&AgeI]6, F1057[HincII&NgoMIV], P1017[EcoRI&SpeI]

PCR of GSY10

Investigator: MT

Aim of the experiment:

Amplification of GSY10

Procedure:

PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol

Component	50 µL reaction	Final concentration
Q5® High-Fidelity 2X Master Mix	25 µL	1 X
10 μM VR	2,5 μl	0.5 μM
10 μM VF2	2,5 μl	0.5 μM
Template DNA	0.1 µL	1 ng
Nuclease-Free Water	to 50 μl

Thermocycling Conditions for a Routine PCR:

STEP	TEMP	TIME
Initial Denaturation	98 °C	30 sec
35 cycles	98 °C	10 sec
	62 °C	30 sec
	72 °C	60 sec
Final extension	72 °C	120 sec
Hold	4 °C

Dephosphorylation of F1055

Investigator: MT

Aim of the experiment:

Preparation of Vekor for blunt end Ligation

Procedure:

15 µL F1055 (~50 ng\µL)
1 µL FastAP (1 u/µL)
2 µL 10x FastAP buffer
10 min ; 37 °C
heat inactivation: 5 min; 75 °C

Results:

F348

Digestion of P1017

Investigator: MT

Aim of the experiment:

Digestion of P1017

Procedure:

10 µL DNA (312 ng/µL)
5 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
34.5 µL ddH2O
incubation for 1h at 37 °C

Results:

1Kb ruler, P1017[SpeI&PstI], P1017[SpeI&PstI], F362: PCR-GSY7[AgeI], PCR-GSY7, PCR-GSY8

F350

Over night liquid culture of P1009

Investigator: MT

Aim of the experiment:

Getting enough cellmass for plasmid preparation

Procedure:

Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
Incubate over night at 37 °C in shaker

Wednesday, Sep 14th

Gelextraction of F357[NgoMIV]; P1006[XbaI&PstI]

Investigator: MT

Aim of the experiment:

Gelextaction of F357[NgoMIV]; P1006[XbaI&PstI]

Procedure:

Using gelextraction kit, Promega

Results:

1kb ladder, F357[NgoMIV]; P1006[XbaI&PstI]

F357[NgoMIV] -> F364 41 ng/µL
P1006[XbaI&PstI] -> F365 9.1 ng/µL

Ligation: F1057 + F364 = F366

Investigator: MT

Aim of the experiment:

Ligation: F1057 + F364

Procedure:

1,6 µL F1057 (29.7 ng\µL)
2.1 µL F364 (41 ng\µL)
3 µL buffer
1 µL T4 ligase
22.3 µL ddH2O
30 min; RT

Results:

F1057 + F364 = F366

Ligation: F350 + F365 = F367

Investigator: MT

Aim of the experiment:

Ligation: F350 + F365

Procedure:

2,6 µL F350 (19 ng\µL)
2.1 µL F365 (9.1 ng\µL)
3 µL buffer
1 µL T4 ligase
15.4 µL ddH2O
30 min; RT

Results:

F350 + F365 = F367

Digestion of P1008

Investigator: MT

Aim of the experiment:

Digestion of P1008

Procedure:

10 µL P1008 (256.5 ng/µL)
5 µL CutSmart buffer
0.25 µL XbaI
0.25 µL PstI
34.5 µL ddH2O
incubation for 1h at 37 °C

Results:

1Kb ruler, ... P1008[XbaI&PstI]

P1008 -> F368 ~1 ng/µL

Maybe do it again, fragments do not have the right size, apparently.

Transformation of F366; F367

Investigator: MT

Aim of the experiment:

Amplification of Vector

Procedure:

Transformation following SOP(13.02.2013)

Analytical digestion of P296 and F269

Investigator: EU

Aim of the experiment: Analyze construct for eventual preparative digestion

Procedure:

2 µl DNA 15µl ddH2O 1µl of PstI 2µl cut smart buffer

incubation at 37°C over night Gel electrophoresis and gel extraction

Results:

Preparative digestion of P313, P296 and P73

Investigator: EU

Aim of the experiment: Prepare construct for ligation later on

Procedure:

10 µl (P73)/ 15 µl (P296)/ 20 µl (P313) DNA 2µl of each enzyme (P296&P313 --> EcoRI&SpeI, P73 --> EcoRI&XbaI) 5µl cut smart buffer ad 50 µl ddH2O

incubation at 37°C over night Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according to manufacturer’s protocol

Results:

P296 [EcoRI&SpeI] --> F378
P313 [EcoRI&SpeI] --> F383
P73 [EcoRI&XbaI] --> F379

Ligation: F269 + F270 = F380; F269 + F92 = F381; F269 + F133 = F382

Investigator: EU

Aim of the experiment:

Ligation:

- F269 + F270 = F380
- F269 + F92 = F381
- F269 + F133 = F382

Procedure:

3 µL F269 (6,3 ng)
0,5 µL F270 (5,6ng)/ 0,25 µl F92 (6,75 ng)/ 0,25 µl F133 (13 ng)
0,5 µL buffer
0,5 µL T4 ligase
0,5/0,75 µL ddH2O
ONT; 16 °C

Results:

F269 + F270 = F380
F269 + F92 = F381
F269 + F133 = F382

Sequencing of P313

Investigator: EU

Aim of the experiment: Sequencing of P313

Procedure:

Sequencing batch was prepared after manufacturer's protocol:

- 6 µl of plasmid DNA (end concentration 58,6 ng) in 9µl H2O
- 2 µl sequencing primer (VF2)

The different vectors we sequenced received the following barcodes:

- P313 with VF2: FR12904387

Results:

Thursday, Sep 15th

Digestion of P1008

Investigator: MT

Aim of the experiment:

Digestion of P1008

Procedure:

10 µL P1008 (256.5 ng/µL)
5 µL CutSmart buffer
0.25 µL XbaI
0.25 µL PstI
34.5 µL ddH2O
incubation for over night at 37 °C

Results:

P1008[XbaI&PstI], P1008[XbaI&PstI], 1Kb ruler

P1008[XbaI&PstI] -> F375 32 ng/µL

Ligation: F63 + F375 = F377

Investigator: MT

Aim of the experiment:

Ligation: F63 + F375

Procedure:

2.2 µL F63 (45 ng\µL)
6.3 µL F375 (32 ng\µL)
3 µL buffer
1 µL T4 ligase
17.5 µL ddH2O
30 min; RT

Results:

F63 + F375 = F377

Fill in of overhangs of F386 with Large Klenow fragment

Investigator: MT

Aim of the experiment:

3' overhang removal and fill-in of 3' recessed (5' overhang) ends using DNA Polymerase I, Large (Klenow) Fragment
short: create blunt ends, needed for ligation

Procedure:

17.09 µL F386 (25.9 µL)
0.66 µL 10 mM dNTP Mix
2 µL T4 Ligase buffer
0.25 µL Klenow Fragment
15 min; RT
heat inactivation: 20 min; 75 °C

Results:

F387

Incubation of F386 with Q5 polymerase

Investigator: MT

Aim of the experiment:

Create blunt ends, needed for ligation

Procedure:

5 µL 2x Q5 Mastermix
5 µL F386 (25.9 ng/µL)
15 min; 72 °C

Results:

F388

Ligation: F374 + F386 = F390

Investigator: MT

Aim of the experiment:

Ligation: F374 + F386

Procedure:

1 µL F374 (25.9 ng\µL)
17.5 µL F387 (~ 22 ng\µL)
2 µL buffer
1 µL T4 ligase
30 min; RT

Results:

F374 + F386 = F390

Ligation: F374 + F388 = F391

Investigator: MT

Aim of the experiment:

Ligation: F374 + F388 = F391

Procedure:

0.3 µL F374 (25.9 ng\µL)
10 µL F388 (~ 13 ng\µL)
2 µL T4 ligase buffer
1 µL T4 ligase
6.7 µL ddH2O
30 min; RT

Results:

F374 + F388 = F391

Transformation of F390, F391, F376 and F377 (INSULIN)

Investigator: EU

Aim of the experiment:

Transformation of F390, F391, F376 and F377 for further application

Procedure:

3 µL DNA were added to xl1-cells
incubation on ice for 20 min
heatshock in 42°C for 40s
incubation on ice for 4 min
700µl LB-medium were added
incubation for 1h in 37°C shaker
centrifugation for 3 min

Results:

Transformation of F389 (zk-vector)

Investigator: EU

Aim of the experiment:

Transformation of F389 for further application

Procedure:

3 µL DNA were added to xl1-cells
incubation on ice for 20 min
heatshock in 42°C for 40s
incubation on ice for 4 min
700µl LB-medium were added
incubation for 1h in 37°C shaker
centrifugation for 3 min

Results:

Transformation of F366

Investigator: EU

Aim of the experiment:

Transformation of F366 for further application

Procedure:

3 µL DNA were added to xl1-cells
incubation on ice for 20 min
heatshock in 42°C for 40s
incubation on ice for 4 min
700µl LB-medium were added
incubation for 1h in 37°C shaker
centrifugation for 3 min

Results:

Friday, Sep 16th

Digestion of P430

Investigator: MT

Aim of the experiment:

Digestion of P430

Procedure:

10 µL 430 (~150 ng/µL)
2 µL CutSmart buffer
0.25 µL PacI
0.25 µL AgeI
7.5 µL ddH2O
1h; 37 °C

Results:

1kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]

P430[PacI&AgeI] -> F400 2.1 ng/µL

Digestion of P424

Investigator: MT

Aim of the experiment:

Digestion of P424

Procedure:

17 µL 424 (60.9 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
1h; 37 °C

Results:

1kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]

P424[SpeI&PstI] -> F401 15.7ng/µL

Digestion of P425

Investigator: MT

Aim of the experiment:

Digestion of P425

Procedure:

10 µL 425 (~222 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
7.5 µL ddH2O
1h; 37 °C

Results:

1kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]

P425[SpeI&PstI] -> F402 53 ng/µL

Week 19, Sep 19th - Sep 25th

Tuesday, Sep 20th

Digestion of P444; P445; P446

Investigator: MT

Aim of the experiment:

Digestion of P444; P445; P446

Procedure:

P444:

8 µL P444 (377.7 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
9.5 µL ddH2O
1h; 37 °C

P445:

14 µL P445 (223.7 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
3.5 µL ddH2O
1h; 37 °C

P446:

17.5 µL P446 (144 ng/µL)
2 µL CutSmart buffer
0.25 µL SpeI
0.25 µL PstI
1h; 37 °C

Results:

1kb ruler P451[PacI&MluI], P451[PacI&MluI], P444[SpeI&PstI], P446[SpeI&PstI]

-> I did P444 again, because there was marker in the line.

1kb ruler, P444[SpeI&PstI], P445[SpeI&PstI]

P444[SpeI&PstI] -> F420 18 ng/µL
P445[SpeI&PstI] -> F418 24.2 ng/µL
P446[SpeI&PstI] -> F421 7.4 ng/µL

Wednesday, Sep 21th

Ligation {F438 + F435} + F433 or F334

Investigator: MT

Aim of the experiment:

Ligation {F438 + F435} + F433 or F334

Procedure:

F438 + F435:

10 µL F438 (40.2 ng/µL)
11 µL F435 (30.5)
2 µL T4 Ligase buffer
1 µL T4 Ligase
6 µL ddH2O

{F438 + F435} + F433:

0.5 µL F433 (48.2 ng/µL)
4.5 µL {F438 + F435} (~24.4 ng/µL)
2 µL T4 Ligase buffer
1 µL T4 Ligase
12 µL ddH2O

{F438 + F435} + F434:

0.5 µL F434 (109 ng/µL)
4.5 µL {F438 + F435} (~24.4 ng/µL)
2 µL T4 Ligase buffer
1 µL T4 Ligase
11.5 µL ddH2O

Results:

F438 + F435 = F439
{F438 + F435} + F434 = F440
{F438 + F435} + F433 = F441

Sunday, Sep 25th

Ligation: F457 + F463 = F464

Investigator: MT

Aim of the experiment:

Ligation: F457 + F463

Procedure:

2.7 µL F457 (29.3 ng\µL)
4.3 µL F463 (22.1 ng\µL)
2 µL buffer
1 µL T4 ligase
30 min; RT

Results:

F457 + F463 = F464

Ligation: F458 + F463 = F465

Investigator: MT

Aim of the experiment:

Ligation: F458 + F463

Procedure:

3.8 µL F458 (15.5 ng\µL)
3.2 µL F463 (22.1 ng\µL)
2 µL buffer
1 µL T4 ligase
30 min; RT

Results:

F458 + F463 = F465

Ligation: F434 + F464 = F466

Investigator: MT

Aim of the experiment:

Ligation: F434 + F464

Procedure:

0.5 µL F434 (109.1 ng\µL)
6.5 µL F464 (17.4 ng\µL)
2 µL buffer
1 µL T4 ligase
over night; 16 °C

Results:

F434 + F464 = F466

Ligation: F434 + F465 = F467

Investigator: MT

Aim of the experiment:

Ligation: F434 + F465

Procedure:

0.4 µL F434 (109.1 ng\µL)
6.6 µL F465 (12.96 ng\µL)
2 µL buffer
1 µL T4 ligase
over night; 16 °C

Results:

F434 + F465 = F467

Week 20, Sep 26th - Aug 2th

@@ Line 1: / Line 1: @@
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+{{LMU-TUM_Munich|navClass=labjournal}}
 {{LMU-TUM_Munich/16style}}
 {{Team:TU-Munich/ExCol}}
 {{Team:TU-Munich/LabHeader}}
+<html>
+</div>
+<div class="col-sm-8 col-sm-offset-3">
+</html>
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-== Labjournal ==
+==Labjournal==
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@@ Line 13: / Line 16: @@
          <b>Display:</b><br>
          <input class="labcheckbox" type="checkbox" name="category" value="general" id="ui-test7" /><b style="color: rgb(115, 208, 255);">General</b><br>
-         <input class="labcheckbox" type="checkbox" name="category" value="vector_design" id="ui-test1" /><b style="color: rgb(166, 126, 166);">Streptavidin</b><br>
+         <input class="labcheckbox" type="checkbox" name="category" value="streptavidin" id="ui-test1" /><b style="color: rgb(166, 126, 166);">Streptavidin</b><br>
-         <input class="labcheckbox" type="checkbox" name="category" value="effectors" id="ui-test2" /><b style="color: rgb(116, 183, 112);">Linkers</b><br>
+         <input class="labcheckbox" type="checkbox" name="category" value="linkers" id="ui-test2" /><b style="color: rgb(116, 183, 112);">Linkers</b><br>
-         <input class="labcheckbox" type="checkbox" name="category" value="viability" id="ui-test3" /><b style="color: rgb(255, 122, 97);">Receptor</b><br>
+         <input class="labcheckbox" type="checkbox" name="category" value="receptor" id="ui-test3" /><b style="color: rgb(255, 122, 97);">Receptor</b><br>
-         <input class="labcheckbox" type="checkbox" name="category" value="safety_mechanism" id="ui-test5" /><b style="color: rgb(0, 32, 96);">Optogenetics</b><br>
+         <input class="labcheckbox" type="checkbox" name="category" value="optogenetics" id="ui-test5" /><b style="color: rgb(0, 32, 96);">Optogenetics</b><br>
+        <input class="labcheckbox" type="checkbox" name="category" value="polymerization" id="ui-test10" /><b style="color: rgb(160, 0, 39);">Polymerization</b><br>
+        <input class="labcheckbox" type="checkbox" name="category" value="hypoxia" id="ui-test11" /><b style="color: rgb(219, 48, 130);">Hypoxia</b><br>
+        <input class="labcheckbox" type="checkbox" name="category" value="kill-switch" id="ui-test12" /><b style="color: rgb(255, 255, 0);">Kill-Switch</b><br>
          <a href="#" id="ExAll">Expand All ...</a><br>
@@ Line 22: / Line 28: @@
          <b>Jump to:</b><br>
-         <a href="#Week_1">Week 1</a> 2.5-8.5<br>
+        <a href="#Week_0">Week 0</a> sample<br>
-         <a href="#Week_2">Week 2</a> 9.5-15.5<br>
+         <a href="#Week_1">Week 1</a> May 16&ndash;22<br>
-         <a href="#Week_3">Week 3</a> 16.5-22.5<br>
+         <a href="#Week_2">Week 2</a> May 23&ndash;29<br>
-         <a href="#Week_4">Week 4</a> 23.5-29.5<br>
+         <a href="#Week_3">Week 3</a> May 30&ndash;June 05<br>
-         <a href="#Week_5">Week 5</a> 30.5-5.6<br>
+         <a href="#Week_4">Week 4</a> June 06&ndash;12<br>
-         <a href="#Week_6">Week 6</a> 6.6-12.6<br>
+         <a href="#Week_5">Week 5</a> June 13&ndash;19<br>
-         <a href="#Week_7">Week 7</a> 13.6-19.6<br>
+         <a href="#Week_6">Week 6</a> June 20&ndash;26<br>
+         <a href="#Week_7">Week 7</a> June 27&ndash;July 03<br>
+        <a href="#Week_8">Week 8</a> July 04&ndash;10<br>
+        <a href="#Week_9">Week 9</a> July 11&ndash;17<br>
+        <a href="#Week_10">Week 10</a> July 18&ndash;24<br>
+        <a href="#Week_11">Week 11</a> July 25&ndash;31<br>
+        <a href="#Week_12">Week 12</a> Aug 01&ndash;07<br>
+        <a href="#Week_13">Week 13</a> Aug 08&ndash;14<br>
+        <a href="#Week_14">Week 14</a> Aug 15&ndash;21<br>
+        <a href="#Week_15">Week 15</a> Aug 22&ndash;28<br>
+        <a href="#Week_16">Week 16</a> Aug 29&ndash;Sep 04<br>
+        <a href="#Week_17">Week 17</a> Sep 05&ndash;11<br>
@@ Line 35: / Line 52: @@
          <div id="ladder" class="ui-widget ui-widget-content ui-corner-right">
-         <b><u>1 kbp GeneRuler:</u></b><br>
+         <br><b>1 kbp GeneRuler:</b><br><br>
          <img src="https://static.igem.org/mediawiki/2012/e/e3/TUM12_1000bp.jpg"></img><br>
-         <b><u>100 bp GeneRuler:</u></b><br>
+         <br><b>100 bp GeneRuler:</b><br><br>
          <img src="https://static.igem.org/mediawiki/2012/d/da/TUM12_100bp.jpg"></img><br>
-         <b><u>PageRuler Plus:</u></b><br>
+         <br><b>PageRuler Plus:</b><br><br>
          <img src="https://static.igem.org/mediawiki/2012/8/8c/TUM12_250kDa.jpg"></img><br>
          </div>
@@ Line 47: / Line 64: @@
 </div>
-=Week Test=
+=Samples=
-<div class="week" id="WWeek_1">
+<div class="week" id="Week_0">
-=='''Monday, April 22nd'''==
-<div class="safety_mechanism">
+<div class="linkers">
-===  Transformation of ''E.&nbsp;coli'' XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3) ===
+===  Transformation of ''E.&nbsp;coli'' XL1 blue with Phytochrome B (2&ndash;908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3) ===
 '''Investigator: Jeff, Rosario'''
-'''Aim of the experiment:''' Transformation of Phytochrome B for protein fusion.
+'''Aim of the experiment:''' Transformation of Phytochrome B for protein fusion
 '''Procedure:'''
-* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
-* 2&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 2&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
 * 30&nbsp;min incubation on ice
-* 5&nbsp;min. heat shock at 37&nbsp;°C
+* 5&nbsp;min heat shock at 37&nbsp;°C
-* Adding of 1&nbsp;ml LB-medium to each tube.
+* Added 1&nbsp;ml LB medium to each tube
-* Incubation for 45&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker.
+* Incubation for 45&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
-* 100&nbsp;µl of the cell suspension was plated on one chloramphenicol plate.
+* 100&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
-* The rest were centrifuged for 1&nbsp;min at 13000&nbsp;rpm and the supernatant was dicarded.
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
 * The pellet was resuspended in 100&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate.
@@ Line 105: / Line 121: @@
 </div>
-=='''Tuesday, April 23rd'''==
+<div class="optogenetics">
-<div class="safety_mechanism">
 === Picking of of ''E.&nbsp;coli'' XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3) ===
@@ Line 234: / Line 248: @@
 </div>
-=='''Wednesday, April 24th'''==
+<div class="receptor">
-<div class="safety_mechanism">
 ===  Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)  ===
@@ Line 250: / Line 262: @@
 </div>
-<div class="safety_mechanism">
+<div class="linkers">
 === Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10 ===
@@ Line 381: / Line 393: @@
 </div>
-<div class="effectors">
+<div class="linkers">
 ===  Transformation of ''E.&nbsp;coli'' XL1 blue with  ===
@@ Line 410: / Line 422: @@
 <!--- PLEASE DO NOT TOUCH !!!! -->
-=Week 2=
+=Week 1, May 16th - May 22nd=
-<div class="week" id="WWeek_2">
+<div class="week" id="Week_1">
-=='''Thursday, June 23rd'''==
-<div class="Receptor">
+=='''Monday, May 16th'''==
+<div class="streptavidin">
+=== Streptavidin Plasmid Check  ===
+'''Investigator: JB, LK, JH'''
+'''Aim of the experiment:''' Verify cloning
+'''Procedure:'''
+* MiniPrep following manufacturer's protocol (QIAprep MiniPrep, Qiagen) (4 clones each of pSA1, pSAm1 in pASK75)
+* Analytic digestion with 0.25 ''µ''L XbaI, 0.25 ''µ''L HindIII (HF), 1 ''µ''L SmartCut Buffer, 5 ''µ''L plasmid DNA, 3.5 ''µ''l H<sub>2</sub>O
+* 5 ''µ''L analyzed in gel electrophoresis (1% agarose)
+'''Results:''' Successful cloning verified. Stored at &ndash;20 °C
+* Lane 1: 5 ''µ''L Thermo Fisher, 1 kb ladder
+* Lanes 2&ndash;9: 5 ''µ''L digestions of P6&ndash;P13, band of SA (mut1) at about 300 bp, band of digested plasmid at about 3,000 bp
+[[File:Muc16_P6_to_P13_SA_mut1.png|500px]]
+</div>
+<div class="streptavidin">
+=== Streptavidin Expression: Transform BL21  ===
+'''Investigator: JB, JH'''
+'''Aim of the experiment:''' Express pSA1 and pSAm1 in ''E. coli'' BL21
+'''Procedure:'''
+* Transformation into competent ''E. coli'' BL21 according to protocol of P6 and P10
+'''Results:''' Plates (LB Amp) in incubator (37 °C) for further processing
+</div>
+=='''Tuesday, May 17th'''==
+<div class="general">
+=== SDS Gel Analysis  ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Analyze collagen 1/2, eGFP, fraction 30 of egg precipitation ''via'' SDS gel
+'''Procedure:'''
+* Mixed 80 ''µ''L samples with 20 ''µ''L SDS buffer
+* Heated at 95 °C for 10 min
+* 1 d staining, 1 d unstaining
+'''Results:''' Successful cloning verified. Stored at &ndash;20 °C
+* Lane 1: 8 ''µ''L marker (Thermo Fisher #26610)
+* Lane 2: Fraction 30 (IEC), 3 ''µ''L, band at 35 kDa, avidin expected at 16 kDa
+* Lane 3: eGFP, 12 ''µ''L, band at 27 kDa, eGFP expected at 27 kDa, many impurities
+* Lane 4: Collagen 1, 12 ''µ''L, no sharp band
+* Lane 5: Collagen 1, 12 ''µ''L, no sharp band
+[[File:Muc16_SDS_gel_analysis_fraction_30_of_egg-precipitation.png|500px]]
+</div>
+<div class="general">
+=== MiniPreps pSb1C3&ndash;AviTag, &ndash;A3C5 and pASK75&ndash;(SA1), &ndash;(SAm1)  ===
+'''Investigator: CR, CG'''
+'''Aim of the experiment:''' Verify cloning
+'''Procedure:'''
+* MiniPrep was performed following manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Analytic digestion with 0.25 ''µ''L XbaI, 0.25 ''µ''L HindIII (HF) for pASK plasmids and 0.25 ''µ''L NgomIV, 0.25 ''µ''L AgeI (HF) for pSb1C3 plasmids, 1 ''µ''L SmartCut Buffer, 5 ''µ''L plasmid DNA, 3.5 ''µ''L H<sub>2</sub>O
+* 5 ''µ''L on 1% agarose gel electrophoresis
+'''Results:''' Successful cloning verified for pASK plasmids. Repeat pSb1C3 plasmids. Stored at &ndash;20 °C
+* Lane 1: 5 ''µ''L Thermo Fisher, 1 kb Ladder
+* Lane 2: 5 ''µ''L digestion of pSb1C3&ndash;AviTag
+* Lane 3: 5 ''µ''L digestion of pSb1C3&ndash;A3C5
+* Lane 5: 5 ''µ''L digestion of pASK75(SA1), EB elution
+* Lane 6: 5 ''µ''L digestion of pASK75(SAmut1), EB elution
+* Lane 7: 5 ''µ''L digestion of pASK75(SAmut1), H<sub>2</sub>O elution
+[[File:Muc16_verification_pASK.png|500px]]
+</div>
+<div class="streptavidin">
+=== Inoculation of Pre-Culture with BL21 (pASK75 (SA1)) in LB Medium   ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Pre-culture for streptavidin expression in TB medium
+'''Procedure:'''
+* Added 50 ''µ''L ampicillin to 50 mL LB medium
+* Picked colonies from BL21 (pASK75 (SA1))
+* Inoculated LB medium
+* Incubated at 30 °C overnight
+</div>
+=='''Wednesday, May 18th'''==
+<div class="general">
+=== Repeat Analytical Gel of pSb1C3&ndash;AviTag, &ndash;A3C5  ===
+'''Investigator: CG, CR'''
+'''Aim of the experiment:''' Verify cloning
+'''Procedure:'''
+* Analytic digestion with 0.25 ''µ''L NgoMIV, 0.25 ''µ''L AgeI (HF) for pSb1C3 plasmids, 1 ''µ''L SmartCut Buffer, 8.5 ''µ''L plasmid DNA
+* 10 ''µ''L analyzed in gel electrophoresis (2% agarose)
+'''Results:'''
+[[File:Muc16 Repetition of analytical gel of pSb1C3-AviTag,-A3C5.png|500px]]
+</div>
+<div class="streptavidin">
+=== Inoculation of BL21 (pASK75 (SA1)) Culture in 2 L TB Medium and Induction of Streptavidin Production by Addition of Tetracycline  ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Produce streptavidin
+'''Procedure:'''
+* Ampicillin (2 mL) was added to the medium (1:1000)
+* The pre-culture (50 mL) was poured into the medium
+* Culture incubated at 37 °C and 140 rpm until OD<sub>550</sub> reached 0.5
+* To induce streptavidin expression, anhydro-tetracycline (200 ''µ''L) was added to the culture (1:10,000)
+* The culture was incubated at 37 °C and 140 rpm for 4 hours
+'''Results:''' Streptavidin expression by BL21
+</div>
+<div class="streptavidin">
+=== Expression and Harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB Medium   ===
+'''Investigator: CR, JB, JH '''
+'''Aim of the experiment:''' Recombinant expression and purification of streptavidin
+'''Procedure:'''
+* After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
+* The supernatant was discarded, and the pellet was transferred into a beaker of sufficient size and resuspended in Tris Buffer B cooled to 4 °C (50 mM Tris/HCl pH = 8.0, 1 mM EDTA)
+* The solution was homogenized in the PANDA (ask supervisor)
+* The resulting lysate was transferred into centrifuge tubes and spun down (4 °C, 18,000 rpm, 10 min, XX34-rotor). The supernatant was discarded, and the pellet was resuspended in 6 M Gua-HCl (pH = 1.5) at 4 °C overnight.
+</div>
+<div class="polymerization">
+=== Dialysis of eGFP ===
+'''Investigator: NA, JH, CR '''
+'''Aim of the experiment:''' Purify eGFP
+'''Procedure:'''
+* eGFP was thawed on ice
+* eGFP was then poured into a dialysis hose (cut-off 14 kDa)
+* The hose was then placed in ice-cold Tris/HCl 20 mM pH 8.0
+* Dialyzed at 4 °C overnight (XX34 rotor). The supernatant was discarded, and the pellet was
+</div>
+<div class="receptor">
+=== MiniPrep of quickchanged pNGAL146-A2 EspP  ===
+'''Investigator: NA '''
+'''Aim of the experiment:''' Extraction of pNGAL146-A2 plasmid from XL1 blue
+'''Procedure:'''
+* MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+</div>
+<div class="receptor">
+=== Sequencing of P14 (Avi-Tag), P15 (A3C5) & P19 (Quick change (QC) EspP in pNGAL-A2)   ===
+'''Investigator: CR, NA '''
+'''Aim of the experiment:''' Sequencing of P14 (Avi-Tag), P15 (A3C5) & P19 (Quick change (QC) EspP in pNGAL-A2)
+'''Procedure:'''
+* Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+* The different plasmids we prepared received the following barcodes:
+* P14        : FR11326653
+* P15        : FR11326655
+* P19 (K4): FR11326654
+* P16 (K1): FR11326652
+* P17 (K2): FR11326651
+* P18 (K3): FR11326650
+</div>
+<div class="receptor">
+=== Digestion of P16 , P17, P18 & P19 (all QC EspP in pNGAL-A2) with AgeI & HindIII + analytical gel  ===
+'''Investigator: NA, JH, CR '''
+'''Aim of the experiment:''' Verification of success of quickchange
+'''Procedure:'''
+* analytic digestion with: 0,25 µl HindIII (HF), 0,25 µl AgeI (HF), 1 µl SmartCut Buffer, 500 ng plasmid-DNA, fill up with ddH2O (Vtotal= 10µL)
+* 10 µl on 2% agarose gel for electrophoresis
+'''Results:''' No signal at 600 bp --> quickchange seems to be successful (waiting for sequencing)
+[[File:Muc16_Verification_of_success_of_quickchange.png|500px]]
+</div>
+=='''Thursday, May 19th'''==
+<div class="streptavidin">
+===Re-Sequencing of P19===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Re-Sequencing of P19
+'''Procedure:'''Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+The different plasmids we prepared received the following barcodes:
+*P19 (K4): FR11326649
+</div>
+<div class="receptor">
+===Cloning of A3C5 and Avi-Tag into pSB1C3===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Re-Trafo of pSB1C3 RFP for later on: digestion, dephosphorylation and cloning
+'''Procedure:''' transformation according to protocol of P4 E. Coli XL1
+'''Result:''' plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+<div class="streptavidin">
+===Streptavidin refolding===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Refolding of denaturated Streptavidin
+'''Procedure:''' After the pellet had almost completely dissolved in 6M GdmCl, the solution was spun down (4°C, 20 mins, 18,000 rpm). The supernatant was transferred carefully into a falcon tube and the pellet was cast away. Via a hydraulic pump (flow rate: 2x10 ml/min) the lysate was transferred Into 5L PBS 1x. Afterwards the pump was cleaned with technical isopropanol and ELGA water. The solution was stirred overnight at 4°C for refolding.
+</div>
+<div class="polymerization">
+===Biotinylation of BSA===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Biotinylation of BSA
+'''Procedure:''' A 100 µM (=6.8 mg/ml) solution of BSA (Albumin fraction V, pH=7, in the fridge in the central lab) was created (V=10 ml). 220 µl of a 100 mM Biotin stock were added. The mixture was stored overnight Iin the fridge (4°C).
+'''Result:''' Hopefully biotinylated BSA mixture in the fridge (4°C).
+</div>
+=='''Friday, May 20th'''==
+<div class="streptavidin">
+=== Qualitative analysis of streptavidin expression ===
+'''Investigator: CG '''
+'''Aim of the experiment:''' SDS gel analysis of recombinant strepatividin expression
+'''Procedure:'''  mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining
+'''Result:'''
+* 1. Lane: 8 µl Marker (Thermo Fisher #26610)
+* 2. Lane: 12 µl culture aliquot, before induction
+* 3. Lane: 12 µl culture aliquot, after induction
+* 4. Lane: 3 µl culture aliquot of the lysed pelet, Strepatvidin expected at about 16 kDa
+* 5. Lane: 3 µl culture aliquot of the supernatend after lysis, no Strepatvidin expected at about 16 kDa
+* 6. Lane: 1.5 µl culture aliquot of the lysed pelet, Strepatvidin expected at about 16 kDa
+* 7. Lane: 1.5 µl culture aliquot of the supernatend after lysis, no Streptavidin expected at about 16 kDa
+[[File:Muc16_SDS_gel_analysis_of_recombinant_strepatividin_expression.png|500px]]
+</div>
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Inoculation of pre-culture with E. coli XL1 (pSb1C3 -RFP) in LB-Chloramphenicol-medium
+'''Procedure:'''
+Picking of colonies for E. coli XL1 (pSb1C3 -RFP)
+Inoculate in 5 ml LB-Chloramphenicol-medium
+Incubate at 37°C over night at 200 rpm
+</div>
+<div class="receptor">
+=== Transformation of Biobricks in XL1-blue ===
+'''Investigator: NA, JH'''
+'''Aim of the experiment:''' Transformation
+'''Procedure:'''
+-10 µl dd H2O in well of interest (standard distribution kit)
+-1 µl Plasmid (out of well) to cells
+-Transformation according to the SOP
+Used bricks:
+K577893, B0015, R0040, B0032, I14033, K747096
+</div>
+<div class="streptavidin">
+=== Ammonium sulfate precipitation of streptavidin ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Reduction of the protein solution volume and precipitation of streptavidin
+'''Procedure:''' The 5 L protein solution was spun down (20 mins, 5,000 rpm) and the supernatant transferred into a beaker. In order to lower the volume of the solution for ammonium sulfate precipitation, the solution was first filtered via a membrane crossflow pump (membrane: Sartocon 0.45 µm, thick membrane).
+</div>
+<div class="polymerization">
+=== Dialysis of biotinylated BSA ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' purification of biotinylated BSA
+'''Procedure:''' dialysis against Tris/HCl 20 mM, pH 8, 10 mM NaCl over night;
+cut off : 14 kDa
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 2 (May 23rd - May 29th)=
+<div class="week" id="Week_2">
+=='''Monday, May 23th'''==
+<div class="receptor">
+===Cloning of A3C5 and Avi-Tag into pSB1C3===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Cloning of A3C5 and Avi-Tag into pSB1C3
+'''Procedure:'''
+* MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* pSB1C3 was digested with AgeI and NgOMIV (10 µL plasmid + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 14 µL ddH2O; incubation for 1h, 37°C)
+* FastAP was added and the reaction was incubated for another 2h at 37°C
+* The digestion was purified by gelelctrophoresis (1%, 75V, 1h)
+* Plasmid backbone was cut from the gel
+'''Results:'''
+[[File:Muc16_Cloning_of_A3C5_and_Avi-Tag_into_pSB1C3.png|500px]]
+Signal 1: linearized pSB1C3 (successfull digestion)
+Signal 2: supercoiled pSB1C3 (digestion not successfull)
+Signal 3: RFP-generator
+--> next time gel should run longer (just if you need the back bone)
+</div>
+<div class="streptavidin">
+=== Filtration of Streptavidin and precipitation with Ammonium-sulfate ===
+'''Investigator: MP, CR'''
+'''Aim of the experiment:''' Concentration of Streptavidin
+'''Procedure:'''
+The solution was filtered via a membrane crossflow pump (membrane: Sartocon 0.45 µm, thick membrane).
+The final volum was 0.5L
+The solution was precipitated by addition of Ammonium-sulfate (2 steps: 1. 40% Ammonium-sulfate; 2. 70% Ammonium-sulfate)
+After the first addition of ammonium-sulfate the solution was stirred (1h, 4°C)
+Afterwards the solution was centrifuged (10.000 rpm; 30 min) and the supernatant was used for the second precipitation step
+The solution was stirred again (over night, 4°C)
+</div>
+<div class="general">
+=== Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam ===
+'''Investigator: JH, JL'''
+'''Aim of the experiment:'''
+'''Procedure:'''
+Add 50 µL chloramphenicol in 50 mL LB-medium
+Picking colonies from K577893; B0015; B0032 (in pSB1C3) *
+Inoculate 4 mL medium (CAM)
+Incubate at 37°C over night
+*Following cultures didn´t grow and were therefore not inoculated:
+R0040; K747096; I14033
+</div>
+<div class="general">
+=== Retransformation of Biobricks in XL1-blue===
+'''Investigator: JH, JL, EF'''
+'''Aim of the experiment:''' Transformation
+'''Procedure:'''
+µl dd H2O in well of interest (standard distribution kit)
+µl Plasmid (out of well) to cells
+Transformation according to the SOP
+Used bricks:
+K577893, B0015, R0040, B0032, I14033, K747096
+</div>
+=='''Tuesday, May 24th'''==
+<div class="general">
+=== Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam ===
+'''Investigator: CR'''
+'''Aim of the experiment:'''
+'''Procedure: '''
+Add 50 µL chloramphenicol in 50 mL LB-medium
+Picking colonies from K577893; B0015; B0032 (in pSB1C3) *
+Inoculate 4 mL medium (CAM)
+Incubate at 37°C over night
+</div>
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Gelextraction of Signal 1 from pSB1C3-digestion
+'''Procedure:'''
+Gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen)
+</div>
+<div class="streptavidin">
+=== Ammonium sulfate precipitation ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Precipitation the 70% saturated ammonium sulfate solution
+'''Procedure:'''   The ammonium sulfate solution, which actually was a suspension, was transferred into centrifuge tubes and spun down (10,000 rpm, 45 mins). As it turns out, unfortunately too much ammonium sulfate was used for the precipitation (wrong table). The precipitate was brought back into solution (20 mM  Tris/HCl, pH 8.0) and loaded onto an SDS gel for analysis, along with other samples (flowthrough of the filtration from the day before).
+</div>
+<div class="general">
+=== MiniPrep of BioBricks in pSB1C3 (inoculated on May 23th) ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Extraction of BioBricks B0032, B0015 and K577893 in pSB1C3 from XL1 blue
+'''Procedure:'''
+MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+concentrations measured (in ng/µL):
+(B0032) 360.2; (B0015) 254.9; (K577893) 99.2
+</div>
+<div class="general">
+=== Sequencing of P23 (weak RBS), P24 (double terminator) & P24 (Tet repressed GFP) ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Sequencing of P23, P24 & P25 (x2)
+'''Procedure:'''
+Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+The different plasmids we prepared received the following barcodes:
+* P23  (VF2) : FR11326647
+* P24  (VF2) : FR11326646
+* P25  (VF2) : FR11326645
+* P25  (VR) : FR11326644
+</div>
+=='''Wednesday, May 25th'''==
+<div class="receptor">
+=== Inoculation of pre-culture with tet-repressed GFP (P25) in LB-Cam ===
+'''Investigator: NA'''
+'''Procedure:'''
+Add 50 µL chloramphenicol to 50 mL LB-medium
+Picking colonies from plate (BL21)
+Incubate over night at 37°C
+=> dismissed, because plasmid sequence was inaccurate
+</div>
+<div class="general">
+=== MiniPrep of K747096, I14033, R0040, B0015,  K577893 and B0032 ===
+'''Investigator: CR'''
+'''Aim of the experiment: MiniPrep of BioBricks'''
+'''Procedure:'''
+MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+Concentrations were measured (in ng/µL):
+* K747096: 	286.2
+* I14033: 	246.1
+* R0040: 	243.5
+* B0015: 	244.1
+* K577893: 	440.9
+* B0032: 	259.7
+</div>
+<div class="receptor">
+=== PCR of P19 (QC EspP) with O3 and O4 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Amplification of quickchanged EspP
+'''Procedure:'''
+*reaction was performed after manufacturer's protocol (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
+*274,4 pg Plasmid were used for amplification (1 µL)
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial Denaturation||98||30
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|72||30
+|-
+|72||60
+|-
+|final Extension||72||5
+|-
+|Hold||4||ꝏ
+|}
+* PCR product was purified accoding to manufacturer's protocol (PCR puification kit, Qiagen)
+* DNA was eluted 40 µL EB buffer
+</div>
+<div class="receptor">
+=== Digestion of PCR of EspP (P19 with O3 and O4) ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Digestion of EspP with AgeI and NgoMIV to ligate it in pSB1C3 later on
+'''Procedure:'''
+* Batch for preparative digestion:
+{|cellspacing="0" border="1"
+|'''Volume'''
+|'''Reagent'''
+|-
+|38.5 µL||PCR product P19 with O3 and O4
+|-
+|1 µL||AgeI
+|-
+|1 µL||NgoMIV
+|-
+|5 µL||CutSmart buffer
+|-
+|4.5 µL||ddH<sub>2</sub>O
+|-
+|50 µL||TOTAL
+|}
+* Incubation for 2 h at 37 °C
+</div>
+<div class="receptor">
+=== Sequencing of P26 (CMV promotor), P27 (p cat promotor), P28 (Tet repressible promotor), P30 (Tet repressed GFP) ===
+'''Investigator: NA'''
+'''Aim of the experiment:'''
+Sequencing of P26, P27, P28 & P30 (x2)
+'''Procedure:'''
+Sequencing batches were prepared after manufacturer's protocol
+(15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer)
+The different plasmids we prepared received the following barcodes:
+P26 (VF2) : FR11326643
+P27 (VF2) : FR11326642
+P28 (VF2) : FR11326641
+P30 (VF2) : FR11326640
+P30 (VR): FR11326639
+</div>
+<div class="polymerization">
+=== Ion exchange chromatography of eGFP ===
+'''Investigator: NA, JB,JL'''
+'''Aim of the experiment:''' purification of eGFP
+'''Procedure:'''
+* use Äkta-Purifier (Q-column for eGFP (quarternary ammonium as stationary phase)). Ask Andy before use!
+* Pump A: running buffer (20 mM Tris/HCl pH 8); pump B: elution buffer (20 mM Tris/HCl pH 8 and  1,000 mM (1 M) NaCl
+* basic pumpwash before start
+* injection in loop
+* gradient of ion strength on column.
+'''Results:'''
+Elution of eGFP at ~200 mM NaCl.
+[[File:Muc16_elution_of_eGFP.png|500px]]
+</div>
+=='''Thursday, May 26th'''==
+<div class="general">
+=== Inoculation of cultures with XL-1 F11 and F12 clones ===
+'''Investigator: JB'''
+'''Aim of the experiment:'''
+Inoculation of a 5 ml culture with a clone of the previously transformed F11 (Avi-Tag) F12 (Antibody-binding site).
+</div>
+<div class="general">
+=== Cloning of ligation F14 +F13 ===
+'''Investigator: MP, EF, JH'''
+'''Aim of the experiment:''' new biobrick EspP in pSB1C3
+'''Procedure:'''
+F14 was purified by gelelctrophoresis (1%, 90 V, 40 min)
+gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen)
+ligation of F14 (EspP) with F13 (dephos. PSB1C3)
+transformation according to protocol in competent E.coli XL1 blue
+'''Results:'''
+[[File:Muc16_F14_gelextracion.png|500px]]
+</div>
+<div class="general">
+=== Transformation of Biobrick B0034 in XL1-blue ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Transformation
+'''Procedure:'''
+* 10 µl ddH2O in well of interest (standard distribution kit, plate 4, well 1N)
+* 1 µl Plasmid (out of well) to cells
+* Transformation according to the SOP (incl. rescue)
+</div>
+<div class="general">
+<div class="receptor">
+=== Transformation of Biobricks K577895 and K577894 in XL1-blue ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Transformation
+'''Procedure:'''
+* 10 µl ddH2O in well of interest (standard distribution kit, plate 1, wells 14B / 12P)
+* 1 µl Plasmid (out of well) to cells
+* Transformation according to the SOP (incl. rescue)
+</div>
+=== SDS-PAGE of  eGFP-fractions after IEC ===
+'''Investigator: NA, CG'''
+'''Procedure:'''  mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining
+Concentrations were measured via nanodrop (A280, extinction coefficient: 55000 M−1cm−1)
+'''Result:''' concentrations in mg/ml
+. Lane: 8 µl Marker
+. Lane: 10 µl of fraction 10; c= 0
+. Lane: 10 µl of fraction 11; c= 0,15
+. Lane: 10 µl of fraction 12; c= 0,77
+. Lane: 10 µl of fraction 13; c= 0,29
+. Lane: 10 µl of fraction 14; c= 0,4
+. Lane: 10 µl of fraction 15; c= 0,144
+. Lane: 10 µl of fraction 16; c= 0,085
+[[File:Muc16_SDS-PAGE_of_eGFP-fractions_after_IEC.png|500px]]
+eGFP is clearly detectable at about 27 kDa. The most pure fractions 12 and 13 were pooled for later biotinylation.
+</div>
+=='''Friday, May 27th'''==
+<div class="general">
+=== Inoculation of pre-cultures with B0034 (strong RBS), K577894 (Tet repressed YFP), KK577895 (Tet repressed RFP), F13+F14 ===
+'''Investigator: JH'''
+'''Procedure:'''
+* Add 50 µL ampicillin(B0034)/chloramphenicol(K5777894, K577895, F13+F14) to 50 mL LB-medium
+* Picking colonies from plate (XL1 blue; all rescue)
+* Incubate over night at 37°C
+</div>
+<div class="streptavidin">
+=== Inoculation of BL21 (pASK75 (SA1)) culture in 2 L TB-Medium and induction of streptavidin production by addition of tetracycline ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Production of streptavidin
+'''Procedure:'''
+* Ampicillin (2 mL) was added to the Medium (1:1000)
+* The pre-culture (50 mL) was poured into the Medium
+* Culture was incubated at 37°C and 140 rpm until OD550 reached 0.5
+* To induce streptavidin expression anhydro-tetrazycline (200 µL) was added to the culture (1:10000)
+* The culture was incubated at 37°C and 140 rpm for 4 hours
+'''Result:'''
+Streptavidin expression by BL21
+</div>
+<div class="receptor">
+=== Re-sequencing of P30 (Tet repressed GFP in pSB1C3) ===
+'''Investigator: NA'''
+'''Aim of the experiment:'''
+Purification and sequencing of P30
+'''Procedure:'''
+* P30 was heated up to 100 °C and centrifugated afterwards to remove proteins from Promotor (if there are some), the supernatant is sequenced
+* Sequencing batches were prepared after manufacturer's protocol
+*(15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer)
+*The different plasmids we prepared received the following barcodes:
+**P30 (VF2) : FR11326638
+</div>
+<div class="streptavidin">
+=== Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium ===
+'''Investigator: JH, NA '''
+'''Aim of the experiment:''' Recombinant expression and purification of Streptavidin
+'''Procedure:'''
+* After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4°C, 5000 rpm, 20 mins, F 4X1L rotor)
+* The supernatant was cast away and the pellet was stored at –20 °C
+</div>
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' MiniPrep of cloned pSB1C3-A3C5 and –AviTag Plasmids
+'''Procedure:'''
+* MiniPrep of inoculated precultures was performed according to manufacturer’s protocol (QIAprep MiniPrep, Qiagen)
+* Concentrations were measured (in ng/µL):
+Colony 1 of pSB1C3- AviTag P32: 	120
+Colony 2 of pSB1C3- AviTag P33: 	110
+Colony 1 of pSB1C3-A3C5 P34: 		126
+Colony 2 of pSB1C3-A3C5 P35: 		188
+</div>
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: NA, JH, CG'''
+'''Aim of the experiment:''' Initial vector digestion was performed with NgoMiV and AgeI, producing complementary overhangs. Religated pSB1C3 (due to incomplete vector dephosphorylation) loses the AgeI recognition sequence. Therefore plasmids without insert should run in the supercoiled position at about 1.5 kb, plasmids with inserts  should run in the linearised position at 3 kb. Single enzyme digestion was chosen, because the insert is too small to be solved on a gel.
+'''Procedure:'''
+* analytic digestion: 3 µl of plasmid DNA P32 to P35 (about 300 ng) were digested with 0.3 µl AgeI-HF in 1 µl CutSmart Buffer and 5.7 µl H2O. The reaction was incubated for 2 h at 37°C.
+* 5 µl digestion mix were loaded on a 1% agarose gel for electrophoresis, 1 kb ladder
+'''Result:'''
+*P32 to P35 might carry the insert because they all appear in the linearized position at 3 kb
+*Therefore plasmid sequencing should confirm the result.
+Lane 1: 1 kb ladder
+Lane 3: P32
+Lane 4: P33
+Lane 5: P34
+Lane 6: P35
+[[File:Muc16_Cloning_of_A3C5_and_Avi-Tag_into_pSB1C3.png|500px]]
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 3 (May 30th - June 5th)=
+<div class="week" id="Week_3">
+=='''Monday, May 30th'''==
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: CR'''
+'''Aim of the experiment:'''
+Sequencing of P32 and P35
+'''Procedure:'''
+*Sequencing batches were prepared according to manufacturers protocol (Mix2Seq Kit, Eurofins Genomics): 15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer (10 µM)
+*The plasmids received the following barcodes:
+**P32 (VF2) : FR11326637
+**P35 (VF2) : FR11326636
+</div>
+<div class="general">
+=== Religation of F13 (digest of pSB1C3 with AgeI and NgoMIV) and transformation in XL1 blue ===
+'''Investigator: CR'''
+'''Aim of the experiment:'''
+Re-ligate digested and dephosphorylated pSB1C3 and transformation in XL1blue
+'''Procedure:'''
+* Plasmid was ligated with the T4 DNA Ligase following the manufacturer’s protocol (NEB)
+* 52 ng Vector DNA were used
+* The Ligation mix was incubated for 30 min at RT
+* 7 μL Ligation mixed were used for the transformation of 50 μL XL1 blue.
+* Transformation was performed following the SOP
+'''Result:'''
+*5 clones on plate
+</div>
+<div class="general">
+=== Inoculation of pre-cultures with B0034 (strong RBS), K577894 (TET repressed YFP), KK577895 (Tet repressed RFP), F13+F14 ===
+'''Investigator: CR'''
+'''Procedure:'''
+* Add 50 µL ampicillin(B0034)/chloramphenicol(K5777894, K577895, F13+F14) to 50 mL LB-medium
+* Picking colonies from plate (XL1 blue; all rescue)
+* Incubate over night at 37°C
+</div>
+=='''Tuesday, May 31th'''==
+<div class="polymerization">
+=== Dialysis of eGFP ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Changing the buffer of eGFP for biotinylation (from TRIS to PBS)
+'''Procedure:'''
+* eGFP was poured in a dialysis hose (cut-off 14 kDa)
+* The hose was then placed in ice cold PBS pH 7.4
+* The dialysis took place at 4°C overnight
+</div>
+<div class="streptavidin">
+=== Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium ===
+'''Investigator: JB, NA'''
+'''Aim of the experiment:''' Recombinant expression and purification of Streptavidin
+'''Procedure:'''
+* The pellet was transferred into a beaker of sufficient size and resuspended in fridge-cooled Tris Buffer B (50 mM Tris/HCl (pH = 8.0), 1 mM EDTA)
+* The solution was homogenized in the PANDA (see SOP)
+* The resulting lysate was transferred into centrifuge tubes and spun down (4°C, 18,000 rpm, 30 mins, SS34-rotor). The supernatant was cast away and the pellet was resuspended in 6M Gua-HCl (pH = 1.5) at 4°C overnight.
+</div>
+<div class="receptor">
+=== Transformation of P30 (Tet repressed GFP)===
+'''Investigator: NA'''
+'''Aim of the experiment:''' expression of tet-repressed GFP in E. Coli BL21
+'''Procedure:''' transformation in competent E. Coli BL21 according to protocol
+'''Result:''' plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+<div class="receptor">
+=== Cloning of A3C5 and Avi-Tag into pSB1C3 ===
+'''Investigator: CR, JH'''
+'''Aim of the experiment:'''
+Preculture of pSB1C3 (F13+F14) was red
+See if RFP-generator is still inside the pSB1C3
+See if ligation of EspP was successful
+'''Procedure:'''
+* MiniPrep of P39 was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* pSB1C3 was digested with AgeI and NgOMIV (1.5 µL P39 + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 22.5 µL ddH2O; incubation for 2h, 37°C)
+* FastAP was added and the reaction was incubated for another 10min at 37°C
+* FastAP was inactivated by heating the mix to 75°C for 10min.
+* The digestion was purified by gelelctrophoresis (1%, 75V, 1h)
+'''Results:'''
+[[File:Muc16_P39_digest.png|500px]]
+Unknown signals.
+Repeat transformation, digestion, dephosphorylation and ligation of pSB1C3
+</div>
+<div class="general">
+=== Re-transformation of P4 (pSB1C3 (RFP-generator)) in XL1 blue ===
+'''Investigator: JH, CR'''
+'''Aim of the experiment:''' Transformation
+'''Procedure:'''
+* 2 μL P4 were used for transformation of XL1 blue
+* Transformation was performed according to SOP (incl. rescue plate)
+</div>
+<div class="general">
+=== Competent E. coli XL1 cells ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Generation of competent E.coli XL1 cells
+'''Procedure:'''
+* 5 ml LB w.o. antibiotics (sterile)
+* Inoculation of one colony of E.coli XL1 cells
+* Incubate overnight at 37°C
+</div>
+=='''Wednesday, June 1th'''==
+<div class="polymerization">
+=== eGFP Biotinylation ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Biotinylation of dialysed eGFP past IEC
+'''Procedure:'''
+* The average concentration of the pooled factions 12 and 13 should be about 0.5 mg/ml (=19 µM)
+* 10 ml of a 100 mM Biotin stock-solution was prepared (340 mg)
+* 3.5 ml of eGFP were biotinylated with 12 µl 100 µM Biotin-solution (20x molar excess)
+* Incubation at 4 °C overnight
+</div>
+<div class="general">
+=== pSB1C3 vector backbone preperation ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Inoculation of two colonies pSB1C3-RFP Generator
+'''Procedure:'''
+* 2x 5 ml LB+Cam medium (1:1000)
+* Picking colonies from plate (XL1 blue, rescue)
+* Incubate overnight at 37°C
+</div>
+<div class="general">
+=== Generation of GFP expressing E. coli cells ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Inoculation of BL21 transformed cell with P30
+'''Procedure:'''
+* 50 ml LB+Cam medium (1:1000)
+* Picking colonies from plate (BL21, rescue)
+* Incubate over night at 37°C
+</div>
+<div class="general">
+=== Competent E. coli XL1 cells ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Generation of competent E. coli XL1 cells
+'''Procedure:'''
+* Inoculated 500 µl preculture in 50 ml LB media w.o. antibiotics
+* Incubated and shaken at 37°C until the OD550 reached 0.44
+* Transferred into a falcon tube and incubated on ice for 10 mins
+* Spun down at 3000 g for 10 mins at 4°C, supernatant cast away
+* Pellet resuspended in 40 ml fridge-cooled MgCl2 (100 mM), once again spun down at 4°C for 10 mins at 3000 g
+* Supernatant cast away, pellet resuspended in 20 ml cold CaCl2 (50 mM)
+* Incubation on ice for 30 mins
+* Centrifugation repeated, supernatant cast away
+* Pellet resuspended in 2 ml of CaCl2 (50 mM) and glycerol (15%)-solution, aliquoted (50 µl each), frozen in liquid nitrogen and stored at -80°C for further use
+</div>
+<div class="receptor">
+=== Cloning of Pcat-RBS-construct in pSB1A2 ===
+'''Investigator: CG, JH, CR'''
+'''Aim of the experiment:''' Pcat (I14033) was cut out of P27 and ligated into P38 for generating the Pcat-RBS (B0034) construct.
+'''Procedure:'''
+* P27 was digested with EcoRI and SpeI (4 µL P27 + 1.5 µL EcoRI + 1.5 µL SpeI + 3 µL CutSmart + 20 µL ddH2O; incubation for 2h, 37°C)
+* P38 was digested with EcoRI and XbaI (10 µL P27 + 1.5 µL EcoRI + 1.5 µL XbaI + 3 µL CutSmart + 14 µL ddH2O; incubation for 2h, 37°C)
+* Preperative gel electrophoresis was performed
+* For P27 the signal at about 50 bp was cut out and gel extracted according to manufacturer's protocol (Gelextractionkit, Qiagen): 5.9 ng/µl
+* For P30 the signal at about 2.1 kb was cut out and gel extracted according to manufacturer's protocol (Gelextractionkit, Qiagen): 8.9 ng/µl
+* Ligation according to SOP
+</div>
+<div class="streptavidin">
+=== Purification of streptavidin ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Refolding denaturized streptavidin
+'''Procedure:'''
+* the GdmCl-solved streptavidin was spun down using an SS-34 rotor (~60 min, 18,000 rpm, 4°C)
+* The supernatant containing the solved and denaturized protein was transferred into a falcon tube, the pellet cast away
+* The protein solution was slowly dripped into 4 l of cooled 1x PBS (in the 4°C room) using a hydraulic pump and stirred overnight
+</div>
+=='''Tuesday, June 2th'''==
+<div class="general">
+===Preparation of pSB1C3 for further use ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Digestion of pSB1C3 to remove RFP-generator
+'''Procedure:'''
+* MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* P40 was digested with AgeI and NgOMIV (2.5 µL P40 + 1.5 µL AgeI + 1.5 µL NgoMIV + 3 µL CutSmart + 21.5 µL ddH2O)
+* Incubation over night at 37°C
+</div>
+<div class="general">
+=== Generation of GFP expressing E. coli cells ===
+'''Investigator: CG, JH'''
+'''Aim of the experiment:''' Various inductor concentrations
+'''Procedure:'''
+* 12x 5 ml LB+Cam media were inoculated with 50 µl preculture
+* when cultures reached OD550 of 0.5, they were induced with tetrazycline-anhydride of various concentrations (0 ng/µl, 20 ng/µl, 40 ng/µl etc., 200 ng/µl)
+* t=0, =30, =90, =150, =210, =270 a 100 µl aliquot of each culture was stored at 4 °C in the refrigerator
+</div>
+<div class="polymerization">
+=== Dialysis of biotinylated eGFP ===
+'''Investigator: JH, JB'''
+'''Aim of the experiment:''' Purification of biotinylated eGFP
+'''Procedure:'''
+* eGFP was poured in a dialysis hose (cut-off 14 kDa)
+* The hose was then placed in 2 L ice cold Tris/HCl 20 mM pH 8.0
+* The dialysis took place at 4°C over night
+</div>
+<div class="receptor">
+=== Ligation of F17.1 (p(cat)) and F18 (stron RBS) and transformation in XL1 blue ===
+'''Investigator: JH'''
+'''Aim of the experiment:'''
+Ligation and transformation in XL1blue
+'''Procedure:'''
+* Plasmid was ligated with the T4 DNA Ligase following the manufacturer’s protocol (NEB)
+* 9 µL F18 (B0034 in pSB1A2; RBS) and 1 µL of F17.1 (I14033; P(cat)) were used [AmpR]
+* The Ligation mix was incubated for at least 2h at RT
+* 7 μL Ligation mixed were used for the transformation of 50 μL XL1 blue
+* Transformation was performed following the SOP [AmpR], incl. rescue plate
+</div>
+=='''Friday, June 3th'''==
+<div class="general">
+=== Cloning of F8 (A3C5), F9 (Avi-Tag) and F14 (EspP) into F20 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Cloning of A3C5, Avi-Tag and into pSB1C3
+'''Procedure:'''
+* FastAP was added and the digestion of F20 and was incubated for another 15 min at 37°C
+* The digestion was purified by gelelctrophoresis (1%, 75V, 1h)
+* Plasmid backbone (signal 1) was cut from the gel
+* Gelextraction was performed after manufacturer's protocol (Gelextractionkit, Qiagen)
+'''Results:'''
+[[File:Muc16_digestion_F20.png|500px]]
+Signal 1: F20
+[F20]= 13,8 ng/μL
+</div>
+<div class="general">
+=== Generation of GFP expressing E. coli cells ===
+'''Investigator: CG, NA'''
+'''Aim of the experiment:''' SDS PAGE for verification of successful GFP expression
+'''Procedure:'''
+* SDS electophoresis according to SOP
+* Lane  1: #12, 90 min
+* Lane  2: #12, 150 min
+* Lane  3: #12, 210 min
+* Lane  4: #12, 270 min
+* Lane 5: 8 µl
+'''Results:'''
+[[File:Muc16_Generation_of_GFP_expressing_E_coli_cells.png |500px]]
+</div>
+<div class="receptor">
+=== Inoculation of colonies from F19 (pcat-strong RBS)===
+'''Investigator: CG'''
+'''Aim of the experiment:''' three colonies were picked from yesterdays transformation
+'''Procedure:'''
+* 3x 5 ml LB+Amp media
+* Each culture was inoculated with one colony
+* Incubation at 37°C overnight
+</div>
+<div class="general">
+=== Cloning of F8 (A3C5), F9 (Avi-Tag) and F14 (EspP) into F20 (pSB1C3) ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Ligation of F21, F22 and F23 into F20 and transformation
+'''Procedure:'''
+* Ligation was performed according to the SOP with: 0.7 µl F8 (1:10) / 9.3 µl F20, 0.7 µl F9 (1:10) / 9.3 µl F20, 9.1 µl F14 / 0.9 µl F20
+* Transformation was performed according to the SOP on LB Cam-Agar
+</div>
+<div class="streptavidin">
+=== Precipitation of Streptavidin ===
+'''Investigator: NA, JB, LK'''
+'''Aim of the Experiment:''' Purification of Streptavidin
+'''Procedure:'''
+* Slowly add (NH4+)2SO42- until the concentration reaches 40% (23,1 g/100mL) while stirring
+* Let it stir over night to ensure complete precipitation
+* Centrifuge at 8500 rpm at 4°C for 15min (rotor: SLA1500), dismiss the pellet and use the supernatant for further processing
+* Slowly add (NH4+)2SO42- until the concentration reaches 70% (19,1 g/100mL) while stirring
+* Let it stir over night (slowly to avoid foaming)
+* Centrifuge at 8500 rpm at 4°C for 15min (rotor: SLA1500), dismiss the supernatant and use the pellet for further processing
+* Resuspend the protein pellet in a minimum volume of TRIS/HCl; pH 8; 20mM (NO SALT) (6 mL per pellet), the pellets where then united and titrated with Buffer until the solution became clear. Total amount of buffer: 40mL
+* Transfer to 50 mL Falcon Tubes and centrifuge at full speed for 15 min. Filter the supernatant through 45nm sterile filter and keep the pellet (rescue).
+</div>
+=='''Saturday, June 4th'''==
+<div class="general">
+===Inoculation of colonies from F21 (pSB1C3 (A3C5)), F22 (pSB1C3 (Avi-Tag)), F23 (pSB1C3 (EspP)) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' three colonies were picked from each transformation
+'''Procedure:'''
+* 3x 5 ml LB+Cam media for each fragment
+* Each culture was inoculated with one colony
+* Incubation at 37°C overnight
+</div>
+<div class="receptor">
+=== MiniPrep of F19 (pSB1A2 (pcat-strong RBS))===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Extraction of Ligation: F17+F18 (starke RBS+P(cat))
+'''Procedure:'''
+MiniPrep was performed after manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+Concentrations: K1= 66,2 ng/µl; K2= 60,2 ng/µl; K3= 104,4 ng/µl
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 4 (June 6th - June 12th)=
+<div class="week" id="Week_4">
+=='''Monday, June 6th'''==
+<div class="general">
+=== Cloning of TetR from p28 into p31 (pSB1C3(weak RBS)) ===
+'''Investigator: LK, JH, NA'''
+'''Aim of the experiment:''' Cloning TetR in front of weak RBS in pSB1C3
+'''Procedure:'''
+* Digestion of p28 with EcoR1 and Spe1 (20µl DNA, 2,5 µl each enzyme, 5µl CutSmart buffer, 20µl ddH2O) and p31 (4µl DNA, 1µl EcoRI / XbaI, 2µl, 12µl DNA) -> Incubation at 37°C for 2h.
+* Electrophoresis: 1% Agar, 15 min , 70 V (oben p31 und p41, unten p28)
+[[File:Muc16_praep_P31_p28.png|500px]]
+* Gelextraction  concentrations: p28 (F25) = 2,3 ng/µl
+p31 (F24) = 7,8 ng/µl
+* Ligation with 6,3 µl vector (F24) and 1,7 µl Insert (F25) + 1µl Buffer + 1µl Ligase  over night, 16°C
+</div>
+<div class="streptavidin">
+=== SDS-PAGE of  Streptavidin ===
+'''Investigator: NA, JH, LK'''
+'''Procedure:'''  mixing of 80 µl sample with 20 µl SDS buffer and heating at 95°C for 10 min. 1 h staining, 1 night unstaining. Concentration of streptavidin was measured via UV/VIS spectroscopy.
+c = 23,5 mg/ml
+'''Result:'''
+* 1. Lane: 8 µl Marker
+* 2. Lane: 5 µl of Streptavidin_1:10
+* 3. Lane: 5 µl of Streptavidin_1:50
+* 4. Lane: 5 µl of Pellet_1:500
+* 5. Lane: 5 µl of after 40% precipitation_1:10
+* 6. Lane: 5 µl of supernatant after 70% precipitation and centrifugation
+Successful Streptavidin production verified.
+[[File:SDS-PAGE_of_Streptavidin.png |500px]]
+</div>
+<div class="receptor">
+=== Sequencing of P41 (pSB1C3 (strongRBS-p(cat))) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Sequencing of P41
+'''Procedure:'''
+Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (100 ng/ µl) and 2 µL sequencing primer (VF2))
+The plasmids prepared received the following barcode:
+* P41        : FR11326633
+</div>
+=='''Tuesday, June 7th'''==
+<div class="receptor">
+=== Transformation of P30 (Tet repressed GFP), P36 (Tet repressed RFP), P37 (Tet repressed YFP) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Transformation of RFP, GFP and YFP in BL21
+'''Procedure:'''
+transformation in competent E. Coli BL21 according to protocol + rescue
+'''Result:'''
+plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+<div class="receptor">
+=== MiniPrep of P42 to P50, analytic digestion, sequencing ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Verification of successful cloning
+'''Procedure:'''
+MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Concentrations (ng/µl each) for P42: 260, P43: 247, P44: 181, P45: 118, P46: 261, P47: 135, P48: 148, P49: 240, P50: 299
+* Analytic digestion: 0.3 µl AgeI, 2 µl CutSmart, 6.7 µl H2O for P42, P43, P44, P45, P46, P49, P50 and 0.3 µl EcoRI, 0.3 µl PstI, 2 µl CutSmart, 6.4 µl H2O for 2 h at 37°C
+* 1% agarose gel electrophoresis
+* Sequencing: P42= FR11326632 (VF2), P45 =FR11326631 (VF2)
+'''Results:'''
+* Lane 1: 5 µl 1 kb Ladder
+* Lane 2-10: Digestion of P42 to P50. P47 and P48 are carrying the insert. All other plasmids are religated and lost their AgeI site, hence they run in the ccc position.
+[[File:Muc16_miniPrep_of_P42_to_P50.png|500px]]
+</div>
+<div class="polymerization">
+=== Dialysis of not biotinylated eGFP ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Purification of eGFP for mass determination
+'''Procedure:'''
+* eGFP was poured in a dialysis tubes
+* The tubes were then placed in ice cold ammonium acetate
+* The dialysis took place at 4°C over night
+</div>
+<div class="polymerization">
+=== Polymerisation attempts ===
+'''Investigator: JH, CR, CG, JB'''
+'''Aim of the experiment:''' Identification of optimal polymerisation conditions for biotinylated eGFP and BSA in a Streptavidin reservoir
+'''Procedure:'''
+* variate of compositions for both solutions was examined to modify density properties during “printing”
+* all compositions can be found in excel sheet
+'''Results:'''
+* no or little successful polymerization at Streptavidin concentrations of 4 mg/mL and below; immense density incompatibilities
+* sucessfull polymerization at Streptavidin concentrations of 10 mg/mL and BSA solution with approx. 15% glycerol
+* no success with biotinylated eGFP (too few Biotin molecules?!)
+</div>
+=='''Wednesday, June 8th'''==
+<div class="receptor">
+=== Sequencing of P36 (Tet repressed RFP) and P37 (Tet repressed YFP) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Sequencing of P36 and P37 in both directions
+'''Procedure:'''
+Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+The different plasmids we prepared received the following barcodes:
+* P36 (VF2): FR11326630
+* P36 (VR): FR11326629
+* P37 (VF2): FR11326628
+* P37 (VR): FR11326627
+</div>
+<div class="streptavidin">
+=== Dialysis of Streptavidin ===
+'''Investigator: NA, JH'''
+'''Aim of the experiment:''' Purification of Streptavidin (possible ammonium sulfate contamination after precipitation)
+'''Procedure:'''
+* Streptavidin was poured in a dialysis hose (cut-off 14 kDa)
+* The hose was then placed in 3 L ice cold Tris/HCl 20 mM pH 8.0 (no salt)
+* The dialysis took place at 4°C over night
+</div>
+<div class="polymerization">
+=== Polymerisation attempts ===
+'''Investigator: JH, JB'''
+'''Aim of the experiment:''' Identification of optimal polymerisation conditions for biotinylated BSA in a Streptavidin reservoir
+'''Procedure:'''
+* variate of compositions for both solutions was examined to modify density properties during “printing” (Streptavidin at 10 mg/mL or higher)
+* all compositions can be found in excel sheet
+</div>
+=='''Thursday, June 9th'''==
+<div class="general">
+=== Generation of GFP, YFP, RFP expressing E. coli cells ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Various inductor concentrations, various fluorescent proteins were expressed in E coli cells
+'''Procedure:'''
+* 3x 5 ml LB+Cam media were inoculated with 50 µl preculture of GFP (P30), RFP (P36), YFP (P37)
+* when cultures reached OD550 of 0.5, they were induced with anhydro-tetrazycline of various concentrations (0 ng/µl, 100 ng/ml, 200 ng/ml)
+* 50 ng/ml = 12,5 µl of 1:100 2 mg/ml stock solution, 200 ng/ml = 50 µl of 1:100 2 mg/ml stock solution
+* t=0, =4 h and stored on ice
+'''Resuts:''' no fluorescent could be detected. Therefore an overnight induction at 37°C with 1 µM/ml inductor concentration was performed with the RFP plasmid.
+</div>
+<div class="polymerization">
+=== Biotinylation of GFP expressing E. coli cells ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Biotinylation of P30 carrying E. coli cells
+'''Procedure:'''
+* 850 µl P30 preculture from Thursday 2nd were centrifuged and the supernatend was discarded
+* Pellet was resuspended in 800 µl PBS-buffer
+* 100 µl 100 mM Biotin-NHS was added
+* incubation for 4 h at room temperature
+* Experimenting with some glycerol and streptavidin concentrations. A more structured approach will be done the next day.
+'''Results:''' A shape thin “sausage” could be detected. Therefore a bigger E. coli culture was biotinylated at 4°C overnight for experimenting with the next day.
+</div>
+<div class="receptor">
+=== Cloning of TetR promotor and weak RBS in pSB1C3 ===
+'''Investigator: CR, JB'''
+'''Aim of the experiment:''' MiniPrep and NanoDrop of F26 K1, K2 and K3
+Sequencing of P51
+'''Procedure:'''
+MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+Concentrations were as following:
+* P51: 163,3
+* P52: 151,7
+* P53: 140,5
+P51 was sequenced:
+* 1. with VF2: FR11326626
+* 2. with VR: FR11326625
+</div>
+<div class="polymerization">
+=== Biotinylation of eGFP ===
+'''Investigator: VL, JB'''
+'''Aim of the experiment:''' Biotinylation of eGFP with 200x biotin-NHS molar excess over eGFP (15x excess over surficial K residues). NB: previous trial unsuccessful. Excess of biotin was likely insufficient to ensure efficient biotinylation, esp. since biotin-NHS slowly hydrolyzes in the aqueous environment.
+'''Procedure:'''  1 ml of eGFP was biotinylated with an 200x excess of biotin in DMF (100 uM; 38 uL), 5.5 h at rt. The solution was dialysed versus 20 mM Tris/HCl pH 8 overnight at 4 °C.
+</div>
+<div class="general">
+=== PCR of gene syntheses ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Amplification od iGEM_1_SA-m1 (F27), iGEM_1_mRuby_EGFR (F28) and iGEM_2_IRES-BirA (F29)
+'''Procedure:'''
+* Add 100µl of ddH2O to the gene sythesis samples and incubate for 20 min at 50°C
+* Dilute samples to a final concentration of max. 1ng/µl (1:10) with water.
+* Approach:
+µl DNA (diluted)
+µl buffer
+,5µl dNTPs
+,25µl forward Primer VF2
+,25µl reverse Primer VR
+,25µl Q5 Polymerase
+Fill up with water up to 25µl
+* Make sure to pipette everything on ice and add the polymerase at the end
+* Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)
+°C_1min initiation step
+°C_10sec
+°C_30sec   >  step 2-4: 35 repeats
+°C_30sec
+°C_2min final step
+°_hold
+* The samples were then prepared with the PCR Product Purification Kit
+</div>
+<div class="polymerization">
+=== Polymerisation experiments for biotinylated eGFP and BSA with Streptavidin ===
+'''Investigator: JH, CR, JB'''
+'''Aim of the experiment:''' Determination of ideal concentrations for both protein interaction partners as well as buffer viscosity (glycerol content etc.) for polymerisation in a test tube
+'''Procedure:'''
+* Different concentrations of proteins and glycerol were tested to support stable polymerisation without protein aggregates rising to the surface or sinking to quickly
+* The experiments done are not going to be further documented as the streptavidin used for the experiments was previously determined in a wrong fashion and was actually considerably lower than expected (4x lower). Streptavidin was, due to that circumstance, concentrated to be able to support experiments with at least 5 mg/ml concentrations
+* First experiments with concentrated streptavidin seemed promising, though a complete series of experiments with varying parameters should be conducted in the future
+</div>
+<div class="general">
+=== Sequencing of P29 (pSB1C3 (double terminator), P36 (pSB1C3 (Tet repressed RFP)) and P37 (pSB1C3 (Tet repressed RFP)) ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Sequencing of P29, P36 and P37
+'''Procedure:'''  According to the manufacturer's protocol.
+* P29: FR11326624 (VF2)
+* P36: FR11326623 (VF2)
+* P37: FR11326621 (VR), FR11326622 (VF2)
+</div>
+<div class="general">
+=== Inoculation of (pre)cultures for a pSB1C3 midiprep ===
+'''Investigator: JB, VM'''
+'''Aim of the experiment:''' Massively amplifying the pSB1C3 vector (which will be needed for building up new biobricks) by midiprepping the P40 plasmid (RFP-generator in pSB1C3). Similar to minipreps, but on a greater scale.
+'''Procedure:'''  3 ml precultures were inoculated with a clone from the plate previously used for minipreps. After the precultures had grown for 4 hours (due to shortage of time), 2 x 50 ml cultures were inoculated and shaken overnight at 37°C. The next day, cultures were put into the fridge for storage until Monday.
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 5 (June 13th - June 19th)=
+<div class="week" id="Week_5">
+=='''Monday, June 13th'''==
+<div class="receptor">
+=== Digestion of gene synthesis iGEM1 and iGEM2 ===
+'''Investigator: LK, JH'''
+'''Aim of the experiment:''' Digest F28 (iGEM1) and F29 (iGEM2) in order to ligate them into P40, which was equally digested (to get rid of the rfp-generator and have pSB1C3 as backbone)
+'''Procedure:'''
+* 30µl of F28 were digested for 3h with SpeI and NgoMIV, and 30 µl of F29 were digested with XbaI and PstI
+* 2 x 20 µl where digested with the equivalent enzymes for 3h
+* After electrophoresis the bands were cut out and purified
+'''Results:''' Results show that PCR of F28, F29 might not have worked. P40 was extracted from gel (F30 and F31). PCR of gene synthesis was repeated (50µl!)
+</div>
+<div class="general">
+=== Midiprep of P40 ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Purification of P40 from
+'''Procedure:'''
+* See protocol of Midiprep kit
+* 1xuse-centrifugation-columns broke in centrifuge during last step, DNA rescue was tried by resuspending rest of the solution in the tube in EB buffer and redo the last steps (isoprop and ethanol precipitation)
+* Airdry "pellet"(no pellet visible) for 15 min under fume hood and resuspend in 100µl EB Buffer
+* Measure concentration with nanodrop
+</div>
+<div class="polymerization">
+=== Preparation of Collagen + Biotinylation ===
+'''Investigator: VL, JL'''
+'''Aim of the experiment:''' prepare collagen solution + biotinylate small sample
+'''Procedure:'''
+* Dissolve 5 g collagen in 50 mL Tris/HCl pH 8 20 mM w/o salt --> 770 uM solution (100 mg/mL)
+* Sterile filter
+* Biotinylation: 980 uL Tris buffer + 20 uL collagen solution + 30 uL biotin-NHS (100 mM in DMF, 200x molar excess over collagen monomers)
+* Reaction time:
+* Dialyze 4 °C Tris/HCl pH 8 20 mM w/o salt o/n
+</div>
+<div class="streptavidin">
+=== Transformation of P9 (pASK75) ===
+'''Investigator: JL, VL'''
+'''Aim of the experiment:''' transform streptavidin expression vector P9 (clone 4) into E. coli BL21
+'''Procedure:'''
+* Standard (see booklet): 45 s at 42 °C; incubate 1h, 37°C; plate: medium w. chloramphenicol (+ rescue plate) Incubate o/n 37°C.
+* Wrong antibiotic plate, repeated the next day of the experiment:''' Massively amplifying the pSB1C3 vector (which will be needed for building up new biobricks) by midiprepping the P40 plasmid (RFP-generator in pSB1C3). Similar to minipreps, but on a greater scale.
+</div>
+=='''Tuesday, June 14th'''==
+<div class="polymerization">
+=== Mass spectrometry of biotinylated eGFP ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' identify biotinylation degree of eGFP
+'''Procedure:'''
+ [generic_display_report] (i could not upload this file, sorry.)
+'''Results:''' about 4-5 biotins per protein. To verify the biotinylation degree the unbiotinylated eGFP will be measured.
+</div>
+<div class="receptor">
+=== Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Purification of PCR products
+'''Procedure:'''
+* Volume of PCR reaction: 50 µL
+* PCR products were purified by manufacturers protocol (QIAquick PCR purification kit, Qiagen)
+* Concentration measured by Nanodrop:
+* F32: 87,5 ng/µL
+* F33: 68,3 ng/µL
+* Test if PCR worked:
+* Samples were applied on a 2% agarose gel and was run at 80 V for 40 min.
+'''Results:'''
+[[File:Muc16_PCR_F32_F33.png|500px]]
+* PCR of F28 worked --> F32
+* PCR of F29 did not work --> wrong primers were used for amplification --> F33 not right (Re-Do PCR with appropriate primers
+</div>
+<div class="receptor">
+=== Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3 ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Digestion of F32 (SpeI, NgoMIV) and F33 (XbaI, PstI)
+'''Procedure:'''
+* Digestion F32: 27 µl of F32 (2.4 µg), 5 µl CutSmart Buffer, 1.5 µl SpeI, 2 µl NgoMIV, 14.5 µl H2O
+* Digestion F33: 27 µl of F32 (1.8 µg), 5 µl CutSmart Buffer, 1.5 µl XbaI, 1.5 µl PstI, 15 µl H2O
+* Incubation for 3 h at 37°C
+* Preperative gel:
+[[File:Muc16_PCR_F32_F33_praep-gel.png|500px]]
+* Gelextraction of F32 upper band and F32 lower band was executed by manufacturers protocol (Qiagen)
+* F32 upper band (mRuby) was named F34 (=10 g/yl)
+* F32 lower band (eGFR) was named F35 (=6 ng/yl)
+</div>
+<div class="receptor">
+=== Cloning of F32 (PCR iGEM_1 mRuby-EGFR) and F33 (PCR iGEM_2 IRES-BirA) in pSB1C3 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Ligation of F34 (mRuby) and F35 (eGFR) in F30 (pSB1C3); Tranformation in XL1blue
+'''Procedure:'''
+* Ligation mixtures were prepared as following:
+* F34: 8.0 μL F34, 2 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase)
+* F35: 7.6 μL F35, 2.4 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase)
+* Ligation was incubated for 30 min at RT
+ [something is missing here]
+</div>
+<div class="receptor">
+=== Re-Sequencing of P37 (Tet repressed YFP) ===
+'''Investigator: CG'''
+'''Aim of the experiment:'''
+Purification and sequencing of P30
+'''Procedure:'''
+* P30 was heated up to 100 °C and centrifugated afterwards to remove proteins from Promotor (if there are some), the supernatant is sequenced
+* Sequencing batches were prepared after manufacturer's protocol
+* (15 μL plasmid DNA (50-100 μM) and 2 μL sequencing primer)
+* The plasmid we prepared received the following barcode: P37 (VF2) : FR11326620
+</div>
+<div class="streptavidin">
+=== Streptavidin expression ===
+'''Investigator: CR'''
+'''Aim of the experiment:'''
+Transformation of P9 (pASK74 (SA1)) in BL21
+'''Procedure:'''
+* Transformation was executed following SOP
+* Transformed cells were plated on LB medium (Amp) (50 µL and rescue (50 µL)
+</div>
+<div class="streptavidin">
+=== Dialysis of Streptavidin and biotinylated BSA ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Streptavidin and bitinylated BSA are both in Tris/HCl without salt. SInce we will perform later experiments in salty solutions the dialysis was performed against 137 mM NaCl (Saltconcetration of PBS)
+'''Procedure:'''
+* 3 L Tris/HCl NaCl solution was prepared
+* Dialysis was prepared according to SOP
+* Cut off Dialysis hose: 14 kDa
+</div>
+<div class="general">
+=== Inoculation of (pre)cultures of P40 for a pSB1C3 midiprep [repeat] ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Massively amplifying the pSB1C3 vector by midiprepping the P40 plasmid (RFP-generator in pSB1C3)
+'''Procedure:'''  four 4 ml precultures were inoculated with a clone from the plate previously used for minipreps. After the precultures had grown for 6 hours, 50 ml cultures were inoculated and shaken overnight at 37°C.
+</div>
+<div class="receptor">
+=== Subcloning of P41 (strong RBS-p(cat)) Insert into pSB1C3 ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Moving P41 (pSB1A2; Pcat+weakRBS) to pSB1C3 for biobrick submission
+'''Procedure:'''
+* Digestion of P41 with XbaI and PstI (10 µl DNA, 1,5 µl each enzyme, 3 µl CutSmart buffer x10, 14 µl ddH2O) -> Incubation at 37°C for 2h.
+* Electrophoresis: 2% Agar, 40 min , 90 V (1kb ladder, empty, P41, 100b ladder)
+* GelExtraction
+'''Resuts:''' no visible signal of insert at approx. 100b. Area was cut blind for GelEx. No DNA in the sample according to NanoDrop measurement. Repeated the next day.
+</div>
+<div class="receptor">
+=== Inoculation of colonies from NanoLuc ===
+'''Investigator: JH'''
+'''Procedure:'''
+* 2x 4 ml LB+Cam media
+* Each culture was inoculated with one colony
+*Incubation at 37°C overnight
+</div>
+=='''Wednesday, June 15th'''==
+<div class="receptor">
+=== Subcloning of P41 (strong RBS-p(cat)) Insert into pSB1C3 ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Moving P41 (pSB1A2; Pcat+weakRBS) to pSB1C3 for biobrick submission. No gel extraction was performed because the fragement is too small to visualize on the gel.
+'''Procedure:'''
+* Digestion of P41 with XbaI and PstI (10 µl DNA, 1,5 µl each enzyme, 3 µl CutSmart buffer x10, 1 µl FastAP, 13 µl ddH2O) -> Incubation at 37°C for 2 h, heat inactivation at 80°C for 20 min.
+fragement is to small to visualize on agel.
+* Subcloning into F31: 3.8 μL F38, 6.2 μL F31, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase according to the SOP
+* Transformation into E. coli XL1 according to the SOP
+</div>
+<div class="receptor">
+=== Miniprep of pSB1C3(Nanoluc)  ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Preperation of a BioBrick with NanoLuciferase in pSB1C3
+'''Procedure:'''
+*The Miniprep was done according to the protocol.
+*The two tubes where pooled.
+*The new Plasmid is found under P54 and was sent to sequencing.
+</div>
+<div class="polymerization">
+=== Polymerisation ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Determine optimal polymerisation conditions for BSA and Collagen
+'''Procedure:''' The experiment was performed in a 96 Well plate:
+[[File:Muc16_excel_table.png|500px]]
+[[File:Muc16_well_plate.png|500px]]
+'''Results:''' maximum concentration of Streptavidin and biotinylated Protein works best. Collagen does not work. Glycerolconcentrations do not inhibit interaction. Reaction might be to slow at given concentrations to be effective in printing process.
+</div>
+<div class="general">
+=== MidiPrep of pSB1C3 with RFP generator (P4) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' purification of pSB1C3 with RFP generator for further processing (P56)
+'''Procedure:'''
+*MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)
+'''Results:'''
+Concentration very low (12ng/μL), but high volume (500 μL)
+</div>
+=='''Thursday, June 16th'''==
+<div class="receptor">
+=== MiniPrep of F36 (Ligation mRuby in pSB1C3) K1 & K2, F37 (Ligation EGFR in pSB1C3), I13453 (pBad promotor) K1 & K2, K577881 (pC+AraC+pBad+GFPc) K1 & K2 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' isolate Plasmids
+'''Procedure:'''
+* MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Plasmids were named as following: [concentration]
+F36 K1: P57 [212,9 ng/μL]
+F36 K2: P58 [181,3 ng/μL]
+F37: P59 [195,5 ng/μL]
+K577881 K1: P60 [557,2 ng/μL]
+K577881 K2: P61 [791,9 ng/μL]
+I13453 K1: P62 [130 ng/μL]
+I13453 K2: P63 [460 ng/μL]
+</div>
+<div class="general">
+=== Sequencing of P29 (double terminator), P36 (Tet repressed RFP) and P37 (Tet repressed YFP)===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Sequencing of P56, P57, P59, P61 and P62
+'''Procedure:'''  According to the manufacturer's protocol.
+* P56: FR11326618 (VF2)
+* P57: FR11326617 (VF2)
+* P59: FR11326616 (VF2)
+* P61: FR11326613 (VR), FR11326615 (VF2)
+* P63: FR11326614 (VF2)
+</div>
+<div class="general">
+=== MidiPrep P4 (pSB1C3) ===
+'''Investigator: VL'''
+'''Aim of the experiment:''' isolate Plasmids
+'''Procedure:'''
+* MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen). Centrifugation steps at 20,000 g performed at 12,500 rpm in special centrifugation tubes. Since only one column was left, both prepped cell pellets were applied to one column. Flow-through and wash was collected.
+* Conc:
+</div>
+<div class="general">
+=== Amplification of BioBricks (overnight cultures for minipreps) ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Inoculation of 5 ml overnight cultures for minipreps. The following biobricks were used:
+* BBa_K157012
+* BBa_K243004
+* BBa_K243006
+* BBa_K157001
+* BBa_K243005
+* BBa_I712009
+* BBa_K404108
+* BBa_K782061
+* BBa_K1371012
+* BBa_K782060
+'''Procedure:'''
+* Three hours of incubation of the tubes containing the bacterial agar at 37°C (Note: 12 hours are actually recommende)
+* Inoculation of two times 5 ml preculture containing the appropriate antibiotic per clone. For KanRAmpR (reistance against both ampicillin and kanamycin) it was only selected for ampicillin.
+* Incubation shaking overnight at 37°C
+</div>
+<div class="receptor">
+=== PCR Amplification of genesynthesis 2 (F29; IRES-BirA) ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Amplification of Genesynthesis_2 (IHRES_BirA_StrepTag)
+'''Procedure:''' A 50µl approach was made:
+* 33,5 µl Water
+* 2µl DNA (F29, diluted 1:10)
+* 2,5µl of each Primer (O11 and O12 c:10µM)
+* 0,5µl dNTPmix
+* 5µl Reaction buffer
+* 0,5µl Q5-Polymerase
+* The Annealing Temp. was set an 58°C
+* Next step is to run an analytic gel (band should be visible at 1,5 kB)
+</div>
+=='''Friday, June 17th'''==
+<div class="receptor">
+=== Cloning of genesynthesis 2 (IRES-BirA) into pSB1C3 ===
+'''Investigator: CG, NA, JH'''
+'''Aim of the experiment:''' Purification oft he PCR reaction, gel verification, restriction digestion (F29), ligation with F31 and transformation
+'''Procedure:'''
+* Yesterdays PCR was purified according to Qiagen PCR purification kit
+* An anlaytic gel electrophoresis was performed on a 1% gel with 4 µl purified PCR product
+* Restriction digest: 26 µl purified PCR product, 1.5 µl XbaI, 1.5 µl PstI, 5 µl NEB SmartCut, 16 µl H2O. Incubation for 2 h at 37°C.
+* Gel extraction
+* Ligation: F31
+* Transformation
+'''Results:''' Gel electrophoresis after PCR purification exhibit a thin signal at 1.5 kb. Next time 1:30 min for elongation time might increase the signal.
+[[File:Cloning_of_gene_synthesis_2_into_pSB1C3.png|200px]]
+ </div>
+ <div class="general">
+=== Miniprep new iGEM BioBricks ===
+'''Investigator: VL'''
+'''Aim of the experiment:''' Purify plasmid DNA from transformed cells
+'''Procedure:'''
+* Miniprep according to manual (pellet centrifuged 5000 rpm, 10 min, 4 °C)
+* Elution with 50 uL EB Buffer
+* Concentrations (all ng/uL):
+K782061 (a) 172.9, (b) 53.0
+K243006 (a) 241.1, (b) 58.6
+K1371012 (a) 138.0, (b) 43.0
+K157001 (a) 184.3, (b) 186.4
+K782060 (a) 339.0, (b) 254.0
+K243005 (a) 62.3, (b) 176.2
+K243004 (a) 122.3, (b) 110.3
+I711009 (a) 185.2, (b) 174.7
+K157012 (a) 181.2, (b) 195.3
+K404108 (a) 116.4, (b) 142.5
+</div>
+<div class="general">
+=== MidiPrep of pSB1C3 with RFP generator (P4) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' purification of pSB1C3 with RFP-Reportercasette for further processing (P74)
+'''Procedure:'''
+MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)
+'''Results:'''
+</div>
+<div class="receptor">
+=== Cloning of IRES-BirA (F33->F40) into digested F31 (pSB1C3) ===
+'''Investigator: JH, LK'''
+'''Aim of the experiment:''' Ligation of IRES-BirA (F29->F33->F40) into F31 (digested P40 by XbaI and PstI = pSB1C3 without insert), gelelectrophoresis and tranformation in XL1blue
+'''Procedure:'''
+* F33 (PCR product of F29/gen synthesis 2) was digested with XbaI and PstI
+* Gelextraction of band at 1500 bp was executed by manufacturers protocol (Qiagen)
+* intermediate result: F40 with 6.6 ng/µL
+* Ligation mixtures were prepared as following:
+* 9.6 µL F40, 0.4 µL F31, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* Transformation: (Saturday)
+* Transformation of Ligation (F29+F31) into XL-1 blue was done according to the SOP. The plate was incubated until Sunday at 37°C.
+* 3mL-cultures in LB+ 30µg/ml cam where inoculated on Sunday
+* Mini-prep according to manufacturer's protocol was done on Monday.
+</div>
+<div class="receptor">
+=== PCR, purification and digestion of P19 (EspP) and F28 (mRuby EGFR) for BioBrick creation ===
+'''Investigator: JB, LK'''
+'''Aim of the experiment:''' Amplification of EspP from P19 and mRuby/EGFR (F28) for creation of Biobricks
+'''Procedure (for both fragments):'''
+* PCR according to the SOP (primers for P19: O13 and O03, primers for F28: VR and VF2)
+* PCR purification via the purification kit according to the manufacturer's protocol (concentrations: P19(EspP):119,5 ng/µl F28(mRuby):56,2ng/µl
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+* Restriction digestion with NgoMIV/SpeI (for both cases)
+* 40µl DNA
+* 1,5µl of each Enzyme
+* 2µl ddH2O
+* 5µl CutSmart Buffer
+* The tubes where incubated at 37°C for ~2 days.
+'''Results:'''
+Analytical gel electrophoresis after PCR purification shows thick bands at roughly 1000 bp
+'''Still to do:'''
+* Gel extraction of both signals for F28 and one signal for EspP-PCR
+* Ligation with appropriate vector (e.g. F30)
+* Transformation
+</div>
+<div class="general">
+=== Minipreps of F39 (strong RBS-pcat in pSB1C3) ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Amplification of F39 (ligation, pCat with strong RBS)
+'''Procedure:'''
+* Miniprep according to the manufacturer's protocol
+* Resulting plasmid: P76
+* Concentration: 52 ng/µl
+</div>
+<div class="general">
+=== Minipreps of pSB1C3 with RFP generator (P4) ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' purification of pSB1C3 with RFP-Reportercasette for further processing (P75)
+'''Procedure:'''
+* Minipreps according to the manufacturer's protocol (with 8* 6 mL culture)
+* Resulting plasmid: P75
+* Concentration: 142.2 ng/µl [~200 µL]
+</div>
+<div class="receptor">
+=== Inoculation of colony from NanoLuc [P54, Repeat] ===
+'''Investigator: JH'''
+'''Procedure:'''
+* 5 ml LB+Cam media
+* culture was inoculated with one colony
+* Incubation at 37°C overnight
+</div>
+=='''Saturday, June 18th'''==
+<div class="receptor">
+=== Miniprep of P54 (NanoLuc) ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Purification of P54 (NanoLuc)
+'''Procedure:'''
+* Miniprep according to the manufacturer's protocol
+* Resulting plasmid: pSB1C3 mit NanoLuc (P54, von )
+* Concentration: 497,9 ng/µl
+</div>
+<div class="receptor">
+=== Hybridisation of O19 and O20 (StrepTag) ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Hybridisation of the Strep-Oligos
+'''Procedure:'''
+µl of each Oligo where diluted in 16µl ddH2O and incubated for 10 min. at 95°. Cooling down at RT for at least half an hour. Stored in fridge
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 6 (June 20th - June 26th)=
+<div class="week" id="Week_6">
+=='''Monday, June 20th'''==
+<div class="receptor">
+=== Miniprep of F42 (IRES-BirA in pSB1C3) ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Purification of IRES-BirA Plasmids
+'''Procedure:'''
+* Miniprep according to the manufacturer's protocol
+* Resulting plasmid: pSB1C3 with IRES-BirA
+Next Steps:
+* analytical digestion with EcoRI+PstI and gel (expected bands at 1500 and 2000 Bp)
+* Sequencing
+'''Results:'''
+Concentration: 583,5 ng/µl
+</div>
+<div class="receptor">
+=== PCR and Purification of BirA ===
+'''Investigator: LK, JB'''
+'''Aim of the experiment:''' Amplification of BirA-construct
+'''Procedure:'''
+* PCR according to the SOP (primers: O17 and O18)
+* PCR purification via the purification kit according to the manufacturer's protocol
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+'''Results:'''
+* Concentration: 185,8 ng/µl --> F41
+* Analytical gel shows no significant band at 960 Bp -->Repeat
+Next Steps:
+* Repetition of PCR and analytical gel!
+</div>
+<div class="receptor">
+=== Gel and Gelextraction of P19 (QC EspP) and F28 (EspP and mRuby) ===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Purification of both constructs for Ligation
+'''Procedure:'''
+* Preperative gel according to SOP
+* The Purification was done according to the manufacturer's protocol. The EGFR gel-fragment was eluted in 50µl and the mRuby-fragment in 30µl (because of thin band)
+'''Results:'''
+* One thick band just before 1000Bp and one lighter band just before 750 Bp. This fits to the lengths of EspP and mRuby.
+* Concentrations: EspP(now F43): 49,5ng/µl   mRuby(now F44): 9,9ng/µl
+Next Steps:
+* Ligation into pSB1C3
+</div>
+<div class="general">
+=== Sequencing of F42 (pSB1C3(IRES-BirA)), P54 (pSB1C3(NanoLuc)) , P74 (pSB1C3(RFP generator)) and P76 (pSB1C3(strong RBS-pCat))===
+'''Investigator: JL'''
+'''Aim of the experiment:''' Sequencing of F42, P54, P74 and P76 in forward direction.
+'''Procedure:'''
+Sequencing batches were prepared after manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+The different plasmids we prepared received the following barcodes:
+* F42 (VF2): FR11326601
+* P54 (VF2): FR11326600
+* P74 (VF2): FR11326599
+* P76 (VF2): FR11326598
+</div>
+<div class="streptavidin">
+=== PCR and Purification of genesynthesis 6 (iGEM6) Streptavidin/Traptactin ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Amplification of gen synthesis 6
+'''Procedure:'''
+PCR according to the SOP (primers: VF2 and VR)
+Next Steps:
+* PCR purification via the purification kit according to the manufacturer's protocol
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+* PCR purification via the purification kit according to the manufacturer's protocol
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+</div>
+<div class="receptor">
+=== PCR and Purification of BirA (F41) ===
+'''Investigator: NA '''
+'''Aim of the experiment:''' Amplification of BirA (F29)
+'''Procedure:'''
+PCR according to the SOP (primers: O17 and O18)
+Next Steps:
+* PCR purification via the purification kit according to the manufacturer's protocol
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+* PCR purification via the purification kit according to the manufacturer's protocol
+* Analysis on an 1% agarose gel using 5 µl purified PCR product
+--> repeat with gene-synthesis 2 (F29 may not be the gene-synthesis 2)
+</div>
+<div class="receptor">
+=== Ligations of StrepTag, EspP and mRuby3 with F30 (digested pSB1C3) ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Ligations of StrepTag (O19+O20), EspP (F43) and mRuby3 (F44) into F30 (NgoMIV and SpeI; pSB1C3 without insert)
+'''Procedure:'''
+* Ligation mixtures were prepared as following:
+* O19+O20: 1.7 (O19+O20), 8.3 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* F43: 	4.6 μL F43, 5.4 µL F30, 2 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* F44: 	8.1 μL F44, 1.9 μL F30, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* Ligation was incubated overnight at 16 °C
+</div>
+<div class="streptavidin">
+=== Digestion of GSY5 (Streptactin; F27)===
+'''Investigator: LK'''
+'''Aim of the experiment:''' Restricting GSY5 into StrepActin fragment (Streptavidin mutant) and Leptin fragment (Leptin is for Volker)
+'''Procedure:'''
+* Restriction mix:
+µl DNA (F27)
+µl ddH2O
+µl of each enzyme (SpeI, HindIII, SapI)
+µl cut smart buffer
+Next Steps:
+* Preperative gel, 1,5% Agarose, cut out and purify bands at 80 Bp and 425 Bp. (80 is leptin for volker and 425 is StreptActin for further cloning into pASK)
+'''Results:'''
+</div>
+=='''Tuesday, June 21st'''==
+<div class="general">
+=== Plating of BioBricks that didn't survive sequencing ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Instead of directly inoculating cultures with the transformed cells from the bacterial agar that was sent by the HQ, the bacterial agar was now used for overnight plating on agar plates containing the appropriate antibiotic resistance.
+'''Procedure:''' Two methods were used for each BioBrick: For the first method, an inoculation loop was used for plating directly. For the second methods, the inoculation loop was used to inoculate a 50 µl LB culture that
+</div>
+<div class="general">
+===Sequencing of various plasmids ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Sequencing of various plasmids with either VF2 or VR
+'''Procedure:'''
+Refer to the “Inventarliste” for detailed informations on sequencing codes and primers. Sequencing batches were prepared according to manufacturer's protocol (15 µL plasmid DNA (50-100 µM) and 2 µL sequencing primer)
+</div>
+<div class="receptor">
+=== PCR of gene synthesises (iGEM_1) (mRuby_EGFR) ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' iGEM_1_mRuby_EGFR (F28) for preparing the EGFR signal (at about 100 bp)
+'''Procedure:'''
+Approach:
+* 1µl DNA (diluted, 1:10)
+* 25 µl 2x MasterMix
+* 0,5µl dNTPs
+* 2,5 µl forward Primer VF2
+*2,5µl reverse Primer VR
+* Fill up with water up to 50 µl
+Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)
+* 98°C_1min initiation step
+* 98°C_10sec
+* 66°C_30sec   >  step 2-4: 35 repeats
+* 72°C_30sec
+* 72°C_2min final step
+* 4°_hold
+</div>
+<div class="receptor">
+=== Transformation of Ligations of F50 (StrepTag), F51 (EspP) and F52 (mRuby3) in pSB1C3 ===
+'''Investigator: JH'''
+'''Aim of the experiment:''' Transformation of StrepTag (F50), EspP (F51) and mRuby3 (F52) in XL1 blue
+'''Procedure:'''
+transformation in competent E. Coli XL1 blue according to protocol + rescue
+(repeat due to incubation with LB+Cam ! )
+'''Result:'''
+plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+<div class="receptor">
+=== Digestion of P9 (pASK75), P74 (pSB1C3), P26 (CMV promotor) and F47 (BirA) ===
+'''Investigator: JB'''
+'''Aim of the experiment:''' Digestion of P9 and P74 to gain the vectors pASK75 and pSB1C3, respectively, as well as digestion of F47 (PCR fragment of BirA) and P26 (CMV promoter) for the ultimate creation of biobricks
+'''Procedure:''' P74 was digested in a total volume of 30 µl, while the others were digested in a total volume of 50 µl. Enzymes used were:
+* P74: XbaI and PstI
+* P9: HindIII and XbaI
+* F47: Xba I and PstI (didn’t work)
+* P26: SpeI and PstI
+The digestions were incubated at 37°C for 40 minutes and were thereafter inactivated at 80°C for 5 mins.
+</div>
+<div class="receptor">
+=== Inoculation of cultures for minipreps for P76 (pCat + strong RBS) ===
+'''Investigator: JB'''
+'''Procedure:''' Inoculation of 2x5 ml cultures with P76 clones. Incubation at 37°C overnight.
+</div>
+=='''Wednesday, June 22nd'''==
+<div class="receptor">
+=== Minipreps of P79 (pCat+RBS) ===
+'''Investigator: JB'''
+'''Procedure:''' According to the manufacturer's protocol.
+'''Results:''' Concentration 212 ng/µl. Sent to sequencing
+</div>
+<div class="general">
+=== Transformation of ligation F56 (pASK75(Streptactin)), P60 (pSB1C3 (pC+AraC+pBad+GFPc)) , P70 (pSB1C3 (short linker)) ===
+'''Investigator: CG'''
+''Aim of the experiment:''' Transformation of pASK75-Streptactin (F56) into E.&nbsp;''coli'' XL1 blue, K577881 (P60) into BL21 and K243004 (P70) in XL1
+'''Procedure:'''
+transformation in competent E. Coli XL1 blue according to protocol
+'''Result:'''
+plates (LB + appropriate antibiotic) in incubator for further processing (37 °C)
+</div>
+<div class="receptor">
+=== Inoculation of colonies from K157001 (EGFR signal peptide), EspP (F50), mRuby (F51), Strep-Tag (F52) ===
+'''Investigator: CG'''
+'''Procedure:'''
+* 2x 5 ml LB+Cam (Amp for K157001)  media
+* Each culture was inoculated with one colony, for ligations 2 colonies each
+* Incubation at 37°C overnight
+</div>
+<div class="receptor">
+=== Plateing of K243004 (short linker), K243005 (middle linker) from stab cultures ===
+'''Investigator: CG'''
+'''Procedure:'''
+For both biobricks: stabing into the agar with the inocluation loop and resuspending in 50 µl LB media. Plating on Amp-agar.
+</div>
+<div class="receptor">
+=== Digestion of P64 (EGFR sgnal peptide) and P71 (CD4 signal peptide) for cloning into F57 (pSB1C3 (CMV promotor)) ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Digestion of P67 and P71 for cloning the resulting fragments into the digested F57 fragement.
+'''Procedure:''' both plasmids were digested in 50 µl, 3 µg for each plasmid DNA. 1 µl of XbaI and PstI, 5 µl Buffer, 20 µl DNA, 23 µl H2O. The digestions were incubated at 37°C overnight.
+</div>
+<div class="receptor">
+=== Preparative agarose gels for separation of digestion of P64 (EGFR sgnal peptide) and P71 (CD4 signal peptide) ===
+'''Investigators: NA, JB'''
+'''Aim of the experiment:''' Separation of digestion fragments of both digested PCR fragments as well as vectors
+'''Procedure:'''
+* P74: XbaI and PstI -> Fragment corresponding to the pSB1C3 vector isolated
+* P9: HindIII and XbaI -> Fragment corresponding to the pASK75 vector isolated
+* F47: Xba I and PstI (didn’t work) –> only one fragment at 3 kbp present (weird since that was a gene synthesis pcr)
+* P26: SpeI and PstI  -> Fragment corresponding to the cmv-promoter isolated
+[[File:Muc16_praep_p74_p9.png|500px]]
+[[File:Muc16_praep_p26.png|500px]]
+* Gelextraction of P9, P74 and P26 was executed by manufacturers protocol (Qiagen)
+'''Results:'''
+* F55: pASK75 (2,9 ng/µl)
+* F56: pSB1C3 (23,6 ng/µl)
+* F57: CMV-Promotor (5,9 ng/µl)
+</div>
+<div class="receptor">
+=== PCR of GSY2 (IRES-BirA) with O17/18 ===
+'''Investigators: LK'''
+'''Aim of the experiment:''' Amplification of BirA, using new dilution of GSY2 this time, because last 2 PCRs showed confusing results (bands at 2500)
+'''Procedure:'''
+* PCR was performed  according SOP
+* Primers: O17 and O18
+* Annealing at 68°C
+Next Steps:
+* PCR-Purification
+* Analytical Gel
+* Ligation into pSB1C3
+</div>
+<div class="streptavidin">
+=== QuickChange-PCR of pASK75 with O21 and O22 ===
+'''Investigators: LK'''
+'''Aim of the experiment:''' Deleting NdeI from pASK (P03)
+'''Procedure:'''
+* QC-PCR was performed according to SOP
+* Primers: O-021 and O-022
+* Annealing at 68°C
+* Elongation time: 3:30 min
+Next Steps:
+* Digestion with DpnI at 37°C for 1h
+* Purification?
+* Preperative Gel (band at 960), purification
+* Ligation into pSB1C3
+</div>
+<div class="receptor">
+=== Verification of PCR and Digestion of F28 (gene synthesis 1) ===
+'''Investigator: NA, LK'''
+'''Aim of the experiment:''' Verification of successful PCR via gel electrophoresis and preparation of EGFR
+'''Procedure:'''
+* Gel electrophoresis with 1 kb-ladder
+* Digestion: 42µl of PCR Purification, 1,5 µl of each enzyme (NgoMIV and SpeI), 5µl of cut smart buffer.
+* Incubation at 37°C over night
+'''Results:'''
+[[File:Muc16_analytic_after_pcr_F28.png|500px]]
+Next steps:
+* Preparative gel and gel extraction
+* Ligation into pSB1C3
+</div>
+=='''Thursday, June 23th'''==
+<div class="receptor">
 ===Miniprep of E. coli Xl1-Blue transformed with ligation product P80/81 (mRuby3 K1/2), P82/83 (EspP K1/2), P84/85 (StrepTag K1/2) and Trafo of K157001===
@@ Line 421: / Line 2,969: @@
 '''Aim of the experiment:''' Miniprep of E. coli Xl1-Blue transformed with ligation product F50(K1,2), F51(K1,2), F52(K1,2) and Trafo of K157001
 '''Procedure:'''
 * Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
 * Concentrations:
-<table cellspacing="0" border="1">
+<table class="wikitable" cellspacing="0" border="1">
 <tr>
 <td><b>Plasmid</b>
@@ Line 459: / Line 3,008: @@
 </div>
-<div class="Receptor">
+<div class="receptor">
+=== PCR of gene synthesises ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' iGEM_1_mRuby_EGFR (F28) for preparing the EGFR signal (at about 100 bp)
+'''Procedure:'''
+Approach:
+* 1µl DNA (diluted, 1:10)
+* 25 µl 2x MasterMix
+* 0,5µl dNTPs
+* 2,5 µl forward Primer VF2
+* 2,5µl reverse Primer VR
+* Fill up with water up to 50 µl
+Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)
+* 98°C_1min initiation step
+* 98°C_10sec
+* 66°C_30sec   >  step 2-4: 35 repeats
+* 72°C_30sec
+* 72°C_2min final step
+* 4°_hold
+</div>
+<div class="streptavidin">
+=== QuickChange-PCR of pASK with O21 and O22 ===
+'''Investigators: CR'''
+'''Aim of the experiment:''' Digestion of PCR product with DpnI to digest methylated DNA
+'''Procedure:'''
+</div>
+<div class="receptor">
+=== PCR purification of BirA and mRuby/EGFR ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' purification of PCR
+'''Procedure:'''
+PCR purification via the purification kit according to the manufacturer's protocol
+The samples were renamed:
+* BirA: F59
+* mRuby/EGFP: F60
+The samples were analysed on a 1% agarose gel. Samples were prepared after SOP.
+'''Results:'''
+[[File:Muc16_pcr_F59_F60.png|500px]]
+</div>
+<div class="general">
+=== Transformation of P60 (K577881; pC+AraC+pBad+GFPc K1) and QC P3 (pASK75(SA1)) ===
+'''Investigator: EF, JB'''
+'''Aim of the experiment:''' Transformation of Q CP3 in XL1 blue; transformation of p60  in BL21
+'''Procedure:'''
+transformation in competent E. Coli BL21 and XL1blue according to protocol
+µl p60 in BL21
+µl Q CP3 in XL1 blue
+'''Result:''' plates (+ rescue plates) incubating
+</div>
+<div class="general">
+=== Cloning of CD4- and EGFR-signal peptide into pSB1C3-CMV ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Digestion of P71 and P69
+'''Procedure:'''
+* Digestions were prepared as following:
+* 20 µl CD4 (P71); 1 µl XbaI; 1 µl PstI; 5 µl CutSmart; 23 µl ddH2O
+* 7 µl pSB1C3-CMV; P26; 1 µl PstI; 1 µl SpeI; 2 µl CutSmart;  µl ddH2O
+* 20 µl EGFR-signal peptide (P67);1 µl XbaI; 1 µl PstI; 5 µl CutSmart; 23 µl ddH2O
+* Digestions were incubated for 3 h at 37 °C
+* The Samples CD4- and EGFR-signal peptide were applied to a 2% and the pSB1C3-CMV to a 1% agarose Gel
+'''Results:'''
+[[File:Muc16_Cloning_of_CD4-and_EGFR-signal_peptide_into_pSB1C3-CMV_1.png|500px]]
+--> passt
+[[File:Muc16_Cloning_of_CD4-and_EGFR-signal_peptide_into_pSB1C3-CMV_2.png|500px]]
+--> passt
+Next steps:
+* Ligation of
+</div>
+<div class="receptor">
+=== Cloning of EGFR (F62) / CD4 (F61) signale peptide into pSB1C3-CMV (F63) ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Gelextraction and ligation of EGFR- and CD4-signal peptide into pSB1C3 and transformation
+'''Procedure:'''
+* Gel extraction according to manufacturers protocol (Qiagen): F61 (CD4) 2 ng/µl, F62 (EGFR) 0.6 ng/ µl, F63 (CMV): 45 ng/ µl
+* Ligation: 1 µl T4 Ligase, 2 µl Ligase buffer, 7 µl H20, 1.8 µl vector and 8.2 µl EGFR insert or 4.3 µl vector and 5.7 µl CD4 insert
+* Transformation according to SOP
+* Plating on LB-Cam agar
+</div>
 =='''Friday, June 24th'''==
-<div class="Receptor">
+<div class="receptor">
 === Analytical digestion and gelelectrophoresis of P83 (EspP K2) and P83 (StrepTag K2) ===
@@ Line 496: / Line 3,156: @@
 [[File:Muc16_P82-85_EcoRI.png|500px]]
+[[File:Muc16_P82-85_EcoR.png|500px]]
 </div>
-<div class="Receptor">
+<div class="receptor">
-=== Sequencing of P80(mRuby3 K1), P83 (EspP K2) and P85 (StrepTag K2)===
+=== Sequencing of P80( mRuby3 K1), P83 (EspP K2) and P85 (StrepTag K2)===
 '''Investigator: Julian'''
@@ Line 521: / Line 3,182: @@
 </div>
-<div class="Receptor">
+<div class="streptavidin">
 ===  Transformation of ''E.&nbsp;coli'' XL1 blue with F64 (quickchanged P3(pSAm1)) ===
@@ Line 532: / Line 3,194: @@
 * CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
-* 10&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 1&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
 * 30&nbsp;min incubation on ice
@@ Line 538: / Line 3,200: @@
 * 5&nbsp;min. heat shock at 37&nbsp;°C
-* Adding of 750&nbsp;µl LB-medium to each tube.
+* Adding of 950&nbsp;µl LB-medium to each tube.
-* The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the cell-culture shaker.
+* The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C.
---> Quickchange did not work, do again, than new transformation!
+</div>
-<div class="Receptor">
+<div class="receptor">
 ===  Gelextraction of F67(BirA), F68(mRuby), F69(EGFR-TMD), F70(pSB1C3) and F71(pSB1C3) ===
@@ Line 554: / Line 3,216: @@
 '''Procedure:'''
 Gelextraction was performed by manufacturers protocol (Qiagen).
+</div>
+<div class="general">
+=== Cloning of F59 (BirA) and F60 (EGFR-TMD) into pSB1C3 ===
+'''Investigator: CR'''
+'''Aim of the experiment:''' Generate biobricks with EGFR-TMD and BirA
+'''Procedure:'''
+* Digestions were prepared as following:
+* 1. xµl F59 (BirA); 1 µl EcoRI; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
+* 2. 2 µl P74 (pSB1C3 (RFP-generator); 1 µl NgoMIV; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
+* 3.  xµl F60 (mRuby/EGFR); 1 µl NgoMIV; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
+* 4. 2 µl P74 (pSB1C3 (RFP-generator), 1 µl EcoRI; 1 µl SpeI; 3 µl CutSmart; 23 µl ddH2O
+* Digestion was incubated for 3 h at 37 °C
+To Do:
+* Gel (already prepared)
+* Gelextraction
+* Ligation
+* Trafo
+'''Results:'''
+[[File:Muc16_Cloning_of_BirA_and_EGFR-TMD_into_pSB1C3.png|500px]]
+. band: P74(NgoMiV, SpeI) 2. band: P74 (EcoRI, SpeI)
+[[File:Muc16_Cloning_of_BirA_and_EGFR-TMD_into_pSB1C3_2.png|500px]]
+. band: F59 	2. band: F60
+</div>
+<div class="general">
+=== Transformation of EGFR-TMD-pSB1C3 and BirA-pSB1C3 ligations ===
+'''Investigator: JB'''
+'''Procedure:''' According to protocol. Plates were incubated overnight at 37°C.
+</div>
+<div class="general">
+=== Chemical biotinylation of BSA ===
+'''Investigator: MT, JB'''
+'''Procedure:'''
+BSA was chemically biotinylated with a 20x, 40x and 60x molar excess in two different buffers:100 mM Bicin (pH 8.85) and 100 mM borate (pH 8.85) with 50 mM NaCl respectively.
+-> A total of six different tubes.
+After one hour incubation at RT, the samples were put in the freezer
+</div>
+<div class="general">
+=== Inoculation of liquid cultures (F65 and F66) ===
+'''Investigator: JB'''
+'''Procedure:'''
+* Clones were picked for inoculation of 5 ml liquid cultures containing the appropriate antibiotic
+* Incubation overnight at 37°C/shaking
+</div>
 =='''Saturday, June 25th'''==
+<div class="receptor">
 ===Miniprep of E. coli Xl1-Blue transformed with P60 (mRuby/EGFR),F58 (Ligation pASK75 + Streptactin), F65 (CMV + CD4), F66 (CMV + EGFR), P70 (Short Linker)===
@@ Line 592: / Line 3,317: @@
 </div>
-=== Analytical digestion and gelelectrophoresis of F64 (quickchanged P3) for verification of succesful quickchange ===
+<div class="streptavidin">
+=== Analytical digestion and gelelectrophoresis of F64 (quickchanged P3, pASK75(SA1)) for verification of success of quickchange ===
 '''Investigator: Niklas'''
@@ Line 606: / Line 3,333: @@
 '''Results:'''
-Photo on Monday. Just a band showing a few bp (Primer), there is no plasmid band -> Quickchange did not work
+[[File:Muc16_Quickchange_NA.JPG]]
+Just a band showing a few bp (Primer), there is no plasmid band -> Quickchange did not work
+</div>
+<div class="receptor">
-=== Inoculation of colonies from Ligation of F69 + F70 (EGFR-TMD in pSB1C3)and F44 + F30 (mRuby in pSB1C3) ===
+=== Inoculation of colonies from Ligation of F69 + F70 (EGFR-TMD in pSB1C3) and F44 + F33 (mRuby in pSB1C3) ===
 '''Investigator: Niklas'''
@@ Line 624: / Line 3,356: @@
 =='''Sunday, June 26th'''==
-<div class="Receptor">
+<div class="receptor">
 ===Miniprep of E. coli Xl1-Blue transformed with ligation product F44 + F30 (mRuby3 in pSB1C3), F66 + F70 (CMV+EGFR in pSB1C3) ===
@@ Line 651: / Line 3,383: @@
 </div>
-<div class="Receptor">
+<div class="streptavidin">
 === Repetition of Quick-Change PCR of P3 (pASK + SAm1) ===
@@ Line 663: / Line 3,395: @@
 * Reaction Mix:
 <table cellspacing="0" border="1">
+<tr>
+<td><b>volume</b>
+</td><td><b>reagent</b>
+</td></tr>
 <tr>
 <td>1,25 µl
@@ Line 668: / Line 3,404: @@
 </td></tr>
 <tr>
-<td>1,25µl
+<td>1,25 µl
 </td><td>Primer O22
 <tr>
-<td>1µl
+<td>1 µl
 </td><td> dNTP-mix
 </td></tr>
 <tr>
-<td> 5µl
+<td> 5 µl
 </td><td>Pfu-Ultra-II reaction buffer
 <tr>
-<td>1µl
+<td>1 µl
 </td><td> template DNA (1:10 dilution of p3)
 </td></tr>
 <tr>
-<td> 0,5µl
+<td> 0,5 µl
 </td><td>Pfu-Ultra-II Polymerase
 <tr>
-<td>40,5µl
+<td>40,5 µl
 </td><td> ddH2O
 </td></tr></table>
 * digestion of PCR-Product with DpnI for 1h at 37°C
+* now labeled P94
 </div>
+<div class="streptavidin">
+===  Transformation of ''E.&nbsp;coli'' XL1 blue with P94 (quickchanged P3(pSAm1)) ===
+'''Investigator: Luisa'''
+'''Aim of the experiment:''' Transformation of ''E.&nbsp;coli'' XL1 blue.
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 10&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cell suspension was plated on ampicillin plates (inclusive rescue plate) for pASK (F72) and on chloramphenicol plates for P92 and P93 and incubated over night at 37&nbsp;°C in the incubator.
+</div>
+<div class="receptor">
+=== Analytical digestion and gelelectrophoresis of P92 (mRuby), P93 (CMV + EGFR) and P94 (pASK75)  ===
+'''Investigator: Luisa'''
+'''Aim of the experiment:''' Analytical digestion and gelelectrophoresis of P92 (mRuby), P93 (CMV + EGFR) and P94 (pASK75).
+'''Procedure:'''
+* Batch for analytical digestion for P92 and P93 with EcoRI-HF and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl
+|Plasmid DNA
+|-
+|1&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF(10&nbsp;U/µl) and PstI-HF (10&nbsp;U/µl) for P92/93, NdeI (10&nbsp;U/µl) for P94
+|-
+|7.5/7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+* 1. band (P92): no mRuby at 700bp visible, only empty vector
+* 2. band (P93): empty vector and EGFR --> perfect
+* 3. band (P94): no signal at all --> repetition of QC-PCR
@@ Line 701: / Line 3,497: @@
 <!--- PLEASE DO NOT TOUCH !!!! -->
 <!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 7 (June 27th - July 3rd)=
+<div class="week" id="Week_7">
+=='''Monday, June 27th'''==
+<div class="receptor">
+=== Sequencing of P67 (EGFR-Signalpeptid) ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+Sequencing batch was prepared after manufacturer's protocol. (15&nbsp;µl of plasmid DNA (100&nbsp;ng) and 2&nbsp;µl sequencing primer (VF2))
+FR11326586
+</div>
+<div class="streptavidin">
+=== Repetition of Quick-Change PCR of P3 (pASK + SAm1) ===
+'''Investigator: Luisa'''
+'''Procedure:'''
+* The QC-PCR was performed according the SOP.
+* Reaction Mix:
+<table cellspacing="0" border="1">
+<tr>
+<td><b>volume</b>
+</td><td><b>reagent</b>
+</td></tr>
+<tr>
+<td>1,25 µl
+</td><td>Primer O21
+</td></tr>
+<tr>
+<td>1,25 µl
+</td><td>Primer O22
+<tr>
+<td>1 µl
+</td><td> dNTP-mix
+</td></tr>
+<tr>
+<td> 5 µl
+</td><td>Pfu-Ultra-II reaction buffer
+<tr>
+<td>1 µl
+</td><td> template DNA (1:10 dilution of p3)
+</td></tr>
+<tr>
+<td> 0,5 µl
+</td><td>Pfu-Ultra-II Polymerase
+<tr>
+<td>40,5 µl
+</td><td> ddH2O
+</td></tr></table>
+* Digestion of PCR-Product with DpnI for 1h at 37°C.
+* Transformation of 10µl into component E.coli XL-1-blue, according to SOP (1h incubation at 37°C necessary despite AmpR).
+</div>
+<div class="receptor">
+=== PCR of Genesynthesis 3 and 4 ===
+'''Investigator: Luisa'''
+'''Aim of Experiment: Amplification of Genesynthesis 3 (contains BAP and IGKappa) and 4 (contains A3C5-tag and BM40)'''
+'''Procedure:'''
+* The PCR was performed according the SOP.
+* Reaction Mix:
+<table cellspacing="0" border="1">
+<tr>
+<td><b>volume</b>
+</td><td><b>reagent</b>
+</td></tr>
+<tr>
+<td> 2,5 µl
+</td><td>Primer VF2
+</td></tr>
+<tr>
+<td> 2,5 µl
+</td><td>Primer VR2
+<tr>
+<td> 1 µl
+</td><td> dNTP-mix
+</td></tr>
+<tr>
+<td> 10 µl
+</td><td> Q5 Polymerase reaction buffer
+<tr>
+<td>1 µl
+</td><td> template DNA (1:10 dilution of p3)
+</td></tr>
+<tr>
+<td> 0,5 µl
+</td><td> Q5-Polymerase
+<tr>
+<td> 18 µl
+</td><td> ddH2O
+</td></tr></table>
+*Setup: iGEM_standard (Promega-cycler)
+<table cellspacing="0" border="1">
+<tr>
+<td><b>temperature</b>
+</td><td><b>time</b>
+</td></tr>
+<tr>
+<td> 98°C
+</td><td> 2min
+</td></tr>
+<tr>
+<td> 98°C
+</td><td> 10sec
+<tr>
+<td> 66°C
+</td><td> 30sec
+</td></tr>
+<tr>
+<td> 72°C
+</td><td> 30sec
+<tr>
+<td> 72°C
+</td><td> 2min
+</td></tr>
+<tr>
+<td> 4°C
+</td><td> hold
+</td></tr></table>
+* the batches were then purified using the Quiagen PCR-Purification Kit.
+</div>
+<div class="receptor">
+=== Analytical digestion and gelelectrophoresis of P88 (pASK75(Steptactin)), P89 (pSB1C3(CMV+CD4) and P90 (pSB1C3(CMV+EGFR-Signal peptide) ===
+'''Investigator: Niklas'''
+'''Aim of experiment: Analytical digestion and gelelectrophoresis of P88 (pASK75 + Streptactin, former F58), P89 (CMV + CD4, former F65) and P90 (CMV + EGFR-signal-peptide, former F66)'''
+'''Procedure:'''
+* Batches for analytical digestions:
+P88: EcoRI
+P89: EcoRI and PstI
+P90: EcoRI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|5,8/2,3/1,8 &nbsp;µl
+|Plasmid DNA (P88/P89/P90)
+|-
+|1&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF(10&nbsp;U/µl)/ PstI
+|-
+|required amount for total volume of 10&nbsp;µl
+|ddH2O
+|}
+[[File:Muc16_P88-90_NA.JPG]]
+</div>
+<div class="receptor">
+===  Ligation of F67 (BirA) and F71 (vector fragment pSB1C3), Transformation of ''E.&nbsp;coli'' XL1 blue afterwards ===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Ligation of F67 (BirA) and F71 (empty pSB1C3), Transformation of ''E.&nbsp;coli'' XL1 blue afterwards.
+'''Procedure:'''
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2,4&nbsp;µl
+|Vektor
+|-
+|7,6&nbsp;µl
+|Insert
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|ddH<sub>2</sub>O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were taken out of stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 750&nbsp;µl LB-medium to each tube.
+* Incubation for 1 hour at 37&nbsp;°C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the cell-culture shaker.
+* next step: analytic digestion of transformation was successful
+</div>
+<div class="receptor">
+=== Digestion of PCR on genesynthesis 3 and 4, and pSB1C3 ===
+'''Investigator: Luisa'''
+'''Aim of experiment: Division of Leptin, IGKappa, A3C5, BM40 and BAP using SapI, HindIII, XbaI, AgeI for both batches.'''
+'''Procedure:'''
+* Batches for analytical digestions:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1 µl each
+|enzyme (SapI, HindIII, XbaI, AgeI)
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|41&nbsp;µl
+|DNA (purified PCR-products of GSY3 and 4)
+|-
+|}
+* Additionally 10µg of the vector P74 was digested with XbaI and AgeI in 100µl batch (2µl of each enzyme, 10µl of Cut-Smart buffer). Digestion was performed over night and purified via gelelectrophoresis and gelextraction according to the manufacturer's protocoll. --> Now labeled F80.
+</div>
+<div class="receptor">
+=== Preparative digestion and gelelectrophoresis of P80 , P78 and P85 ===
+'''Investigator: Julian'''
+'''Aim of experiment: Preparative digestion and gelelectrophoresis of P80 (mRuby3), P78 (NanoLuc) and P85 (Strep-Tag)'''
+'''Procedure:'''
+* Batches for analytical digestions:
+*P80 and P78: EcoRI and AgeI
+*P85: EcoRI and NgoMIV
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10 &nbsp;µl
+|Plasmid DNA
+|-
+|32 &nbsp;µl
+|ddH2O
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1.5&nbsp;µl
+|each enzyme(10&nbsp;U/µl)/ PstI
+|-
+|50&nbsp;µl
+|'''TOTAL'''
+|}
+[[File:Muc16_P78-P80_2806.jpeg]]<br>
+[[File:Muc16_P85_2806.jpeg]]
+</div>
+<div class="receptor">
+===  Ligation of F75 (mRuby) and F76 (NanoLuc) into F74 (pSB1C3 with Strep-Tag) and Transformation into ''E.&nbsp;coli'' XL1 blue ===
+'''Investigator: Luisa'''
+'''Aim of the experiment:''' Ligation of F75 (mRuby) and F76 (NanoLuc) into F74 (pSB1C3+Strep-Tag), Transformation of ''E.&nbsp;coli'' XL1 blue afterwards.
+'''Procedure:'''
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|4,3µl(for F75), 8,2µl (for F76)
+|Vector
+|-
+|12,7µl (F75), 8,8 (F76)
+|Insert
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Ligation was incubated at RT for 1,5h.
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were taken out of stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 15&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* Incubation for 1 hour at 37&nbsp;°C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the incubator.
+</div>
+<div class="general">
+=== Chemical biotinylation of BSA ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* BSA was chemically biotinylated with a 20x and 40x molar excess:
+* 10 ml of 100 mM borate buffer with 50 mM NaCl (pH 8.85)
+* dissolve BSA (10 mg/ml)
+* Add biotin-NHS-ester: 20,5 mg for 40x molar excess
+* reaction over night
+</div>
+=='''Tuesday, June 28th'''==
+<div class="receptor">
+=== Preparative digestion and gelelectrophoresis of P83 (EspP) and P29 (DoubleTerminator) ===
+'''Investigator: Julian'''
+'''Aim of experiment: Preparative digestion and gelelectrophoresis of P83 (EspP) and P29 (DoubleTerminator)'''
+'''Procedure:'''
+* Batches for analytical digestions:
+*P83: EcoRI and SpeI
+*P29: EcoRI and XbaI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6.5/13 &nbsp;µl
+|Plasmid DNA (P83/P29)
+|-
+|35.5/29 &nbsp;µl
+|ddH2O (P83/P29)
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1.5&nbsp;µl
+|each enzyme
+|-
+|50&nbsp;µl
+|'''TOTAL'''
+|}
+*Preparative gelelectrophoresis was performed at 80&nbsp;V for 80&nbsp;min
+[[File:Muc16_P83P29_2806.jpeg]]
+</div>
+<div class="receptor">
+=== Gelelectrophoresis of F73 (pSB1C3 digst. EcoRI, AgeI)  ===
+'''Investigator: Julian'''
+'''Aim of experiment: gelelectrophoresis of P80 (mRuby3), P78 (NanoLuc) and P85 (Strep-Tag)'''
+'''Procedure:'''
+Preparative gelelectrophoresis was performed at 100&nbsp;V for 45&nbsp;min using a pocket spanning over the full width of the 1% agarose gel
+[[File:Muc16_F71_2806.jpeg]]
+</div>
+=='''Wednesday, June 29th'''==
+<div class="receptor">
+=== Transformation of F83 (EspP-Fragment in Double Terminator + pSB1C3), F84 (GSY3 + pSB1C3) F85 (GSY4 + pSB1C3) ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C.
+</div>
+=='''Thursday, June 30th'''==
+<div class="general">
+=== Transformation of new ''E.&nbsp;coli'' XL1-blue (P75), additional plating of untransformated XL1-blue   ===
+'''Aim of experiment: Quality assurance'''
+'''Investigator: Niklas'''
+'''Procedure:'''
+* the new competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 1&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C.
+* additional plating of untransformated XL1-blue on Tet-, Cam-, Amp- and Kan-plates
+'''Result:'''
+* After 12 hous of incubation there were some (~20) colonies on the 50µl-plate transformed with Cam-resistence-plasmids. The transformation has been succesful, though cells grow slow.
+* There were no colonies on the kan-, amp- and cam- plates with the untransformed E.Coli. Hence we can assume that there are no other plasmids with resistences  against kan, amp or cam in our batch of competent cells.
+There are cells on the tet-plate. This was expected.
+</div>
+=='''Friday, June 31th'''==
+<div class="streptavidin">
+=== Transformation of P9 (pASK with Streptavidin WT) and QC-PCR product into new ''E.&nbsp;coli'' XL1-blue   ===
+'''Aim of experiment: Tranforming pASK without NdeI-cutting point into E.coli (two batches from diffrent approches were tested). And Transforming pASK_SA1 into E.coli XL-1-blue.'''
+'''Investigator: Luisa'''
+'''Procedure:'''
+* the new competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 10&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 15&nbsp;min incubation on ice
+* 30&nbsp;sec. heat shock at 42&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube. 1h hour incubation at 37°C.
+* The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30&nbsp;°C.
+</div>
+=Week 8 (July 04&ndash;10)=
+<div class="week" id="Week_8">
+=='''Monday, July 04'''==
+<div class="streptavidin">
+=== Repetition of the Transformation of QC-PCR product into new ''E.&nbsp;coli'' XL1-blue   ===
+'''Aim of experiment: Tranforming pASK without NdeI-cutting point into E.coli (two batches from diffrent approches were tested).'''
+'''Investigator: Luisa'''
+'''Procedure:'''
+* the new competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 10&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 15&nbsp;min incubation on ice
+* 30&nbsp;sec. heat shock at 42&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube. 1h hour incubation at 37°C.
+* The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30&nbsp;°C.
+</div>
+<div class="streptavidin">
+=== Transformation of P9 (Streptavidin in pASK75) into ''E.&nbsp;coli'' BL-21 ===
+'''Aim of experiment: Tranforming pASK with Streptavidin into E.coli BL-21 for Expression.'''
+'''Investigator: Niklas'''
+'''Procedure:'''
+* the new competent ''E.&nbsp;coli'' BL-21 cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 1&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 15&nbsp;min incubation on ice
+* 5&nbspmin. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cells were plated out on Amp-plates (inclusive rescue plate) and incubated over the weekend at 30&nbsp;°C
+</div>
+<div class="receptor">
+=== Transformation of F94 (hGH polyadenylation sequence and Nanoluc with StrepTag) ===
+'''Investigator: Javier'''
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 45&nbsp;sec. heat shock at 42&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium.
+* The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C.
+</div>
+<div class="receptor">
+===Miniprep of E. coli Xl1-Blue transformed with ligation product  P108 and P113 (EspP-Fragment in Double Terminator, F81+F82), P109 and P110 (GSY3+ F73 vector AgeI+XbaI ), P111 and P112 (GSY4+ F73 vector AgeI+XbaI) ===
+'''Investigator: Javier'''
+'''Aim of the experiment:''' Extracting P108 and P113 (EspP-Fragment in Double Terminator, F81+F82), P109 and P110 (GSY3+ F73 vector AgeI+XbaI ), P111 and P112 (GSY4+ F73 vector AgeI+XbaI) from E.coli XL-1-blue
+'''Procedure:'''
+* Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
+* Concentrations:
+<table cellspacing="0" border="1">
+<tr>
+<td><b>Plasmid</b>
+</td><td><b>c [ng/µl]</b>
+</td></tr>
+<tr>
+<td>P108
+</td><td>116,2
+</td></tr>
+<tr>
+<td>P109
+</td><td>86,6
+<tr>
+<td>P110
+</td><td>136,8
+<tr>
+<td>P111
+</td><td>144,8
+<tr>
+<td>P112
+</td><td>163,2
+<tr>
+<td>P113
+</td><td>123,3
+</td></tr></table>
+</div>
+<div class="receptor">
+=== Preparative digestion and gelelectrophoresis of P74 (RFP-Gen.) ===
+'''Investigator: Julian'''
+'''Aim of experiment: Preparative digestion and gelelectrophoresis of P74 (RFP-Gen.) '''
+'''Procedure:'''
+* Batch for analytical digestion:
+*P74: EcoRI and SpeI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2.5&nbsp;µl
+|Plasmid DNA
+|-
+|39.5&nbsp;µl
+|ddH2O
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1.5&nbsp;µl
+|each enzyme
+|-
+|50&nbsp;µl
+|'''TOTAL'''
+|}
+*Preparative gelelectrophoresis was performed at 90&nbsp;V for 45&nbsp;min
+'''Result: '''pSB1C3 (EcoRI und SpeI) F95
+[[File:Muc16_F95_0407.jpeg]]
+</div>
+<div class="receptor">
+=== Cloning of F96 (BirA in pSB1C3) ===
+'''Investigator: Julian'''
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 10&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 5&nbsp;min incubation on ice
+* 30&nbsp;s heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium
+* Incubation at 37 °C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C
+</div>
+=='''Tuesday, July 05th'''==
+<div class="streptavidin">
+=== Preparing of 200 ml TB medium for inoculation of 2 L medium on Thursday   ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* 2.4 g Tryptone 4.8 g yeast extract
+* 800&nbsp;µl Glycerine
+* adjust to 180 ml with ELGA-water
+* seperately: 3.29 g H<sub>2</sub>KPO<sub>4</sub> + 0,46 g K<sub>2</sub>HPO<sub>4</sub> with ELGA water (Volume = 20 ml)
+</div>
+<div class="receptor">
+=== Digestion of F49 (BirA) with EcoRI and SpeI and cloning in F95 (pSB1C3) ===
+'''Investigator: Clemens'''
+'''Procedure:'''
+*Digestion of F49 with EcoRI and SpeI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|20&nbsp;µl
+|Plasmid DNA (F49)
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF(10&nbsp;U/µl)
+|-
+|1 &nbsp;µl
+|SpeI(10&nbsp;U/µl)
+|-
+|23&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+*Digestion was incubated for 1.5&nbsp;h at 37°C
+*Digestion was applied to a 1% agarose-gel
+*Gel ran at 80V for 35&nbsp;min
+[[File:Muc16_digestF49_0507.jpeg]]
+*BirA had a length of 1012&nbsp;bp
+*Upper probe was cut from the gel
+*BirA was purified with gelextraction which was performed by manufacturer's protocol
+*Concentration was measured
+**[F97]= 12.4
+*Ligation of F97 into pSB1C3 (F95)
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.2&nbsp;µl
+|Vector: pSB1C3 (F95)
+|-
+|8.8&nbsp;µl
+|Insert: BirA (F97)
+|-
+|2&nbsp;µl
+|T4 DNA Ligase buffer
+|-
+|fill up to 20&nbsp;µl
+|dd H<sub>2</sub>O
+|-
+|1&nbsp;µl
+|T4 ligase
+|-
+|=21&nbsp;µl
+|'''TOTAL'''
+|}
+*Ligation was incubated at RT for 30&nbsp;min
+*Transformation:
+**Transformation was performed after SOP
+**7&nbsp;µl were used for transformation in E.&nbsp;''coli''&nbsp;XL1blue
+</div>
+<div class="receptor">
+=== Sequencing of P108 - P112 ===
+'''Aim of experiment: Sequencing '''
+'''Investigator: Niklas'''
+'''Procedure:'''
+* sequencing batches after protocol with following barcodes:
+* P108 (EspP-Fragment in Double Terminator (F83)) FR11326572 (VF2)
+* P109 (GSY3+ F73 Leervektor AgeI+XbaI (F84)) FR11326576 (VF2)
+* P110 (GSY3+ F73 Leervektor AgeI+XbaI (F84)) FR11326575 (VF2)
+* P111 (GSY4+ F73 Leervektor AgeI+XbaI (F84)) FR11326574 (VF2)
+* P112 (GSY4+ F73 Leervektor AgeI+XbaI (F84)) FR11326573 (VF2)
+</div>
+<div class="general">
+=== NEB Turbo CaCl<sub>2</sub>-competent cells ===
+'''Investigator: Vivien'''
+'''Procedure:'''
+* Inoculate 50 mL LB with 0.5 mL overnight culture of NEB Turbo cells
+* Incubate at 37 °C for 7 h; final OD<sub>500</sub>: 0.357
+* Very little growth in the course of the last hour; OD<sub>500</sub> 0.45 required
+* Experiment discontinued. Inoculated 3 further colonies in 5 mL LB for o/n growth (37 °C). Repeat experiment on Wed, July 6
+</div>
+<div class="receptor">
+=== Miniprep P114 (NanoLuc + StrepTag + Poly-A in pSB1C3(F94))  ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+*  Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
+</div>
+<div class="receptor">
+=== Analytical digestion and gelelectrophoresis of P114 and P115 ===
+'''Investigator: Niklas'''
+'''Aim of the experiment:'''
+* Analytical digestion and gelelectrophoresis of P114 and P115 (NanoLuc + StrepTag + Poly-A in pSB1C3 K1 and K2)
+'''Procedure:'''
+* Batch for analytical digestion for P114 and P115 with EcoRI+PstI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.75&nbsp;µl
+|Plasmid DNA P114/P115
+|-
+|1&nbsp;µl
+|cut smart (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI
+|-
+|0.5&nbsp;µl
+|PstI
+|-
+|6,25&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Incubation for 45&nbsp;min at 37&nbsp;°C.
+* Analytical gelelectrophoresis was performed at 90&nbsp;V for 60&nbsp;min.
+'''Results:'''
+[[File:Muc16_digestP114_P115_0507.jpeg]]
+{|cellspacing="0" border="1"
+|1&nbsp;kbp ladder DNA ladder
+|'''P114'''
+|'''P115'''
+|-
+|
+|'''X'''
+|'''X'''
+|}
+</div>
+<div class="streptavidin">
+=== Inoculation of Quick change of P88 (pASK75 (Streptactin)) preculture   ===
+'''Investigator: Clemens'''
+'''Procedure:'''
+* four colonies were picked from plate
+* Cells were inoculated in 5&nbsp;mL LB medium (ampicillin 1:1000)
+</div>
+<div class="receptor">
+=== Analytical digestion of P108 and P113 (both EspP + double terminator (F83)) with EoRI and PstI  ===
+'''Investigator: Clemens'''
+'''Procedure:'''
+*Digestion of F49 with EcoRI and SpeI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl
+|Plasmid DNA (P108/P113)
+|-
+|1&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF(10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI(10&nbsp;U/µl)
+|-
+|7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+*Digestion was incubated for 1.5&nbsp;h at 37°C
+*Digestion was applied to a 1% agarose-gel
+*Gel ran at 80V for 35&nbsp;min
+[[File:Muc16_analyt.digest.P108_P113_0507.jpeg]]
+*P108 and P113 showed the right bands
+</div>
+=='''Wednesday, July 06th'''==
+<div class="receptor">
+=== Sequencing of P108 (EspP-Fragment in Double Terminator (F83))   ===
+'''Investigator: >Niklas'''
+'''Procedure:'''
+* sequencing batches after protocol with following barcodes:
+* P108 (EspP-Fragment in Double Terminator (F83)) FR11326572 (VR)
+</div>
+<div class="receptor">
+=== Digestion of P75 (RFP-Generator) with HincII + dephosphorylation  ===
+'''Investigator: Niklas'''
+'''Aim of experiment:''' Blunt-Ligation of BirA into pSB1C3
+'''Procedure:'''
+*Digestion of P75 (RFP-Generator) with HincII + dephosphorylation
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3&nbsp;µl
+|Plasmid DNA (P75)
+|-
+|2&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|HincII
+|-
+|1&nbsp;µl
+|Fast AP (for dephosphorylation)
+|-
+|14.5&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Digestion was incubated for over night at 37°C
+*next steps: PCR of GSY2 with O17 and O18 + phosphorylation, Ligation in digested pSB1C3 afterwards
+</div>
+<div class="receptor">
+=== Cloning of A3C5 Tag into the MiddleLinker-Plasmid  ===
+'''Investigator: Christoph'''
+'''Aim of experiment:''' Cloning of A3C5 Tag into the MiddleLinker-Plasmid
+'''Procedure:'''
+*Digestion of Middle_Linker Plasmid (P69) with AgeI and PstI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|0.3 µl
+|Plasmid DNA (69)
+|-
+|2&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1 µl
+|AgeI
+|-
+|1 µl
+|PstI
+|-
+|1&nbsp;µl
+|Fast AP (for dephosphorylation)
+|-
+|14.5&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|0.3 µl
+|Plasmid DNA (P112)
+|-
+|2&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1 µl
+|NgomIV
+|-
+|1 µl
+|PstI
+|-
+|14.5&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Digestion was incubated for over night at 37°C, heat inactivation at 80°C for 20 min.
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2 µl
+|digested Middle-Linker (F99)
+|-
+|8 µl
+|digested A3C5 (F100)
+|-
+|2 µl
+|10x Ligase Buffer
+|-
+|1 µl
+|Ligase
+|-
+|7 µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Transformation according to SOP in E. coli XL1 blue
+</div>
+<div class="receptor">
+=== Picking of of ''E.&nbsp;coli'' XL1 blue with Streptactin in quickchanged pASK75, F84 (digested GSY3), F85 (digested GSY4) ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* Streptactin in quickchanged pASK75: Colonies were picked from Amp-plates. (10x)
+* F84/F85: Colonies were picked from Cam-plates. (8x each)
+* Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contains 4&nbsp;mL of LB-medium + 4&nbsp;µL of the proper antibiotic.
+* These tubes were transferred in a cell culture shaker at 37&nbsp;°C and were incubated overnight
+</div>
+<div class="receptor">
+=== Quick Change of mRuby Plasmids  ===
+'''Investigator: Christoph'''
+'''Aim of experiment:''' Correction of wrong amino acid within the mRuby sequence
+'''Procedure:'''
+QC according to manufacturers protocol
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10 ng (= 0,3 µl 1:10)
+|Plasmid DNA (80)
+|-
+|5 µl
+|10x Pfu Ultra II Buffer
+|-
+|1.25 µl
+|O23
+|-
+|1.25 µl
+|O24
+|-
+|0.5 µl
+|Pfu Ultra II
+|-
+|1 µl
+|dNTPs
+|-
+|40.7 µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10 ng (= 0,3 µl 1:10)
+|Plasmid DNA (100)
+|-
+|5 µl
+|10x Pfu Ultra II Buffer
+|-
+|1.25 µl
+|O23
+|-
+|1.25 µl
+|O24
+|-
+|0.5 µl
+|Pfu Ultra II
+|-
+|1 µl
+|dNTPs
+|-
+|40.7 µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+*PCR: 2 min. 98°C initial denaturation, 10 sec. 98°C, 30 sec. Annealing st 60 °C, 5 min 68°C, 35 Cycles
+*1 h at 37°C DpnI Digestion
+*Transformation according to SOP in E. coli XL1 blue, QC on mRuby-Strep (F103) was also transformed in E. coli Turbo cells for further investigating the growth rate
+</div>
+<div class="streptavidin">
+=== Miniprep of Quick Change of pASK75-Streptactin + analytical digestion with Nde1  ===
+'''Investigator: Jan'''
+'''Procedure:'''
+*Miniprep using the kit according to the manufacturer's protocol.
+*Although cultures seemed to have grown properly, very low and unreliable DNA concentrations were obtained via Nanodrop measurement and no fragment at all could be detected via analytical agarose gel electrophoresis after 90 minutes digestion with Nde1
+</div>
+<div class="receptor">
+===Creation of competent NEB Turbo cells===
+'''Investigator: Jan'''
+'''Procedure:'''
+* 250 µl of precultures were used to inoculate 50 ml LB-medium
+* After an OD=0.45 was reached, cells were put on ice and made competent according to the manufacturer's protocol
+* 50 µl aliquots of competent cells were frozen in liquid nitrogen and stored at -80°C until further use
+</div>
+<div class="general">
+===Inoculation of a BL21 pBAD-GFP (P60) preculture===
+'''Investigator: Jan'''
+'''Procedure:'''
+* A single clone was picked in order to inoculate 5 ml LB medium (+Cam)
+* Culture was grown overnight at 37°C
+</div>
+<div class="streptavidin">
+===Inoculation of a BL21 preculture for Streptavidin production (P8) ===
+'''Investigator: Jan'''
+'''Procedure:'''
+* A clone was picked for the inoculation of 5 ml LB medium
+* After 6-8 hours of incubation, the 5 ml preculture was used for the inoculation of a 50 ml LB preculture
+</div>
+=='''Thursday, July 07'''==
+<div class="general">
+===PCR Amplification of ''birA'' (GSY 2)===
+'''Investigator: Vivien'''
+'''Aim:''' Amplify ''birA'' gene
+'''Procedure:'''
+* Prepared PCR mix (25&nbsp;&mu;L reaction volume): NEB Q5 High-Fidelity 2&times; Master Mix (12.5&nbsp;&mu;L), ddH<sub>2</sub>O (9.5&nbsp;&mu;L), F29 (1&nbsp;&mu;L), O17 and O18 (1&nbsp;&mu;L each)
+* Cycling protocol: start 1.5&nbsp;min, 98&nbsp;°C; 35 cycles 30&nbsp;s, 98&nbsp;°C &ndash; 45&nbsp;s, 72&nbsp;°C &ndash; 30&nbsp;s, 72&nbsp;°C; final elongation 5&nbsp;min, 72&nbsp;°C; end 4&nbsp;°C
+* Purified ''via'' Quiagen PCR Purification kit following manufacturer's instructions. DNA eluted from column by adding 50&nbsp;&mu;L EB buffer and heating at 37&nbsp;°C for 5&nbsp;min prior to centrifugation.
+'''Results:''' DNA concentration: 82.7&nbsp;ng/&mu;L. Stored as F102 at &ndash;20&nbsp;°C
+</div>
+<div class="streptavidin">
+===Induction of Streptavidin===
+'''Investigator: Vivien'''
+'''Aim:''' Induce streptavidin production
+'''Procedure:'''
+* Inoculated 2&nbsp;L TB medium with 50&nbsp;mL o/n pre-culture and added 2&nbsp;mL ampicillin (10&nbsp;mg/mL in 50% EtOH)
+* Let grow (37&nbsp;°C, 200&nbsp;rpm) until OD<sub>500</sub>=0.622 (''c.'' 2.5&nbsp;h)
+* Induced with anhydrotetracycline (1:10,000 i.e. 200&nbsp;&mu;L of 2&nbsp;mg/mL stock)
+* Let grow (37&nbsp;°C, 200&nbsp;rpm) for 4&nbsp;h
+'''Results:''' Induced culture for harvesting (see below)
+</div>
+<div class="general">
+===Production of eGFP===
+'''Investigator: Clemens, Vivien, Christoph'''
+'''Aim:''' Produce eGFP
+'''Procedure:'''
+* Inoculated 50&nbsp;mL LB+Cam medium with 0.5&nbsp;mL o/n pre-culture
+* Let grow (37&nbsp;°C, 200&nbsp;rpm) until OD<sub>500</sub>=0.58
+* Induced with 0.1&nbsp;mM arabinose (i.e. 100&nbsp;&mu;L of 50&nbsp;mM stock)
+* After 7 h of induction the cells were stored in the fridge overnight for maturation of the GFP-chromophore
+'''Results:'''
+</div>
+<div class="streptavidin">
+===Harvesting of Streptavidin===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Recombinant expression and purification of streptavidin
+'''Procedure:'''
+* After expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
+* The supernatant was discarded, and the pellet was transferred into a Falcon and frozen
+* next steps: resuspending and homogenizing in the PANDA
+</div>
+=='''Friday, July 08'''==
+<div class="general">
+=== Analytical Digest of mRuby3 Constructs   ===
+'''Aim of experiment: Verify integration of mRuby3 constructs in F103 and F104'''
+'''Investigator: Vivien'''
+'''Procedure:'''
+* Mixed 16&nbsp;&mu;L F103 (or 8&nbsp;&mu;L F104 plus 8&nbsp;&mu;L ddH<sub>2</sub>O) with 2&nbsp;&mu;L 10&times; CutSmart buffer and 1&nbsp;&mu;L each of EcoRI-HF and PstI-HF (20&nbsp;&mu;L total volume)
+* Incubated for 45&nbsp;min at 37&nbsp;°C
+* Subjected to gel electrophoresis (1% agarose, 80&nbsp;V, 120&nbsp;min)
+'''Results:''' No band around 700&nbsp;bp as expected for mRuby3 constructs
+</div>
+<div class="receptor">
+=== Picking clones and inoculating cultures for F101 and F103 ===
+'''Investigator: Jan'''
+'''Procedure:'''
+* All clones available (only two for F101, one for F103) were picked and used to inoculate 5 ml of LB medium containing the appropriate antibiotic
+* Cultures were incubated at 37°C overnight
+</div>
+<div class="streptavidin">
+=== Solubilization, lysis and unfolding of streptavidin ===
+'''Investigator: Jan'''
+'''Procedure:'''
+* According to protocol -> lysis of pellet (19.2 g) in 58 ml lysis buffer (50 mM Tris/HCl pH 8, 1 mM EDTA)
+* As only two liters of medium were used, the Panda couldn't be utilized for cell lysis -> French Press was used
+* Cells were additionally submitted to ultrasonic treatment
+* Centrifugation of cells, casting away the supernatant and resolubilizing the pellet in 5 ml GdmCl (6M, pH 1.5)
+</div>
+<div class="streptavidin">
+=== Sequencing of P88 ===
+'''Aim of experiment: Verification of QC  '''
+'''Investigator: Julian'''
+'''Procedure:'''
+Sequencing batch was prepared after manufacturer's protocol. (15&nbsp;µl of plasmid DNA (100&nbsp;ng) and 2&nbsp;µl sequencing primer (PR1))
+FR11326565
+</div>
+<div class="receptor">
+=== Transformation of P75 (RFP-Generator), F101 (middle linker+ A3C5), P125 (dig. GSY4) into ''E.&nbsp;coli'' XL1-blue and P75 in NEB Turbo ''E.&nbsp;coli'' ===
+'''Investigator: Niklas, Vivien'''
+'''Procedure:'''
+* the competent ''E.&nbsp;coli'' cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 1&nbsp;µl of DNA (6&nbsp;µl for Ligation F101) was added to 50&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbspmin. heat shock at 37&nbsp;°C
+* 30&nbsp;min incubation on ice
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cells were plated out on Cam-plates/Amp-plate for F101 (inclusive rescue plate) and incubated over the weekend at 30&nbsp;°C
+</div>
+<div class="receptor">
+=== QuickChange-PCR of P80 (O23 and O24) and P100 (O19 and O20) ===
+'''Investigators: Niklas'''
+'''Aim of the experiment:''' Changing of amino acid
+'''Procedure:'''
+* the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1&nbsp;µl Polymerase is added)
+* Annealing at 55°C
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.25µl
+|O23/O24 and O19/O20
+|-
+|0,5&nbsp;µl
+|dNTP-mix
+|-
+|1&nbsp;µl
+|1:100 P80 / P100
+|-
+|2.5&nbsp;µl
+|Pfu Ultra II-buffer
+|-
+|0.5&nbsp;µl
+|Pfu Ultra II Polymerase
+|-
+|19.25&nbsp;µl
+|dd H<sub>2</sub>O
+|-
+|4 x 25&nbsp;µl
+|'''TOTAL'''
+|}
+</div>
+<div class="receptor">
+=== Preperative gelelektrophoresis of F102 (PCR of BirA) + phosphorylation and ligation into pSB1C3 ===
+'''Investigator: Luisa'''
+'''Aim of experiment:''' Blunt-Ligation of BirA into pSB1C3
+'''Procedure:'''
+*The whole PCR-product was applied to a 1% agorose gel. After runnig the gel two lines where visible: one at 1000Bp and one at ~500Bp.
+*The 1000 Bp band was cut out and purified with the Gelextraction kit according to manufacturer's protocoll. Concentration: 41,5ng/µl.
+*The DNA was phosphorylated as follows:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|DNA (~1pmol)
+|-
+|2&nbsp;µl
+|Ligase buffer (10x)
+|-
+|1&nbsp;µl
+|T4 Polynukleotide-Kinase (for phosphorylation)
+|-
+|2&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*The batch was incubated for 20 min at 37°C and then the enzyme was inactivated for 10 min at 75°C.
+*The phosphorylated DNA was then ligated into prepared (HincII-digested) pSB1C3 as follows:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2,3&nbsp;µl
+|Vector
+|-
+|7,7&nbsp;µl
+|Insert (BirA)
+|-
+|2&nbsp;µl
+|Ligase Buffer (10x)
+|-
+|1&nbsp;µl
+|T4 Ligase
+|-
+|7&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*next steps: Transformation into E.coli Xl-1-blue.
+</div>
+<div class="receptor">
+=== Digestion of P78, P123 (for BAP-Nanoluc-construct),P122 (IgKappa for CMV-IgKappa-construct), P89, P114 (for CMV-EGFR-Nanoluc-StrepTag-PolyA-construct) ===
+'''Investigator: Luisa'''
+'''Aim of experiment:''' Getting of BAP-Nanoluc-construct, CMV-IgKappa-construct and CMV-EGFR-Nanoluc-StrepTag-PolyA-construct.
+'''Procedure:'''
+* DNA was digested according to the following table:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3&nbsp;µg (for P78, P123 and P122) and 1,5&nbsp;µg (for P89, P114)
+|DNA
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1,5&nbsp;µl of NgoMIV and PstI
+|for P78
+|-
+|1,5&nbsp;µl of AgeI and PstI
+|for P123
+|-
+|1,5&nbsp;µl of XbaI and PstI
+|for P122
+|-
+|1,5&nbsp;µl of AgeI and PstI
+|for P189
+|-
+|1,5&nbsp;µl of NgoMIV and PstI
+|for P123
+|-
+|up to 50µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:''' Concentrations: P78 now F106: 2,7 ng/µl, P89 now F107: 14,4 ng/µl. Gelextractions of P114, P122 and P123 didn't contain DNA. (To few DNA available)
+*next steps: Retransformation of verified clones (P114, P89) into Xl-1-blue for amplification of plasmid.
+Repetition of digestion of P122 and P123 with more DNA (10µg!), then Gel with 100Bp ladder!
+</div>
+<div class="receptor">
+=== Repetition of digestion of  P123 (BAP for BAP-Nanoluc-construct) and P122 (IgKappa for CMV-IgKappa-construct) ===
+'''Investigator: Luisa'''
+'''Aim of experiment:''' Getting of BAP-Nanoluc-construct, CMV-IgKappa-construct
+'''Procedure:'''
+* DNA was digested according to the following table:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µg &rarr; 20µl
+|DNA
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1,5&nbsp;µl of AgeI and PstI
+|for P123
+|-
+|1,5&nbsp;µl of XbaI and PstI
+|for P122
+|-
+|up to 50µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+*Incubation at 37°C over night.
+*next steps: Gel with 100Bp ladder and Gelex. Then Ligation with prepared vectors from former digestion (F106 an F63)
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 9, July 11&ndash;17=
+<div class="week" id="Week_9">
+=='''Monday, July 11'''==
+<div class="general">
+=== MiniPreps of pSb1C3-Middle Linker+A3C5, -BM40, -CMV-EGFR Retrafo, Streptactin in QC pASK75  ===
+'''Investigator: Christoph'''
+'''Aim of the experiment:''' Plasmid preparation, analytic digestion, sequencing
+'''Procedure:'''
+* MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Analytic digestion with 0.25 ''µ''L EcoRI, 0.25 ''µ''L PstI (HF) for pSB1C3 plasmids and 0.5 µl NdeI for pASK75-Streptactin, 1 ''µ''L SmartCut Buffer, 3 ''µ''L plasmid DNA, 5.5 ''µ''L H<sub>2</sub>O
+* 5 ''µ''L on 1% agarose gel electrophoresis
+* plasmid assignment was tricky because of confusion during the weekend Minipreps
+'''Results:'''
+*  pASK75-Streptactin clone 1 and 2 were not visible
+*  verified Plasmid names are available after sequencing
+* Lane 1: 5 µl 1 kb Ladder
+* Lane 2: 5 ''µ''L Plasmid F101 K1 (seems to be pSB1C3-RFP-Generator)
+* Lane 3: 5 ''µ''L Plasmid F101 K2 (seems not to be pSB1C3-RFP-Generator)
+* Lane 4: 5 µl 100 bp Ladder
+* Lane 5: 5 ''µ''L P125 K1 (seems not to be pSB1C3-RFP-Generator)
+* Lane 6: 5 ''µ''L P125 K2 (seems to be pSB1C3-RFP-Generator)
+[[File:Muc16_160711_analytic_digestion_cg.jpeg|500px]]
+</div>
+<div class="receptor">
+=== Preperative digestion of NanoLuc + StrepTag + Poly-A (F112) and cloning behind CMV-EGFR (F107)  ===
+'''Investigator: Christoph, Niklas'''
+'''Aim of the experiment:''' preperative digestion for cloning of the construct behind of CMV-EGFR
+'''Procedure:'''
+* 15 µl P115 (NanoLuc + StrepTag + Poly-A), 1 µl NgoMiV, 1 µl PstI, 3 µl CutSmart buffer, 10 µl H2O
+* Incubation for 2 h at 37°C
+* 1% gel electrophoresis
+Photo
+* gel extraction according to SOP
+* Ligation of 2 µl F107 (AgeI, PstI) + 8 µl F112 (NgomIV, PstI) with 2 µl  Ligase buffer, 7 µl ddH<sub>2</sub>O, 1 µl T4-Ligase for 40 minutes
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).
+</div>
+<div class="receptor">
+=== Cloning of Nanoluc behind BAP  ===
+'''Investigator: Christoph, Niklas'''
+'''Aim of the experiment:''' Cloning of Nanoluc behind BAP based (testing fast cloning strategy)
+'''Procedure:'''
+* 5 µl P78 (Nanoluc), 0.5 µl NgoMiV, 0.5 µl PstI, 1 µl CutSmart buffer, 2.5 µl H2O, 0.5 SacI = F108
+* 4 µl P123 (pSB1C3-BAP), 0.5 µl AgeI, 0.5 µl PstI, 1 µl CutSmart buffer, 3 µl H2O,  1 µl FastAP = F109
+* Incubation for 2 h at 37°C, 15 min heat inactivation
+* Ligation: 2 µl F108 (Nanoluc) + 8 µl F109 (BAP), 2 µl buffer, 1 µl Ligase, 7 µl H2O
+*Transformation:
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).
+</div>
+<div class="receptor">
+=== Gel extraction of IgKappa (F111) and cloning behind CMV in pSB1C3 (F63)  ===
+'''Investigator: Christoph, Niklas'''
+'''Aim of the experiment:''' gel extraction after digestion for cloning of the construct behind of CMV
+'''Procedure:'''
+* 1% gel electrophoresis
+Photo
+* gel extraction according to SOP
+* Ligation of 6.1 µl F111 ( XbaI, PstI) + 3.9 µl F63 (SpeI, PstI) with 2 µl  Ligase buffer, 7 µl ddH<sub>2</sub>O, 1 µl T4-Ligase for 40 minutes
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).
+</div>
+<div class="receptor">
+=== Retrafo of P123 (digest. GSY3-BAP)  ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 1&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).
+</div>
+<div class="receptor">
+=== Digestion of quickchanged mRuby (without StrepTag) and transformation of ''E.&nbsp;coli'' XL1-Blue afterwards  ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* the PCR-product is digested by 1 µl DpnI (cuts methylated DNA)
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a new chlorampenicol plate (=rescue plate).
+* next steps: 4 Minipreps, test digestion, Sequencing
+</div>
+<div class="receptor">
+=== QuickChange-PCR of P100 (O23 and O23) ===
+'''Investigators: Julian, Niklas'''
+'''Aim of the experiment:''' Changing of amino acid in mRuby3
+'''Procedure:'''
+* the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1&nbsp;µl Polymerase is added)
+* Annealing at 55°C
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.25µl
+|O23/O24
+|-
+|0,5&nbsp;µl
+|dNTP-mix
+|-
+|1&nbsp;µl
+|1:100 P100
+|-
+|2.5&nbsp;µl
+|Pfu Ultra II-buffer
+|-
+|0.5&nbsp;µl
+|Pfu Ultra II Polymerase
+|-
+|19.25&nbsp;µl
+|dd H<sub>2</sub>O
+|-
+|4 x 25&nbsp;µl
+|'''TOTAL'''
+|}
+</div>
+<div class="receptor">
+=== Repeated digestion of P75 (RFP-Generator) with HincII + dephosphorylation  ===
+'''Investigator: Julian'''
+'''Aim of experiment:''' Blunt-Ligation of BirA into pSB1C3
+'''Procedure:'''
+*Digestion of P75 (RFP-Generator) with HincII + dephosphorylation
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA (P75)
+|-
+|2&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1&nbsp;µl
+|HincII
+|-
+|1&nbsp;µl
+|Fast AP (for dephosphorylation)
+|-
+|11&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Digestion was incubated for 2 hours at 37°C
+</div>
+<div class="receptor">
+=== Ligation of phosphorylated F102 (PCR of BirA) into F113 (RFP-Generator P75 digest. HincII) ===
+'''Investigator: Julian'''
+'''Aim of experiment:''' Blunt-Ligation of BirA into pSB1C3
+'''Procedure:'''
+*The phosphorylated DNA (prepared on July 8th) was ligated into F113 (HincII-digested RFP-Generator) as follows:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|4,5&nbsp;µl
+|Vector F113
+|-
+|5,7&nbsp;µl
+|Insert (BirA)
+|-
+|2&nbsp;µl
+|Ligase Buffer (10x)
+|-
+|1&nbsp;µl
+|T4 Ligase
+|-
+|7&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*next steps: Transformation into E.coli NEB Turbo.
+</div>
+==Tuesday, July 12==
+<div class="receptor">
+===Transformation of BirA&ndash;RFP generator ligation (F114) and Re-Transformation of P114===
+'''Investigator: Vivien'''
+'''Aim:''' Transform NEB Turbo cells
+'''Procedure:'''
+* Followed standard transformation protocol (SOP) using 1&nbsp;&mu;L and 10&nbsp;&mu;L of P114 and F114, respectively
+* Incubated at 37&nbsp;°C for 1:10&nbsp;h
+* Plated on LB Cam (50&nbsp;&mu;L + rescue)
+* Incubated at 37&nbsp;°C (start 12:30)
+</div>
+<div class="general">
+===Arabinose Induction Experiment: pBAD&ndash;GFP===
+'''Investigator: Vivien'''
+'''Aim:''' Test different induction concentrations of arabinose
+'''Procedure:'''
+* Of 30&nbsp;°C o/n culture, filled 5&nbsp;mL each into four 10&nbsp;mL culture tubes
+* Induced with 0, 0.1, 1, and 10&nbsp;mM final conc. of arabinose
+* Took 0.5&nbsp;mL sample each and stored at 4&nbsp;°C
+* Incubated 5&nbsp;mL cultures at 30&nbsp;°C for 4&nbsp;h
+* Took another 0.5&nbsp;mL sample each and stored at 4&nbsp;°C
+</div>
+<div class="receptor">
+===Picking Colonies of F101 (P69 Middle Linker &ndash; P112 A3C5)===
+'''Investigator: Vivien'''
+'''Aim:''' Pick transformed colonies
+'''Procedure:'''
+* Picked 3 colonies off plate with transformed cells
+* Let grow at 37&nbsp;°C in LB Amp (start 11:50&nbsp;am)
+</div>
+<div class="receptor">
+===Picking Colonies of F123 (BAP)===
+'''Investigator: Vivien'''
+'''Aim:''' Pick transformed colonies
+'''Procedure:'''
+* Picked 2 colonies off plate with transformed cells
+* Let grow at 37&nbsp;°C in LB Cam (start 17:00)
+</div>
+<div class="streptavidin">
+===Verification of succesful Quickchange of P141 (pASK75 with Streptactin)===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* the Plasmid (5 µl) is digested by 0.5 µl NdeI (Addiition of 1 µl cut smart and 3.5 µl ddH2O)
+* since the quickchange should eliminate the second Nde-restriction site, there should be one band on the gel
+'''result:'''
+* there is no band on the gel (the experiment was repeated multiple times showing the same results)
+* '''therefore new primers are designed and ordered'''
+</div>
+<div class="streptavidin">
+===Refolding of Streptavidin===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* the sample (pelett dissolved in 6M GdmCl)was spun down (4°C, 20 mins, 18,000 rpm)
+* the supernatant was transferred carefully into a falcon tube and the pellet was cast away
+* the supernatant was added dropwise to 1 X PBS (500 ml) and stirred over night
+</div>
+<div class="receptor">
+===Colony PCR of F110 (BAP+Nanoluc)===
+'''Investigator: Vivien, Niklas'''
+'''Aim:''' Amplification
+'''Procedure:'''
+* samples were prepared with 5 µL Q5-Mastermix, 1 µl VF2-, 1 µL VR-Primer, 2 µL ddH20
+* four clones were picked and added to the samples respectively
+* PCR- cycles according to SOP
+* Lane 1: 1 kb Ladder, Lane 2-5: clones 1-4, 10 µl each
+[[File:Muc16_ColonyPCR_F110_1307.jpeg|500px]]
+</div>
+<div class="receptor">
+=== Preparative digestion and gelelectrophoresis of P37 and P26 ===
+'''Investigator: Julian'''
+'''Aim of experiment: Preparative digestion and gelelectrophoresis of P137 (BM40)and P26 (CMV)'''
+'''Procedure:'''
+* Batches for analytical digestions:
+*P137: EcoRI and XbaI
+*P26: EcoRI and SpeI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|23/7 &nbsp;µl
+|Plasmid DNA P137/P26
+|-
+|19/35 &nbsp;µl
+|ddH2O P137/P26
+|-
+|5&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1.5&nbsp;µl
+|each enzyme(10&nbsp;U/µl)
+|-
+|50&nbsp;µl
+|'''TOTAL'''
+|}
+*Preparative gelelectrophoresis was performed at 90&nbsp;V for 60&nbsp;min
+*The whole PCR-product was applied to a 1% agorose gel. After runnig the gel two lines where visible: one at 1000Bp and one at ~500Bp.
+*The 600/2100 bp band (P26/P137) was cut out and purified with the Gelextraction kit according to manufacturer's protocoll. Concentration: 20.4/33.1&nbsp;ng/µl. (F115/F116)
+[[File:Muc16_P137-P26_1207.jpeg]]
+</div>
+<div class="receptor">
+=== Ligation of F115 into F116 ===
+'''Investigator: Julian'''
+'''Aim of experiment:''' Ligation of F115 (CMV) into F116 (BM40 in pSB1C3)
+'''Procedure:'''
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|4,3 &nbsp;µl
+|Vector F116 (BM40 in pSB1C3)
+|-
+|5,7&nbsp;µl
+|Insert F115(CMV)
+|-
+|2&nbsp;µl
+|Ligase Buffer (10x)
+|-
+|1&nbsp;µl
+|T4 Ligase
+|-
+|7&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*next steps: Transformation into E.coli NEB Turbo.
+</div>
+<div class="receptor">
+=== Transformation of F117 (CMV in pSB1C3 with BM40), F118 (QC P100), F119 (QC P80) and P26 (CMV; Retrafo) ===
+'''Investigator: Julian'''
+'''Aim of the experiment:''' Transformation of CMV in pSB1C3 with BM40 (F117), QC P100 (F118), QC P80 (F119) and P26 in NEB Turbos(F117)/XL1 blue
+'''Procedure:'''
+transformation in competent E. coli NEB Turbo (F117)/XL1 blue (rest) according to protocol + rescue
+'''Result:'''
+plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+==Wednesday, July 13==
+<div class="receptor">
+=== QuickChange-PCR of P80 (O23 and O24) ===
+'''Investigators: Christoph'''
+'''Aim of the experiment:''' Changing of amino acid in mRuby3
+'''Procedure:'''
+* the batches were split, each batch contained only one primer, the batches were pooled after 15 cycles (1&nbsp;µl Polymerase is added)
+* Annealing at 55°C
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.25µl
+|O23/O24
+|-
+|0,5&nbsp;µl
+|dNTP-mix
+|-
+|1&nbsp;µl
+|1:100 P80
+|-
+|2.5&nbsp;µl
+|Pfu Ultra II-buffer
+|-
+|0.5&nbsp;µl
+|Pfu Ultra II Polymerase
+|-
+|19.25&nbsp;µl
+|dd H<sub>2</sub>O
+|-
+|4 x 25&nbsp;µl
+|'''TOTAL'''
+|}
+Cycling was performed according to SOP.
+</div>
+<div class="general">
+=== MiniPrep of Middle Linker-A3C5 construct  ===
+'''Investigator: Christoph '''
+'''Aim of the experiment:''' MiniPrep two colonies of Middle Linker-A3C5 construct
+'''Procedure:'''
+* MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Both plasmids were sent to sequencing without analytical digestion because of the short lenght
+</div>
+<!--- this closes the week -->
+</div>
+<div class="general">
+=== Cloning of F120 (CMV-IgKappa) and F121 (CMV+EGFR / Nanoluc+StrepTag+PolyA) ===
+'''Investigator: Christoph'''
+'''Aim of the experiment:''' Ligations of F120 (CMV-IgKappa) and F121 (CMV+EGFR / Nanoluc+StrepTag+PolyA) and transformation
+'''Procedure:'''
+* Ligation mixtures were prepared as following:
+* F120: 	5 μL F63, 5 µL F111, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* F121: 	3 μL F107, 7 μL F112, 2 μL Ligase buffer, 7 μL ddH2O, 1 μL Ligase
+* Ligation was incubated for 30 min. at room temperature
+* transformation was performed according to SOP (with 100 µl cells and 20 µl ligation mix) and plating in LB+Cam agar
+</div>
+==Thursday, July 14==
+<div class="receptor">
+===MiniPreps of Overnight Cultures===
+'''Investigator: Vivien'''
+'''Aim:''' Prep plasmid DNA of P26, F110, F117, F114, P114, and P118
+'''Procedure:'''
+* MiniPrep performed according to manufacturer's instructions with Qiagen kit
+* Prior to eluting, 50&nbsp;&mu;L EB buffer was applied to the membrane, and the columns were heated at 37&nbsp;°C for 7&nbsp;min
+'''Results:''' Plasmid DNA solutions of the following concentrations: P26 (a: 55.1&nbsp;ng/&mu;L; b: 48.1&nbsp;ng/&mu;L); F110 (K2: 150.1&nbsp;ng/&mu;L; K3: 173.0&nbsp;ng/&mu;L); F117 (a: 257.7&nbsp;ng/&mu;L; b: 159.0&nbsp;ng/&mu;L; CMV/BM40: 133.2&nbsp;ng/&mu;L); F114 (83.1&nbsp;ng/&mu;L); P114 (a: 26.1&nbsp;ng/&mu;L; 170.7&nbsp;ng/&mu;L); P118 ('''F118?''') (a: 248.0&nbsp;ng/&mu;L; 53.2&nbsp;ng/&mu;L; 241.3&nbsp;ng/&mu;L). F110 (K2: FR12904474; K3: FR12904473) and F117 (a: FR12904477; b: FR12904476; CMV/BM40: FR12904475) were sent for sequencing with VF2.
+</div>
+<div class="receptor">
+=== DpnI Digest of mRuby3 QC and Transformation===
+'''Investigator: Vivien'''
+'''Aim:''' Digest original-sequence plasmid and transform obtained pure quick-changed plasmid
+'''Procedure:'''
+* QC was digested with DpnI (40&nbsp;&mu;L QC, 5&nbsp;&mu;L 10&times; CutSmart buffer, 3.5&nbsp;&mu;L ddH<sub>2</sub>O, 1.5&nbsp;&mu;L DpnI = 50&nbsp;&mu;L) at 37&nbsp;°C for 2&nbsp;h
+* Digest (10&nbsp;&mu;L) was directly transformed into Turbo cells following SOP (including 1&nbsp;h incubation time prior to plating due to chloramphenicol resistance)
+* Plated 50&nbsp;&mu;L on LB Cam + rescue plate
+* Incubated at 37&nbsp;°C
+'''Result:''' two plates; remaining digest stored at 4&nbsp;°C in styrofoam tube rack
+</div>
+=='''Friday, July 15'''==
+<div class="general">
+=== Inoculation of mRuby Quick change, F120 (CMV+IgKappa) and F121 (CMV+EGFR/Nanoluc+StrepTag+PolyA) preculture and miniprep   ===
+'''Investigator: Niklas, Clemens'''
+'''Procedure:'''
+* 6 colonies were picked from plate
+* Cells were inoculated in 5&nbsp;mL LB medium (Cam 1:1000)
+* Fragments were minipreped following manufacturer's protocol (QiaPrep, Qiagen)
+* Fragments were renamed receiving a P number
+</div>
+<div class="streptavidin">
+=== Quickchange of P88 (pASK75(Streptactin)) with O-029 and O-030===
+'''Investigator: Clemens'''
+'''Aim:''' Quickchange pASK75(Streptactin) to erase one NdeI restriction site
+'''Procedure:'''
+* For quickchange two seperate batches were prepared:
+* 1. batch: 0.7&nbsp;µL O-029, 0.5&nbsp;µL dNTP mix, 2.5&nbsp;µL buffer, 0.5&nbsp;µL Pfu ultra polymerase, 1.5&nbsp;µL P88
+* 2. batch: 0.7&nbsp;µL O-030, 0.5&nbsp;µL dNTP mix, 2.5&nbsp;µL buffer, 0.5&nbsp;µL Pfu ultra polymerase, 1.5&nbsp;µL P88
+* first stage of quickchange PCR was performed as following:
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial Denaturation||98||30
+|-
+|rowspan = "3"|15 cycles||98||10
+|-
+|55||30
+|-
+|68||5
+|-
+|final Extension||68||5
+|-
+|Hold||4||ꝏ
+|}
+* PCR batches were mixed and 0.5&nbsp;µL pfu ultra polymerase was added
+* Second stage of quickchange PCR was performed as in the following:
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial Denaturation||98||30
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|55||30
+|-
+|68||5
+|-
+|final Extension||68||5
+|-
+|Hold||4||ꝏ
+|}
+</div>
+<div class="receptor">
+=== Cloning of P79 (Nanoluc) into P147 (pSB1C3(BAP))===
+'''Investigator: Clemens'''
+'''Aim:'''
+'''Procedure:'''
+* 7&nbsp;µL P79 were digested with NgOMIV and PstI
+* 10&nbsp;µL P147 were digested with AgeI and PstI
+* Digestion products were run on a 1% agarose gel
+* Both fragments could be cut from the gel
+* Fragments were purified by gelectraction following manufacturer's protocol (Qiagen)
+*Fragments were renamed:
+** digest P78= F123
+** digest P147= F124
+* 9,5&nbsp;µL F124 and 0.5&nbsp;µL F123 were ligated following manufacturers protocol (T4 DNA ligase, Thermo scientific)
+* NEB Turbo were transformed with 7&nbsp;µL of F125 (ligation F123+F124) following SOP
+* Cells were plated on CAM LB medium and placed in the incubator at 37°C
+</div>
+<div class="receptor">
+=== Cloning of P145 (Middle Linker +A3C5) and P146 (Middle Linker +A3C5) into F70 (Vector fragment pSB1C3)===
+'''Investigator: Niklas, Clemens'''
+'''Procedure:'''
+*Ligation:
+** 2,5&nbsp;µL P145 and 1&nbsp;µL P146 were pooled and digested with NgOMIV and SpeI for 1h at 37°C.
+** Full digestion was ligated into 1&nbsp;µL F70
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' XL1-Blue cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Add 1&nbsp;ml LB medium to each tube
+* Incubation for 55&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 60&nbsp;µl of the cell suspension was plated on one chloramphenicol plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 60&nbsp;µl of LB-medium and this concentrated cell suspension was plated again on a chlorampenicol plate (=rescue plate).
+</div>
+<div class="receptor">
+=== Test digestion of P164 (BirA blunt end ligation) (after miniprep) and P161, P162, and P163 (all QC mRuby)===
+'''Investigator: Niklas, Clemens'''
+'''Aim:''' Test digestion to see which plasmids contain the right insert
+'''Procedure:'''
+* 150&nbsp;ng of plasmid DNA were digested with EcoRI and PstI following SOP
+* The whole batch was applied to a 1% gel to check for cut inserts.
+'''Results:'''
+FOTO
+* Blunt end ligation seems to not have worked (P164)
+* P161, P162 and P163 all still carry the insert
+Sequenced: P161= FR12904472 (NA)
+</div>
+<div class="streptavidin">
+===Harvesting of Streptavidin===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Recombinant expression and purification of streptavidin
+'''Procedure:'''
+* After precipitation in 70 % ammonium sulfate the soluton was spun down in the centrifuge (4°C, 11000 rpm, 40 mins)
+* The supernatant was discarded, and the pellet was dissolved in 2.2 M ammonium sulfate (18 mL)
+* the sample was spun down in the centrifuge (4°C, 15000 rpm, 30 mins)
+* the pellet was dissolved in 1X PBS(16 mL)
+* next steps: last centrifugation and dialysis against Tris/Hcl (see plan on board)
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 10, July 18&ndash;24=
+<div class="week" id="Week_10">
+=='''Monday, July 18'''==
+<div class="receptor">
+=== Inoculation of precultures for miniprep of F125 (pSB1C3(BAP-NanoLuc)) and F122 (pSB1C3(Middlelinker-A3C5))===
+'''Investigator: Clemens'''
+'''Aim of the experiment: '''
+* Miniprep, analytical digestion, analytical gel, sequencing
+'''Procedure:'''
+* Three colonies were picked from each plate (F125, F122)
+* Inoculation was performed according to SOP
+* Cells grew for 5h
+** Cells onlygrew in cultures with F125 (In cultures with F122 there was no pelet)
+* Miniprep was performed according to manufactrer's protocol
+* Samples were renamed:
+** F125 K1: P168
+** F125 K2: P169
+** F125 K3: P170
+* Analytical digestion:
+** Each plasmid was digested with EcoRI and PstI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P168/P169/P170
+|-
+|1&nbsp;µl
+|Cutsmart (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI(10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI (20&nbsp;U/µl)
+|-
+|1&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+Foto:
+*Lane 1: 1kb ladder
+*Lane 2: P168
+*Lane 3: P169
+*Lane 4: P170 --> right signals (2000 bp, ~600 bp(BAP-NanoLuc)
+*Send for sequencing:
+**P170: FR12904468 (VF2)
+</div>
+<div class="receptor">
+=== Analytical digestion of P149 , P150 (both pSB1C3(CMV-IgKappa)), P151, P152 (both pSB1C3(CMV-EGFR-NanoLuc-StrepTag-polyA)), P153, P154 (both QC pSB1C3(mRuby3))===
+'''Investigator: Clemens'''
+'''Aim of the experiment: '''
+Analytical digeston to find out if the cloning was successful
+'''Procedure:'''
+* measure concentrations of Plasmids (see inventary list)
+* Analytical digestion:
+** Each plasmid was digested with EcoRI and PstI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3&nbsp;µl
+|Plasmid DNA P149/ P150/ P151/ P152/ P153/ P154
+|-
+|1&nbsp;µl
+|Cutsmart (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI(10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI (20&nbsp;U/µl)
+|-
+|5&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+Foto:
+*Lane 1: 1kb ladder
+*Lane 2: P149 --> right signals (2000bp; 730bp)
+*Lane 3: P150 --> right signals (2000bp; 730bp)
+*Lane 4: P151
+*Lane 5: P152 --> right signals (2000bp; 1626bp)
+*Lane 6: P153 --> very weak signal
+*Lane 7: P154 --> right signals (2000bp; 700bp)
+*Send for sequencing:
+** P150: FR12904471 (VF2)
+** P152: FR12904470 (VF2)
+**P154: FR12904469 (VF2)
+</div>
+<div class="streptavidin">
+=== Transformation of QC of P88 (pASK75(Streptactin)) ===
+'''Investigator: Clemens'''
+'''Aim of the experiment: '''
+* See if quickchange has worked
+'''Procedure:'''
+* NEB Turbo cells were transformed with 10&nbsp;µl of QC P88 according to SOP
+* Cells were plated on LB medium (Amp) and incubated at 37°C
+</div>
+<div class="receptor">
+=== Digestion of P165 (pSB1C3(CMV-BM40) and cloning of F112 (Nanoluc-StrepTag-polyA) into P165 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment: '''
+* Create biobrick: CMV-BM40-Nanoluc-StrepTag-polyA
+'''Procedure:'''
+* Preparative digestion batch was prepared as in the following:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA P156
+|-
+|3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl
+|AgeI(10&nbsp;U/µl)
+|-
+|1&nbsp;µl
+|PstI(20&nbsp;U/µl)
+|-
+|10&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestion was seperated by gelelectrophoresis
+'''Results:'''
+Foto:
+* Lane 1: 1kb ladder
+* Lane 2: F126 (digest P165) --> right length
+'''Procedure:'''
+* Fragment was cut from the gel and purified by gelextraction which was performed by manufacturer's protocol (Qiagen)
+* F126 was ligated with F112
+Ligation batch:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2&nbsp;µl
+|Vector DNA F126
+|-
+|18&nbsp;µl
+|Insert DNA F112
+|-
+|3&nbsp;µl
+|T4 ligation buffer (10x)
+|-
+|6&nbsp;µl
+|T4 ligase
+|-
+|&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Ligation was incubated at 37°C for 30 min
+* NEB Tubros were transformed with F127 (lig. F112+F126)
+* Cells were plated on LB medium (Cam)
+</div>
+=='''Tuesday, July 19'''==
+<div class="receptor">
+===Inoculation of Precultures of F127 (pSB1C3(CMV-BM40-Nanoluc-StrepTag-polyA))===
+'''Investigator: Clemens'''
+'''Aim:''' Prepare cells for miniprep of plasmids
+'''Procedure:'''
+* six colonies were picked and inoculated in LB medium (CAM)
+* Plates were incubated on a shaker at 37°C
+'''Results:'''
+* cellgrowth ?
+</div>
+<div class="receptor">
+===Reamplifiying Streptactin from GSY6===
+'''Investigator: Christoph'''
+'''Aim:''' Reamplifiying Streptactin from GSY6 for further processing in QC reaction (delete NdeI site from pASK)
+'''Procedure:'''
+* PCR reaction was prepared according to SOP
+* Cycling steps were taken from the QC protocol because no further cycler was free
+'''Results:'''
+* will be available after DpnI digestion and transformation
+</div>
+<div class="polymerization">
+=== QuickChange-PCR of pASK75 with O29 and O30 ===
+'''Investigator: Christoph'''
+'''Aim:''' Deleting NdeI from pASK (P10)
+'''Procedure:'''
+* QC-PCR was performed according to SOP
+* Primers: O-029 and O-030
+* Annealing at 55°C
+* Elongation time: 5 min
+* 2-step protocol was applied
+</div>
+<div class="receptor">
+===Miniprep of E. coli Xl1-Blue P171, P172 and P173 (pSB1C3(CMV-BM40-Nanoluc-StrepTag-polyA)) ===
+'''Investigator: Javier'''
+'''Aim of the experiment:''' Extracting P171, P172 and P173 (CMV-BM40-Nanoluc-StrepTag-polyA) from E.coli XL-1-blue
+'''Procedure:'''
+* Miniprep was performed after manufacturer's protocol (QIAprep Miniprep, QIAGEN)
+* Concentrations:
+<table cellspacing="0" border="1">
+<tr>
+<td><b>Plasmid</b>
+</td><td><b>c [ng/µl]</b>
+</td></tr>
+<tr>
+<td>P171
+</td><td>75,4
+</td></tr>
+<tr>
+<td>P172
+</td><td>108,2
+<tr>
+<td>P173
+</td><td>66,4
+</td></tr></table>
+</div>
+<div class="receptor">
+=== Transformation of F136 (A3C5+Middle-Linker), F137 (EGFR+mRuby-Strep), F138 (mRuby3-Strep+PolyA) and P161 (QC mRuby-Strep) ===
+'''Investigator: Javier'''
+'''Aim of the experiment:''' Transformation of A3C5+Middle-Linker (F136), EGFR+mRuby-Strep (F137), mRuby3-Strep+PolyA (F138) and QC mRuby-Strep (P161) XL1 blue
+'''Procedure:'''
+transformation in competent E. coli XL1 blue according to protocol + rescue
+'''Result:'''
+plates (LB Cam) in incubator for further processing (37 °C)
+</div>
+<div class="receptor">
+===Colony PCR of F127 (CMV-BM40-Nanoluc-StrepTag-polyA)===
+'''Investigator: Clemens'''
+'''Aim:''' See if cloning was successfull
+'''Procedure:'''
+* samples wwere prepared with 5 µL Q5-Mastermix, 1 µl VF2-, 1 µL VR-Primer, 2 µL ddH20
+* six clones were picked and added to the samples respectively
+* PCR- cycles according to SOP (Annealing-temp: 66°C; Ampflification time: 1.5min)
+'''Results:'''
+* Lane 1: 1 kb Ladder
+* Lane 2: F127 K1
+* Lane 3: F127 K2
+* Lane 4: F127 K3
+* Lane 5: F127 K4
+* Lane 6: F127 K5
+* Lane 7: F127 K6
+[[File:Muc16_ColonyPCR_F117_1907.jpeg|500px]]
+</div>
+<div class="receptor">
+===Preparative digestion of P161 (pSB1C3(mRuby3-StrepTag)), P73 (pSB1C3((PolyA)), P96 ((pSB1C3(EGFR-TMD)), P69 (pSB1C3(Middle-linker)) and P112 (pSB1C3(A3C5)) ===
+'''Investigator: Clemens, Christoph, Javier'''
+'''Aim:''' Create biobricks
+'''Procedure:'''
+* Preparative digestion of P161 and P73
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl/ 20&nbsp;µl
+|Plasmid DNA P161/ P73
+|-
+|3&nbsp;µl/ 3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|EcoRI/ EcoRI
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|SpeI/ XbaI
+|-
+|10&nbsp;µl/ 5&nbsp;µl
+|ddH2O/ ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Preparative digestion of P96 and P161
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl/ 15&nbsp;µl
+|Plasmid DNA P96/ P161
+|-
+|3&nbsp;µl/ 3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|PstI/ PstI
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|AgeI/ NgOMIV
+|-
+|15&nbsp;µl/ 10&nbsp;µl
+|ddH2O/ ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Preparative digestion of P69 and P112
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|20&nbsp;µl/ 15&nbsp;µl
+|Plasmid DNA P69/ P112
+|-
+|3&nbsp;µl/ 3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|EcoRI/ EcoRI
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|AgeI/ NgOMIV
+|-
+|5&nbsp;µl/ 10&nbsp;µl
+|ddH2O/ ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated at 37°C for 2h
+* Samples were applied to a 1% agarose gel (40 min; 90V)
+* Samples were cut from the gel afterwards:
+* Renamed:
+** digest P69: F128
+** digest P112: F129
+** digest P161: F130
+** digest P96: F131
+** digest P161: F132
+** digest P73: F133
+'''Results:'''
+Fotos
+'''Procedure:'''
+* Gelextraction was performed after manufacturers protocol (Qiagen)
+* After gelextraction concentrations were measured:
+* Ligation:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|xx&nbsp;µl
+|Vektor F129
+|-
+|xx&nbsp;µl
+|Insert F128
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|x&nbsp;µl
+|ddH<sub>2</sub>O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|xx&nbsp;µl
+|Vektor F131
+|-
+|7xx&nbsp;µl
+|Insert F130
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|x&nbsp;µl
+|ddH<sub>2</sub>O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|xx&nbsp;µl
+|Vektor F133
+|-
+|7xx&nbsp;µl
+|Insert F132
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|x&nbsp;µl
+|ddH<sub>2</sub>O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* Ligation was performed according to SOP
+* Xl1 blue cells were transformed with the Ligations according to SOP
+</div>
+=='''Wednesday, July 20'''==
+<div class="general">
+===Analytical digestion and gelelectrophoresis of P171-P173 & QC of P10 ===
+'''Investigator: JB, MT'''
+'''Aim of experiment:'''  Check if everything is fine.
+'''Procedure:'''
+* Digest P171-P173 with XbaI + SpeI and QC of P10 with NedI and incubate 1 h at 37 °C
+* Run 1 % agarose-gel at least 40 min at 100 V
+'''Results:'''
+[[File:Muc16_digestion_P171_P172_P173_QCP10.jpeg|500px]]
+Lane1: 1Kb ladder; Lane2: P171; Lane3: P172; Lane4: P173; Lane5: QC of P10
+=> P171 was sent for sequencing: FR12904466
+=> NdeI test digestion shows two signals although there should have been just one
+</div>
+<div class="general">
+=== Preparation of GSY 6; F134; F135 for ligation===
+'''Investigator: JB, MT '''
+'''Aim of experiment:''' Prepare GSY6 for Ligation.
+'''Procedure:'''
+* Digestion of GSY6 with SpeI + HindIII
+* Preparative 1 % Agarose gel 100 V for at least 40 min.
+* Gel extraction of GSY6, F134, F135 by Quiagen kit.
+'''Results:'''
+* GSY6 -> F139 : 2.5 ng/µL
+* F134 : 4 ng/µL
+* F135 : 10.2 ng/µL
+Preparative agarose gel GSY6:
+[[File:Muc16_digestion_prep_gel_GSY6.jpeg|300px]]
+</div>
+<div class="general">
+===Ligation & transformation of F134 + F63; F135 + F139 ===
+'''Investigator: JB, MT'''
+'''Aim of experiment:'''  Ligation & transformation of F134 + F63; F135 + F139
+'''Procedure:'''
+Ligation following SOP(13.02.2013)
+* F134 + F63 -> F140
+* F135 + F139 -> F141
+transformation following SOP(13.02.2013)
+* F140 on CAM
+* F141 on AMP
+'''Results:'''
+   We will see tomorrow, please update this section.
+</div>
+=='''Thursday, July 21'''==
+<div class="receptor">
+=== Miniprep of F136 (K1 & K2) (pSB1C3(Middle linker-A3C5)), F137 (K1 & K2) (pSB1C3(EGFR TMD-mRuby3-StepTag)), F138 (K1 & K2) (pSB1C3(mRuby3-StrepTag-polyA) and retrafo of P161 (pSB1C3(mRuby3-StrepTag)) ===
+'''Investigator: Clemens'''
+'''Aim of experiment:'''  Get plasmids for analytical digestion and sequencing
+'''Procedure:'''
+* Minipreps were performed according to manufacturers protocol (Qiagen, QiaPrep)
+* Samples were renamed afterwards:
+** F136 K1: P174
+** F136 K2: P175
+** F137 K1: P176
+** F137 K2: P177
+** F138 K1: P178
+** F138 K2: P179
+** retrafo of P161: P180
+* Analytical digestion:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl
+|Plasmid DNA
+|-
+|1&nbsp;µl
+|Cutsmart (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI
+|-
+|0.5&nbsp;µl
+|PstI
+|-
+|7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Ligation was renamed: F143
+* Digestion products were seperated via gelelectrophoresis
+'''Results:'''
+Foto:
+* All plasmids seemed to carry the appropriate insert
+Sequencing:
+** P175: FR12904465 (VF2)
+** P177: FR12904464 (VF2)
+** P178: FR12904463 (VF2)
+</div>
+<div class="receptor">
+=== Preparative digestion of P116 (pSB1C3(IgKappa)) ===
+'''Investigator: Clemens, Christoph'''
+'''Aim of experiment:'''  cloning of CMV in front of IgKappa signal peptide
+'''Procedure:'''
+* preparative digestion batch
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl
+|Plasmid DNA P116
+|-
+|3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl
+|EcoRI
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|15&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestion was applied to a 1% agarose gel (45 min; 90V)
+* Sample was cut from the gel and gelextraction was performed according to manufacturers protocol
+* Ligation of Fx and F115 (digest CMV promotor):
+* Ligation:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3.9&nbsp;µl
+|Vektor F142
+|-
+|6.1&nbsp;µl
+|Insert F115
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|20&nbsp;µl
+|ddH<sub>2</sub>O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* Transformation of XL1blue was performed according to SOP
+* Cells were plated on LB medium (CAM) and incubated over night at 37°C
+</div>
+=='''Friday, July 22'''==
+<div class="streptavidin">
+=== Analytical digestion of pASK_T7 RBS_LCN2_His===
+'''Investigator: Luisa'''
+'''Aim of the experiment: '''
+Analytical digestion to find out whether there is more than one NdeI restriction site.
+'''Procedure:'''
+* Analytical digestion:
+**The plasmid was digested with NdeI and HindIII
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3&nbsp;µl
+|Plasmid DNA
+|-
+|1&nbsp;µl
+|Cutsmart (10x)
+|-
+|0.5&nbsp;µl
+|NdeI
+|-
+|0.5&nbsp;µl
+|HindIII
+|-
+|5&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+* Two bands were visible what means that there is only one NdeI restriction site.
+</div>
+<div class="receptor">
+===Inoculation of Precultures of F143 (pSB1C3(CMV+IgKappa))===
+'''Investigator: Luisa'''
+'''Aim:''' Prepare cells for miniprep of plasmids
+'''Procedure:'''
+* two colonies were picked and inoculated in LB medium (CAM)
+* Plates were incubated on a shaker at 37°C over night.
+</div>
+<div class="streptavidin">
+===Harvesting of Streptavidin===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Recombinant expression and purification of streptavidin
+'''Procedure:'''
+* the solution was spun down in the centrifuge (4°C, 15000 rpm, 20 mins) to remove last contamination
+* The pellet was discarded and the supernantant was dialysed against 20 mM Tris/HCl (ph 8) witt 50 mM NaCl
+* last step to do: steril filtration
+* the concentration was determined via UV/VIS: the absorption at 280 nm is 0.469 (1:100 dilution), this equals a concentration of 62 mg/mL (about 16 mL) (mass 54 kDa; Absorbtion coefficient 40455 1/M*cm
+</div>
+<div class="receptor">
+=== Sequencing of P174(Middle Linker + A3C5) ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* Sequencing batch were prepared after manufacturer's protocol. (15&nbsp;µl of plasmid DNA (50 - 100&nbsp;ng) and 2&nbsp;µl sequencing primer)
+</div>
+<div class="receptor">
+=== Cloning of P178 (mRubyStrepPolyA) / P180 (mRubyStrep) behind EGFR-TMD in pSB1C3 (P96) ===
+'''Investigator: Niklas'''
+'''Procedure:'''
+* Preparative digestion:
+* The Inserts were digested with PstI and NgoMIV
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|7.7 / 8.2&nbsp;µl (about 3µg)
+|Plasmid DNA
+|-
+|2&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl
+|PstI
+|-
+|1&nbsp;µl
+|NgoMIV
+|-
+|8.3 / 7.8&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* both fragments were ligated with F131 (digest P96 [AgeI; PstI])
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were taken out of stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 750&nbsp;µl LB-medium to each tube.
+* Incubation for 1 hour at 37&nbsp;°C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the cell-culture shaker.
+* Results: Cloning didn't work. No colonies on plate. Repeat.
+</div>
+<div class:"receptor">
+<div class="receptor">
+=== Cloning of Middle Linker before A3C5 in pSB1C3 (Repeat)===
+'''Investigator: Julian, Niklas'''
+'''Procedure:'''
+* Preparative digestion:
+**The Middle Linker (P69) was digested with EcoRI and AgeI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|30&nbsp;µl
+|Plasmid DNA
+|-
+|5&nbsp;µl
+|Cutsmart (10x)
+|-
+|1.5&nbsp;µl
+|EcoRI
+|-
+|1.5&nbsp;µl
+|AgeI
+|-
+|12&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+* the fragment was ligated with F129(digest P112 [EcoRI; NgOMIV])
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were taken out of stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 750&nbsp;µl LB-medium to each tube.
+* Incubation for 1 hour at 37&nbsp;°C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the cell-culture shaker.
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 11, July 25th - July 31st=
+<div class="week" id="Week_11">
+=='''Monday, July 25'''==
+<div class="receptor">
+===Inoculation of Precultures of F143 (pSB1C3(CMV+IgKappa)), F141new (pASK(Streptactin)), F151 (pSB1C3(middleLinker+A3C5), pASK75_T7-RBS-LCN2-His, F148 (pSB1C3(mRubyStrepPolyA+ CMV-EGFR Signal-Pept)===
+'''Investigator: Luisa'''
+'''Aim:''' Prepare cells for miniprep of plasmids
+'''Procedure:'''
+* Three colonies of each were picked and inoculated in LB medium (CAM) respectively (AMP) fpr pASK.
+* Plates were incubated on a shaker at 37°C for 6 hours.
+</div>
+<div class="receptor">
+===MiniPreps and analytical digestion of F143 cultures===
+'''Investigator: Luisa'''
+'''Aim:''' Prep plasmid DNA of F143 (pSB1C3(CMV + IgKappa)) and checking wheather ligation was successful.
+'''Procedure:'''
+* MiniPrep performed according to manufacturer's instructions with Qiagen kit
+* Prior to eluting, 30&nbsp;&mu;L EB buffer was applied to the membrane since the pellet was quite small, and the columns were heated at 37&nbsp;°C for 7&nbsp;min
+'''Results:'''
+* Concentrations: K1 = 230,4ng/µl, K2 = 162,4 ng/µl
+'''Analytical Digestion:'''
+* An 20µl batch was prepared for analytical digestion for each of the two clones:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl
+|Plasmid DNA
+|-
+|2&nbsp;µl
+|Cutsmart (10x)
+|-
+|1&nbsp;µl
+|EcoI
+|-
+|1&nbsp;µl
+|PstI
+|-
+|6&nbsp;µl
+|ddH2O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+* Two bands were visible at 750 Bp which is the size of IgKappa and CMV together. Cloning was successful. Sequence still has to be ckecked though.
+</div>
+<div class="receptor">
+=== Cloning of P178 (mRubyStrepPolyA) / P180 (mRubyStrep) behind EGFR-TMD in pSB1C3 (P96). Repetition. ===
+'''Investigator: Luisa'''
+'''Aim:''' See title.
+'''Procedure:'''
+*Digestion of P178 and P180: 7µg of DNA were digested.
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|18&nbsp;µl
+|Plasmid DNA
+|-
+|5&nbsp;µl
+|Cutsmart (10x)
+|-
+|2,5&nbsp;µl
+|NgoMIV
+|-
+|2,5&nbsp;µl
+|PstI
+|-
+|22&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestion at 37°C for 2,5h.
+</div>
+<div class="receptor">
+=== Cloning of NanoLuc-Strep-PolyA (F112) behind CMV-IgKappa in pSB1C3 (P181). ===
+'''Investigator: Luisa'''
+'''Aim:''' See title.
+'''Procedure:'''
+*Digestion of P181:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl
+|Plasmid DNA
+|-
+|5&nbsp;µl
+|Cutsmart (10x)
+|-
+|2,5&nbsp;µl
+|AgeI (20u/µl)
+|-
+|2,5&nbsp;µl
+|PstI (20u/µl)
+|-
+|30&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestion at 37°C for 2,5h.
+</div>
+<div class="general">
+=== Digestion and gel-extraction of P178; P180===
+'''Investigator: MT'''
+'''Aim of experiment:''' Preparation of P178 and P180 for ligation.
+'''Procedure:'''
+* Digest P178; P180 with NgoMIV + PstI incubate  1 h at 37 °C
+* Run 1 % agarose-gel at least 40 min at 100 V
+* Gel extraction by Quiagen kit.
+'''Results:'''
+* P178 [NgoMIV +PstI digest] -> F152: 17 ng/µL
+* P180 [NgoMIV +PstI digest] -> F153: 8.1 ng/µL
+[[File:Muc16_digestion_prep_gel_P178_P180.jpeg|300px]]
+</div>
+<div class="general">
+=== Ligation & transformation of F131 + F152; F131 + F153 ===
+'''Investigator: MT'''
+'''Aim of experiment:''' Ligation & transformation of F131 + F152; F131 + F153
+'''Procedure:'''
+Ligation following SOP(13.02.2013)
+* F131 + F152 -> F154
+* F131 + F153 -> F155
+Transformation following SOP(13.02.2013)
+* F154 E. coli. turbo CAM
+* F155 E. coli. turbo CAM
+'''Results:'''
+   We will see tomorrow, please update this section.
+</div>
+=='''Wednesday, July 27th'''==
+<div class="receptor">
+=== Minipreps of EGFR-TMD - mRuby - Strep - PolyA (F131+F152) and EGFR-TMD - mRuby - Strep (F131+F153)  ===
+'''Investigator: JB'''
+'''Results:'''
+Procedure according to protocol (spin kit). Resulting plasmids:
+EGFR-TMD - mRuby - Strep - PolyA (F131+F152) -> P196, P197
+EGFR-TMD - mRuby - Strep (F131+F153) -> P198, P199
+Concentrations:
+P196: 228 ng/µl
+P197: 212 ng/µl
+P198: 197 ng/µl
+P199: 322 ng/µl
+</div>
+=='''Thursday, July 28th'''==
+<div class="streptavidin">
+===Inoculation of Precultures of F141new (pASK(Streptactin))===
+'''Investigator: Luisa'''
+'''Aim:''' Prepare cells for miniprep of plasmids
+'''Procedure:'''
+* Three colonies of each were picked and inoculated in LB medium (CAM) respectively (AMP) fpr pASK.
+* Plates were incubated on a shaker at 37°C for 6 hours.
+</div>
+<div class="streptavidin">
+==='''PCR of GSY6'''===
+'''Investigator: Luisa'''
+'''Aim:''' Amplification of Streptavidin mutant and Traptactin for further cloning into pASK.
+'''Procedure:'''
+*reaction was performed after SOP (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
+* 2ng Plasmid were used for amplification (1 µL)
+* Primers: VR and VF2
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial Denaturation||98||30
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|66||30
+|-
+|72||90
+|-
+|final Extension||72||5
+|-
+|Hold||4||ꝏ
+|}
+* PCR product was purified accoding to manufacturer's protocol (PCR puification kit, Qiagen)
+* DNA was eluted 40 µL EB buffer
+</div>
+<div class="streptavidin">
+=== Digestion of pASK ===
+'''Investigator: Luisa'''
+'''Aim:''' Preparing pASK for ligation with Streptavidin mutant and Traptactin.
+'''Procedure:'''
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|20&nbsp;µl
+|Plasmid DNA
+|-
+|5&nbsp;µl
+|Cutsmart (10x)
+|-
+|1,5&nbsp;µl
+|NdeI
+|-
+|1,5&nbsp;µl
+|HindIII
+|-
+|22&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+</div>
+<div class="streptavidin">
+=== Cloning of Traptactin and Streptavidin mutant into pASK (P191). ===
+'''Investigator: Luisa'''
+'''Aim''': Preperation of the plasmids for Streptavidin and Traptactin expression in E.coli.
+'''Procedure''':
+* Cutting out the crucial bands from the gel containing the PCR-product and the digested plasmid (P190) and purifiing them with the Gelextraction Kit according to the protocoll. '''First Gel failed: Very small band with wrong length...--> Repetition of digestion with P190.'''
+* The PCR product of GSY6 was extracted from the gel (Band at ~800 Bp) with the Gelextraction Kit and then digested with NdeI and HindIII to get the fragments Streptavidin m1 and Traptactin. Inactivation was performed at 80°C for 10 min.
+* Concentrations: 33,9ng/µl (GSY6),
+* Ligation...
+</div>
+<div class="receptor">
+=== Cloning of NanoLuc-Strep-PolyA (F112) behind CMV-IgKappa in pSB1C3 (P182). Repetition. ===
+'''Investigator: JB'''
+'''Aim:''' See title.
+'''Procedure:'''
+*Digestion of P182:
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA
+|-
+|3&nbsp;µl
+|Cutsmart (10x)
+|-
+|1,5&nbsp;µl
+|AgeI (20u/µl)
+|-
+|1,5&nbsp;µl
+|PstI (20u/µl)
+|-
+|9&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestion at 37°C for 2.5h.
+* Take care: P182 is not sequenced
+</div>
+<div class="receptor">
+===Retrafos of P178 (mRuby-Strep-PolyA) and P181 (CMV + IgKappa)===
+'''Investigator: JB'''
+'''Results:'''
+Transformation according to protocol, plates were incubated at 37°C overnight.
+</div>
+<div class="polymerization">
+=== Dialysis of eGFP===
+'''Investigator: Julian'''
+'''Aim of the experiment:''' Preparation of eGFP for following biotinylation
+'''Procedure:'''
+* eGFP was poured in a dialysis hose (cut-off 14 kDa)
+* The hose was then placed in 4 L ice cold borate buffer 50 mM pH 8.85 (no salt)
+* The dialysis took place at 4°C over night
+</div>
+<div class="receptor">
+=== Sequencing of P160 (NanoLuc+StrepTag+Poly-A) ===
+'''Investigator: Julian'''
+'''Procedure:'''
+* Sequencing batch were prepared after manufacturer's protocol. (15&nbsp;µl of plasmid DNA (50 - 100&nbsp;ng) and 2&nbsp;µl sequencing primer)
+</div>
+=='''Friday, July 29th'''==
+<div class="receptor">
+=== Minipreps of EGFR-TMD - mRuby - Strep - PolyA (F131+F152) and EGFR-TMD - mRuby - Strep (F131+F153)  ===
+'''Investigator: Julian'''
+'''Procedure:'''
+Procedure according to protocol (spin kit). Resulting plasmids:
+CMV+EGFR-SigPep+mRuby3+StrepT+PolyA (F131+F152) -> P200, P201
+pASK_T7 RBS_LCN2_His (Vorlage für gewünschte Inserts) -> P202, P203
+'''Results:'''
+Concentrations:
+P196: 385.3 ng/µl
+P197: 462.6 ng/µl
+P198:  84.8 ng/µl
+P199:  96.0 ng/µl
+*Send for sequencing:
+**P201: FR12904454 (VF2)
+</div>
+<div class="streptavidin">
+=== Analytical digestion of P202 and P203 (pASK_T7 RBS_LCN2_His)===
+'''Investigator: Julian'''
+'''Aim of the experiment: '''
+Controll whether there is more than one NdeI restriction site.
+'''Procedure:'''
+* Analytical digestion:
+**The plasmid was digested with NdeI and HindIII
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2&nbsp;µl
+|Plasmid DNA
+|-
+|1&nbsp;µl
+|CutSmart buffer
+|-
+|0.5&nbsp;µl
+|NdeI
+|-
+|0.5&nbsp;µl
+|HindIII
+|-
+|6&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+* Two bands were visible what means that there is only one NdeI restriction site.
+</div>
+<div class="polymerization">
+=== Chemical biotinylation of BSA and eGFP===
+'''Investigator: Julian'''
+'''Procedure:'''
+g BSA was chemically biotinylated with a 40x molar excess of biotin-NHS-ester:
+* 100 ml of 50 mM borate buffer with 50 mM NaCl pH 8.85
+* dissolve BSA (10 mg/ml)
+* add adequate amount of biotin-NHS-ester: 205 mg
+* reaction for approx. 45 minutes at RT after full dissolving of biotin-NHS-ester
+* store at 4 °C
+eGFP was chemically biotinylated with a 16x (error in calculations) molar excess of biotin-NHS-ester:
+* eGFP in 75 ml of 50 mM borate buffer without NaCl pH 8.85
+* 1to10 dilution: extinction(280) = 0.371
+* add adequate amount of biotin-NHS-ester: 69 mg
+* reaction for approx. 45 minutes at RT after full dissolving of biotin-NHS-ester
+* store at 4 °C
+'''Next Steps'''
+* add another 104 mg of biotin-NHS-ester incl. reaction at RT tp reach desired 40X molar excess
+* Purification via column chromatography
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 12, August 1st - August 7th=
+<div class="week" id="Week_12">
+=='''Monday, August 01'''==
+<div class="streptavidin">
+===Cloning of Streptavidin/Streptactin/Traptactin from GSY5 and GSY6 into pASK75 + Transformation ===
+'''Investigator: JB'''
+*PCR products from GSY5 and GSY6 were, after digestion overnight with Nde1, loaded on an 1.8% agarose gel. The fragment bands at roughly 350 bps were extracted.
+*Digested pASK75 (P202 and P203 dig. with Nde1) were loaded onto an 1% agarose gel, the vector fragments at 3800 bp isolated and purified.
+*Vector fragment plus Streptavidin fragments were ligated and transformed into XL-1 blue
+-> F159+F160, F159+F161
+</div>
+<div class="receptor">
+===Cloning of EGFR-TMD - mRuby - Strep with IRES-BirA===
+'''Investigator: JB'''
+* 2 µg of P77 (EcoRI, XbaI) and P199 (EcoRI, SpeI) were digested for 2 hours at 37°C
+* Digestions were separated on a 1% agarose gel, fragments corresponding to the vector (P77) and to the to be cloned insert (P199) were isolated and purified
+* Ligation of inserts for 30 mins at RT
+* Transformation of ligation into XL1-blue
+</div>
+<div class="receptor">
+===Retrafos of cell culture constructs for signal peptide testing for midipreps ===
+'''Investigator: JB'''
+* Retransformation of all constructs in XL1-blue
+* Constructs concerned are: P152, P171, P205 (Nanoluc-constructs) and P201, P208 and P211 (mRuby-constructs)
+* Transformation according to protocol, plates incubated at 37°C overnight
+</div>
+=='''Tuesday, August 02'''==
+=='''Wednesday, August 03'''==
+<div class="receptor">
+=== Verification of cloning P210 (CMV-IgKappa-Nanoluc-StrepTag-PolyA) ===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Verification of successful cloning after sequencing showed that the last part of the construct might be missing
+'''Procedure:'''
+* digestion with AgeI and PstI (sample was digested with EcoRI and PstI for 10 minutes, than inactivated an ligated)
+'''Results:'''
+[[File:Muc16CMVIGKappaNanoluc.jpg|500px|]]
+* the gel shows a band at about 3500 bp (pSB1C3 + full insert)
+* gel shows additionally a band below 750 bp (CMV+ IgKappa)
+* the sample contains the full insert as well as the small insert (CMV+IgKappa without Nanoluc-StrepTag-PolyA)
+* cloning not succesful
+* the construct was inocculated from plate again
+</div>
+<div class="streptavidin">
+===  Transformation of ''E.&nbsp;coli'' XL1 blue with Ligations F159 + F160 and F159 + F161 (pASK + streptavidin from GSY 5 and 6)===
+'''Investigator: Niklas'''
+'''Aim of the experiment:''' Transformation of ''E.&nbsp;coli'' XL1 blue.
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cell suspension was plated on ampicillin plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the incubator.
+</div>
+=='''Thursday, August 04'''==
+<div class="general">
+=== MidiPrep P152 and P171 (pSB1C3) ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' isolate Plasmids
+'''Procedure:'''
+* MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen). After washing the DNA with 70% Ethanol the pellet was left in special centrifugation tubes (labeled 152+QF; 171+QF) in order to air-dry. EB buffer for storage was later added by CG.
+* Conc: 1000 ng/ul
+</div>
+<div class="receptor">
+=== Cloning of BAP Nanoluc (P206) before A3C5 (P213) ===
+'''Investigator: NA'''
+'''Procedure:'''
+* Preparative digestion:
+P213 (A3C5): EcoRI and NgoMIV -> F170
+P206 (BAP Nanoluc): EcoRI and AgeI -> F171
+Both fragments were ligated after gelextraction.
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were taken out of stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of Ligation was added to 100&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 750&nbsp;µl LB-medium to each tube.
+* Incubation for 1 hour at 37&nbsp;°C
+* The cell suspension was plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C in the cell-culture shaker.
+'''results:'''
+Gelextraction:
+[[File:Muc16BAPNanolucA3C5.jpg|500px]]
+the plates showed no colonies. repeat
+</div>
+=='''Friday, August 05'''==
+<div class="streptavidin">
+=== Verification of successful cloning of all Streptavidin variants into pASK75 ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Minipreps von pASK75 Streptavidin variants (codon optimzied Streptavidin, Streptactin, Traptactin)
+'''Procedure:'''
+* MiniPrep was performed according to the manufacturer's protocol (QIAprep MiniPrep, Qiagen) for 3 clones of GSY5 and 6 clones of GSY6
+* Analytic digestion with 0.25 ''µ''L NdeI, 0.25 ''µ''L HindII, 1 ''µ''L SmartCut Buffer, 200 ng plasmid DNA,  H<sub>2</sub>O to 20 µl
+* 10 ''µ''L on 1% agarose gel electrophoresis
+'''Results:''' Successful cloning was verified for all plasmids by analytical digestion. Expected and observed fragment size for the vector was 3.1 kb and about 350 bp for the inserts. 4 plasmids were sent for sequencing (1x GSY5, 3x GSY6). Alle sequences were error-free. Therefore all 3 Streptavidin variants are available now.
+</div>
+<div class="general">
+===  Transformation of: Streptavidin variants, PAS-Plasmid, Interlab-Plasmids, Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA and Ligation of BAP-Nanoluc-A3C5===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Transformation of  Streptavidin variants, PAS-Plasmid, Interlab-Plasmids into E. coli BL21 and Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA, Ligation of BAP-Nanoluc-A3C5 in E. coli XL1 blue
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of Ligations mixes were added to 50&nbsp;µl of competent cells and gently mixed, 1 µl for ccc Plasmids
+* 30&nbsp;min incubation on ice
+* 1 min. heat shock at 42&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube, and incubation for 1 h at 37°C
+* The cell suspension was plated on ampicillin plates (inclusive rescue plate) / CamR- plates and incubated for 7 h at 37&nbsp;°C in the programmed incubator.
+</div>
+<div class="receptor">
+===  Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA and Ligation of BAP-Nanoluc-A3C5===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Re-Ligation of EGFR-TMD-mRuby-Stre-IRES-BirA, Re-Ligation of BAP-Nanoluc-A3C5
+'''Procedure:'''
+The corresponding Fragments were mixed with 2 µl Ligase-buffer, 1 µl T4-Ligase and filled with water up to 20 µl
+* 7.3 µl F163 + 2.7 µl F162 (=F173)
+* 3.7 µl F170  + 6.3 µl F171 (=F174)
+The Ligation mixes were incubated for 1 h at room temperature.
+</div>
+<div class="streptavidin">
+=== SDS Page of Streptavidin production ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Verification of successful Streptavidin production and preperation for the data package
+'''Procedure:'''
+Streptavidin samples from the production process were further processed with SDS buffer. Some samples had very few volume, therefore the overall volume was reduced. For informations on the samples content please refer to NA. The low volume might be a problem due to evaporation issues.
+* Sample 1: the tube was empty
+* Sample 2: 1 µl sample was mixed with 7 µl water and 2 µl SDS buffer
+* Sample 3: 80 µl sample was mixed with 20 µl SDS buffer
+* Sample 4: 80 µl sample was mixed with 20 µl SDS buffer
+* Sample 5: 20 µl sample was mixed with 5 µl SDS buffer
+* Sample 6: 80 µl sample was mixed with 20 µl SDS buffer
+* Sample 7: 80 µl sample was mixed with 20 µl SDS buffer
+* Sample 8: 80 µl sample was mixed with 20 µl SDS buffer
+* Sample 9: 80 µl sample was mixed with 20 µl SDS buffer
+µl of each sample were loaded on the pre-mixed SDS gel.
+Gel 1: 8 µl Ladder, samples 1-6
+Gel 2: 8 µl Ladder, samples 7-9, 5 µl of samples 7-9
+The gel ran at 160 V for about 1 1/2 h. Afterwards it was incubated for 30 min. in staining solution, 10 min. in destaining solution 1 and over the weekend in destaining solution 2.
+'''Results:'''
+[[File:Muc16SDSstrep2.jpg|500px]]
+[[File:Muc16SDSstrep.jpg|500px]]
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 13, August 8th - August 14th=
+<div class="week" id="Week_13">
+=='''Monday, August 08'''==
+<div class="receptor">
+=== PCR, Purification and digestion of BirA ===
+'''Investigator: LK '''
+'''Aim of the experiment:''' Amplification of BirA
+'''Procedure:'''
+* PCR according to the SOP (primers: O17 and O18, Annealing at 62°C)
+* PCR purification via the purification kit according to the manufacturer's protocol
+* preparative digestion with XbaI and PstI over night in a 50µl batch
+'''Results:''''
+* Concentration after PCR-purification: 116ng/µl
+* Gel: One thick band at ~1000Bp --> BirA and one at ~2100Bp --> vector, we're cut out and purified via the Gelextraction kit according to the manufacturer's protocoll.
+* Concentrations: BirA (F186) : 62,5 ng/µl, pSB1C3 (F187): 32,5 ng/µl
+</div>
+<div class="streptavidin">
+=== Determination of Streptavidin concentration ===
+'''Investigator: NA '''
+'''Procedure:'''
+* OD280 measurement with quartz cuvette
+'''result:''' the 1:100 dilution showed an OD of 0,469
+Calculation with extinction coefficient (expasy tool) of 41940 M <sup>-1</sup> * cm <sup>-1</sup> and 13.3 kDA as molar mass of streptavidin monomer provides concentration below:
+.87 mg/mL
+</div>
+<div class="streptavidin">
+=== Inocculation of Streptavidin (wild type, P235) in M9 medium for fermentation ===
+'''Investigator: NA '''
+'''Procedure:'''
+* M9 medium with Amp (1:1000) is inocculated with preculture (~50 mL) of P235
+* the culture is incubated in the shaker over night at 37°C
+</div>
+<div class="receptor">
+<div class="receptor">
+=== PCR purification ===
+'''Investigator: EF '''
+'''Aim of the experiment:''' Purificate bands for blunt ligation in F113
+</div>
+<div class="hypoxia">
+=== Seeding of HEK293T cells in cell culture===
+'''Investigator: JB'''
+'''Aim of experiment:'''
+Thawing and seeeding of HEK293T cells for experiments later this week
+'''Procedure:'''
+* Tube with cells was thawed quickly in a 37°C waterbath
+* After bringing most of the cell suspension in a fluid state, the suspension was transferred into a 50 ml Falcon tube and suspended in 50 ml of RPMI1640 medium (with 10% CFS and Pen/Strep added).
+* Cells were spun down for 2 mins at 2,300 rcf and the pellet resuspended in 20 ml of medium in order to remove residual DSMO from the cells (DSMO having been used for freezing the cells).
+* The resuspended cells were transferred into a culture flask and incubated overnight at 37°C/5% CO².
+</div>
+<div class="general">
+=== Cloning of IgKappa signale peptide, PAS-Lysin and further constructs for the receptor===
+'''Investigator: CG'''
+'''Aim of experiment:'''
+Cloning of CMV-IgKappa+Nanoluc-Strep-PolyA, BAP-Nanoluc+A3C5, IRES-BirA + polyA and Sumo-PAS-Lysin into pASK75
+'''Procedure:'''
+Digestion of 3 µg of each plasmid in 30 µl mix:
+* 20 µl P205 (CMV-IgKappa) with EcoRI, AgeI -> Gel 1, left lane, expected fragment at about 600 bp -> F175
+* 15 µl P160 (Nanoluc-Strep-PolyA) with EcoRI, NgoMiV -> Gel 1, right lane, expected fragment at about 3000 bp -> F176
+* 20 µl P212 (A3C5) with EcoRI, NgoMiV -> Gel 2, left lane, expected fragment at about 2.200 bp -> F177
+* 10 µl P206 (BAP-Nanoluc) with EcoRI, AgeI -> Gel 2, right lane, expected fragment at about 500 bp -> F178
+* 10 µl P199 (EGFR-TMD-mRuby-Strep) with EcoRI, SpeI -> Gel 3, left lane, expected fragment at about 1.500 bp -> F179
+* 20 µl P236 (PAS-Lysin-Sumo) with NdeI, HindIII -> Gel 3, right lane, expected fragment at about 1.000 bp -> F180
+* 10 µl P77 (IRES-BirA-KDEL) with EcoRI, SpeI -> Gel 4, left lane, expected fragment at about 1000 bp -> F181
+Ligation in 20 µl mix (s. above fragment names):
+* F182: 2.9 µl F176 + 7.1 µl F175
+* F183: 5.2 F177 + 4.8. F178
+* F184: 7.0 µl F159 + 3.0 µl F180
+* F185: 2.9 µl F133 + 7.1 µl F181
+Transformation according to SOP.
+'''Results:'''
+For all ligations colonies grew the next day.
+Gel 1:
+[[File:Muc16_PrepDigest_160808_1.jpg|500px]]
+Gel 2:
+[[File:Muc16_PrepDigest_160808_2.jpg|500px]]
+Gel 3:
+[[File:Muc16_PrepDigest_160808_3.jpg|500px]]
+Gel 4:
+[[File:Muc16_PrepDigest_160808_4.jpg|500px]]
+</div>
+=='''Tuesday, August 09'''==
+<div class="receptor">
+=== Transformation of Biobricks in NEB Turbo ===
+'''Investigator: Julian'''
+'''Aim of the experiment:''' Acquisition of pBAD/AraC and Lox site
+'''Procedure:'''
+* resuspend DNA with 10 µl ddH2O in well of interest (standard distribution kit)
+* incubate for 5 min
+* transformation of 1 µl plasmid according to SOP in NEB Turbo
+Used bricks:
+BBa_I0500 and BBa_J61046
+</div>
+<div class="receptor">
+=== Inoculation and induction of AraC+pBAD controlled eGFP production in E.coli BL-21 ===
+'''Investigator: LK '''
+'''Aim of the experiment:''' Confirmation of arabinose dependend activation of the pBAD-promotor in AraC-Operon.
+'''Procedure:'''
+* E.coli Bl-21 with P61 (PC+AraC+pBAD+eGFP in pSB1C3) we're picked and a 4ml preculture (LB+cam) was inoculated and incubated for 6h.
+* According to the following table 50ml cultures (LB+cam) we're incoculated with 500µl of the preculture and incubated over night at 37°C.
+{|cellspacing="0" border="1"
+|'''Arabinose concentration:'''
+|negative control
+|100mM
+|10mM
+|1mM
+|100µM
+|10µM
+|}
+'''Results:'''
+</div>
+<div class="receptor">
+=== Cloning of F186 (BirA) into F187 (pSB1C3) ===
+'''Investigator: LK '''
+'''Aim of the experiment:''' Getting the BirA for the prokaryotic receptor.
+'''Procedure:'''
+* 1,7µl of F187 and 6,3µl of F186 we're ligated for 1h at RT accoridng to the SOP. --> F189
+* The ligation-batch was transformed into NEB-Turbo cells and plated out on cam-plates. Incubation at 37° o/n.
+</div>
+<div class="receptor">
+=== Inoculation of precultures from Ligations F182-F185 ===
+'''Investigator: LK '''
+'''Aim of the experiment:''' Getting plamids of CMV-IgKappa+Nanoluc-Strep-PolyA (F182), BAP-Nanoluc+A3C5 (F183),Sumo-PAS-Lysin (F184) and IRES-BirA + polyA (F185)
+'''Procedure:'''
+* Inoculation of 4mL cultures (LB cam resp. amp (F184)). Incubation at 37°C o/n.
+</div>
+<div class="streptavidin">
+=== Inocculation of fermenter ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* centrifuge preculture (P235 in M9 medium)
+* resuspend pellet in HCDF medium and inocculate fermenter (HCDF medium)
+* pO<sub>2</sub>= 60 %; Temp= 30°C, pH~7
+* growth over night
+</div>
+<div class="streptavidin">
+=== SDS Page of Streptavidin production ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Verification of successful Streptavidin production and preperation for the data package
+'''Procedure:'''
+Streptavidin samples from the production process were further processed with SDS buffer. Some samples had very few volume, therefore the overall volume was reduced.
+* 1: 8 µl Ladder
+* 2: 10 µl after induction (1 µl sample was mixed with 7 µl water and 2 µl SDS buffer)
+* 3: 5 µl supernantant after denaturation (20 µl sample was mixed with 20 µl H<sub>2</sub>O and 10 µl SDS buffer)
+* 4: 5 µl before precipitation(80 µl sample was mixed with 20 µl SDS buffer)
+* 5: 10 µl supernantant after 40% precipitation (80 µl sample was mixed with 20 µl SDS buffer)
+* 6: 10 µl supernantant after 70% precipitation (80 µl sample was mixed with 20 µl SDS buffer)
+* 7: 10 µl after dissolving in 2.2M (NH<sub>4</sub>)2SO<sub>4</sub> (80 µl sample was mixed with 20 µl SDS buffer)
+The gel ran at 145 V
+'''Results:'''
+[[File:Muc16sa31.jpg|500px]]
+</div>
+<div class="general">
+=== Transformation of F192 and P238 ===
+'''Investigator: NA'''
+'''Procedure:'''
+* CaCl2 competent ''E.&nbsp;coli'' XL1-Blue cells were put out from the stock in -80&nbsp;°C freezer and were gently thawed on ice.
+* 7&nbsp;µl of DNA was added to 50&nbsp;µl of competent cells and gently mixed.
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min. heat shock at 37&nbsp;°C
+* Adding of 950&nbsp;µl LB-medium to each tube.
+* The cell suspensions were plated on Cam-plates (inclusive rescue plate) and incubated over night at 37&nbsp;°C.
+</div>
+=='''Wednesday, August 10'''==
+<div class="receptor">
+=== Minipreps and analytical digestion of P237 - P243 ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Isolating and verifiing plamids of CMV-IgKappa+Nanoluc-Strep-PolyA (F182), BAP-Nanoluc+A3C5 (F183),Sumo-PAS-Lysin (F184) and IRES-BirA + polyA (F185)
+'''Procedure:'''
+* Minipreps were performed according to the manufacturer's protocol.
+* ~200- 500ng of ach Plasmid (accept P241) were digested with EcoI and PstI for 45 min. and a gel-elctrophoresis (1% Agarose) of the digestion-batches was performed.
+'''Results:'''
+ * P237: expected band for CMV-IgKappa+Nanoluc-Strep-PolyA at ~1850 Bp , but unexpected band at ~1100. Discard sample?
+ * P238: expected band for CMV-IgKappa+Nanoluc-Strep-PolyA at ~1850 Bp
+ * P239 and P240: expected band at ~650 Bp
+ * P242 and P243: bands at ~2000 Bp. Digested vector and Fragment are not distinguishable --> sequencing
+</div>
+<div class="receptor">
+=== Cloning constructs for the eukaryotic and prokaryotic receptor===
+'''Investigator: CG'''
+'''Aim of experiment:'''
+Cloning of EGFR-TMD-mRuby-Strep-IRES-BirA-KDEL-PolyA, BAP-Nanoluc-A3C5-EspP-2xTerm
+'''Procedure:'''
+Digestion of 3 µg of each plasmid in 30 µl mix:
+* 6 µl P242 (IRES-BirA-KDEL-PolyA) with EcoRI, XbaI -> Gel 1, left lane, expected fragment at about 4000 bp -> F190
+* 20 µl P108 (EspP-Termin.) with EcoRI, NgoMiV -> Gel 1, right lane, expected fragment at about 3000 bp -> F191
+Ligation in 20 µl mix (s. fragment names above):
+* F192: 4 µl F190 + 6 µl F179
+Transformation according to SOP.
+'''Results:'''
+Gel 1:
+[[File:Muc16_PrepDigest_160810_1.jpg|500px]]
+</div>
+<div class="hypoxia">
+=== Transformation of P22; P67; P122; P137; P160 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of P22; P67; P122; P137; P160
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|P22
+|K157001
+|RFP-Gen.(Retrafo P4)
+|-
+|P67
+|pSB1C3
+|EGFR signal peptide (transloc. pore)
+|-
+|P122
+|pSB1C3
+|Ig Kappa (digest. GSY3)
+|-
+|P137
+|pSB1C3
+|T7/BM40 aus GSY
+|-
+|P160
+|pSB1C3
+|NanoLuc + StrepTag + Poly-A
+|}
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="streptavidin">
+=== Fermentation ===
+'''Investigator:''' NA
+'''Aim of the experiment:''' Streptavidin production
+'''Procedure:'''
+* exponential feed (glucose, MgSO<sub>4</sub>, Thiamin, Amp, HCDF salt, micronutrients) for ~13 h (about 3-4 L)
+* Induction of streptavidin expression (anhydro tetracyclin) at OD= 111.2
+* production over night
+</div>
+=='''Thursday, August 11'''==
+<div class="receptor">
+=== Minipreps and analytical digestion of BBa_I0500 (AraC+ pBAD), BBa_J61046 (LoxP) and F189 (BirA) ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Isolating and verifiing the plasmids.
+'''Procedure:'''
+* The Preperation was performed according to the manufacturer's protocol.
+* Each plasmid was digested with EcoRI and PstI and a gel-elctrophoresis (1% Agarose) of the digestion-batches was performed.
+'''Results:'''
+* BBa_I0500 (AraC+ pBAD) = P246 and P247: Band at ~1250; Cloning was succesful
+* BBa_J61046 (LoxP) = P244 and P245: Fragment is too small (34Bp), not visible on gel.
+* F189 (BirA) = P248: Band at ~ 1000Bp; Cloning was succesful
+</div>
+<div class="streptavidin">
+=== Cloning of Streptavidin-variants into pASK111===
+'''Investigator: JB, LK, CG'''
+'''Aim of experiment:'''
+Cloning of Streptactin, Traptavidin, Streptavidin into CamR pASK111
+'''Procedure:'''
+Digestion of about 2.5 µg of each plasmid in 30 µl mix:
+* 25 µl P233 (Streptavidin) with XbaI, HindIII  -> Gel 1, left lane, expected fragment at about 400 bp -> F195
+* 25 µl P231 (Traptavidin) with XbaI, HindIII  -> Gel 1, right lane, expected fragment at about 400 bp -> F196
+* 15 µl P241 (PAS-Lysin) with XbaI, HindIII  -> Gel 2, left lane, expected fragment at about 400 bp -> -
+* 25 µl P229 (Streptactin) with XbaI, HindIII  -> Gel 2, left right, expected fragment at about 400 bp -> F197
+* 15 µl P249 (pASK111) with XbaI, HindIII -> Gel 3, left lane, expected fragment at about 3000 bp -> F198
+Ligation in 20 µl mix overnight (s. fragment names above):
+* F199: 3.7 µl F195 + 6.3 µl F198
+* F200: 5.4 µl F196 + 4.6 µl F198
+* F201: 4.1 µl F197+ 5.9 µl F198
+Transformation according to SOP.
+'''Results:'''
+Gel 1:
+[[File:Muc16_PrepDigest_160811_1.jpeg|500px]]
+Gel 2:
+[[File:Muc16_PrepDigest_160811_2.jpg|500px]]
+Gel 3:
+[[File:Muc16_PrepDigest_160811_3.jpg|500px]]
+</div>
+<div class="polymerization">
+===Testpolymerization: BSA-coating===
+'''Investigator: EU, JH'''
+'''Aim of experiment:'''
+Coating of 6-well plate with BSA according to a modified ELISA-protocol.
+'''Procedure:'''
+Bicarbonate/carbonate coating buffer (100mM):
+,3 mg Na2CO3
+mg NaHCO3
+ml distilled water
+"Blocking" Buffer:
+% BSA in PBS
+Each well was covered with 0,5 ml BSA buffer and 0,5 ml bicarbonate buffer. After overnight incubation at RT, solution in wells was aspirated one by one and streptavidin was added. After a short incubation, the streptavidin(&Tris/HCl) solution was aspirated and Biotin solution was added (by needle).
+. well: 200 µl Streptavidin (11,2 mg/ml) + 200 µl Biotin, 2. well: 400 µl Streptavidin and 400 µl Tris/HCl + 200 µl Biotin, 3. well: 500 µl Streptavidin and 500 µl Tris/HCl + 300 µl Biotin, 4. well: 500 µl Streptavidin + 10 µl Biotin (this time with 2,5 µl pipette)
+'''Results:'''
+Overall polymerization was observed again, although it seemed more like an aggregation than a polymerization.
+No coating was observed except in the 4. well. Biotin-injection speed may be the critical point.
+Poly-D-Lysine coating will follow as next step.
+</div>
+<div class="hypoxia">
+=== Transformation of P64; P73 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of P22; P67; P122; P137; P160
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|P64
+|pSB1C3
+|VEGF-p2a-PDGF
+|-
+|P73
+|pSB1C3
+|Poly-A
+|}
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of P22; P67; P122; P137; P160 ===
+'''Investigator: EF, MP '''
+'''Aim of the experiment:'''
+Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="streptavidin">
+=== harvesting streptavidin ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* OD= 174
+* centrifuge culture
+* freeze pellet
+</div>
+<div class="streptavidin">
+=== SDS PAGE Streptavidin fermentation ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Verification of successfull production
+'''Procedure:'''
+* according to protocol
+* 8 µl Ladder; before induction; after induction
+* both samples: 3 µl culture + 77 µl TB + 20 µl SDS buffer; 12 µl on SDS gel
+'''Results:'''
+[[File:Muc16FermentationVORNACH2.1.jpg|500px]]
+*The fermentation was not successful, streptavidin band (unter 15 kDa marker) is just a bit thicker. The reason might be the ampR of the transformed plasmid. Due to the high cell concentration beta lactamase (secreted in periplasma) gets in the medium and hydrolyses amp. As a result cells lose plasmid because there is no selective pressure without an antibiotic in medium.
+* next step: cloning pf streptavidin mutants into pASK111 (camR)
+</div>
+<div class="general">
+=== Sequencing of P238, P245, P248  ===
+'''Investigator: NA'''
+'''Procedure:'''
+* Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer) - all samples: VF2
+* barcodes in stock list
+</div>
+=='''Friday, August 12'''==
+<div class="hypoxia">
+=== PCR of Gensythesis (GSY) 7 and 8 ===
+'''Investigator: MT'''
+'''Aim of the experiment:'''
+Amplification of GSY 7 and 8
+'''Procedure:'''
+*PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''25 µL reaction'''
+|'''Final concentration'''
+|-
+|5X Q5 Reaction Buffer
+|5 µL
+|1 X
+|-
+|10 mM dNTPs
+|0.5 µL
+|200 μM
+|-
+|10 μM Forward Primer (D20)
+|1.25 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (VR)
+|1.25 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Q5 High-Fidelity DNA Polymerase
+|0.25 μl
+|0.02 U/μl
+|-
+|Nuclease-Free Water
+|to 25 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||5 - 10 sec
+|-
+|61 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|16 °C
+|-
+|}
+Note: Use of the NEB T m Calculator is highly recommended.
+'''Results:'''
+After running on 1 %agarose gel only the 2kb bands belonging to GSY8 could be distinguished. These were extracted from the gel.
+-> Repeat PCR for GSY7
+</div>
+<div class="hypoxia">
+===  Gelextraction of GSY8 ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' Gelextraction of 2kb band of PCR belonging to GSY8
+'''Procedure:'''
+Gelextraction was performed by manufacturers protocol (SLG).
+'''Concentration:'''
+,7 ng/ul
+</div>
+<div class="general">
+=== Plasmid preparation of liquid culture of P22; P67; P122; P137; P160 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of P22; P67; P122; P137; P160
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|P22
+|K157001
+|RFP-Gen.(Retrafo P4)
+|-
+|P67
+|pSB1C3
+|EGFR signal peptide (transloc. pore)
+|-
+|P122
+|pSB1C3
+|Ig Kappa (digest. GSY3)
+|-
+|P137
+|pSB1C3
+|T7/BM40 aus GSY
+|-
+|P160
+|pSB1C3
+|NanoLuc + StrepTag + Poly-A
+|}
+'''Procedure:'''
+* According to Mini-prep kit, SLG
+'''Results:'''
+* P22 ->P1001 103.6 ng/µL
+* P67 ->P1004 92.9 µL
+* P122 -> P1000 80.8 ng/µL
+* P137 -> P1003 87.9 µL
+* P160 -> P1002 100 ng/µL
+</div>
+<div class="hypoxia">
+=== Dephosphorylation of F113[HincII digested] ===
+'''Investigator: MP, EF '''
+'''Aim of the experiment:'''
+Dephosphorylation of F113[HincII digested] (RFP-Reportercassette )
+'''Procedure:'''
+According to NEB online Protocol for Dephosphorylation of 5 ́-ends of
+DNA using Antarctic Phosphatase (M0289):
+* 12 µL F113 (85.1 ng/µL)
+* 2 µL Antarctic Phosphatase Rxn Buffer (10X)
+* 1 µL Antarctic Phosphatase (5000 u/mL)
+* 5 µL ddH2O
+</div>
+<div class="receptor">
+=== Midiprep P238 (CMV-IgKappa-Nanoluc-Strep-polyA) ===
+'''Investigator: NA'''
+'''Procedure:'''
+* MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)
+'''Results:'''
+P253 - concentration: 2134 ng/µl
+</div>
+<div class="hypoxia">
+ === Digestion, Gel extraction and ligation of F1000 (P122), F1001 (P67), F1002 (P160) and F1003 (P137) ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+Preparation of plasmids
+'''Procedure:'''
+* 33 µL DNA
+* 1 µL enzyme 1
+* 1 µL enzyme 2
+* 5 µL cut smart buffer
+* 10 µL ddH20
+Enzymes used:
+* F1000: AgeI + PstI
+* F1001: AgeI + PstI
+* F1002: NgoMiT + PstI
+* F1003: AgeI + PstI
+Gelextraction:
+* Using gelextraction kit, Quiagen
+Ligation
+* 2µl F1000 + 6µl F1002
+* 2µl F1001 + 6µl F1002
+* 2µl F1003 + 6µl F1002
++ 1µl T4 Ligase and 1 l T4 ligase buffer for each ligation
+'''Results:''''
+Left to right F1002(2x), F1001(2x), F1000(2x) and F1003(1x)
+* F1000 30 ng/µL
+* F1001 23,8 ng/µL
+* F1002 9,4 ng/µL
+* F1003 23,1 ng/µL
+</div>
+=='''Saturday, August 13'''==
+<div class="linkers">
+=== Miniprep of pASK111 (empty) and diegestion ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Amplification of pASK111 and digestion for further ligation with SUMO-PAS-Lysin.
+'''Procedure:'''
+* The Miniprep was performed according to the manufacturer's protocol.
+* The whole DNA was diegested with XbaI and HindIII. Over night at 37°C.
+* Gelelectrophoresis was performed and showed a significant band at ~2700.
+'''Comment'''
+* Gel-ectraction has yet to be done .
+* equally digested insert from P236 was visible on gel. --> no ligation possible.
+</div>
+<div class="hypoxia">
+=== Transformation of F1006; F1007; F1008 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of F1006; F1007; F1008
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Ligation'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|F1006
+|F1000 + F1002
+|pSB1C3
+|Ig Kappa  + NanoLuc + StrepTag + Poly-A
+|-
+|F1007
+|F1003 + F1002
+|pSB1C3
+|T7/BM40 + NanoLuc + StrepTag + Poly-A
+|-
+|F1008
+|F1001 + F1002
+|pSB1C3
+|EGFR + NanoLuc + StrepTag + Poly-A
+|}
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="hypoxia">
+=== Digestion and gelextraction of P64; P73 ===
+'''Investigator: JB, MT '''
+'''Aim of the experiment:'''
+Preparation for ligation
+'''Procedure:'''
+* 10 µL DNA
+* 1 µL enzyme 1
+* 1 µL enzyme 2
+* 2 µL buffer
+* 6 µL ddH20
+Enzymes used:
+* P64: EcoRI + SpeI
+* P73: EcoRI + XbaI
+Gelextraction:
+* Using gelextraction kit, Quiagen
+'''Results:''''
+[[File:Muc16_digestion_P64_P73.png|250px]]
+Left: P64 Right: P73
+* P64 -> F1011 14,2 ng/µL
+* P73 -> F1012 17,6 ng/µL
+</div>
+=='''Sunday, August 14'''==
+<div class="streptavidin">
+===Miniprep of P199-P201 and analytical digestion ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Isolation of "Streptavidin-variants" in pASK111 for preinoculation tomorrow.
+'''Procedure:'''
+* The Miniprep was performed according to the manufacturer's protocol.
+* ~200ng where digested with XbaI and HindIII.
+'''Results:'''
+* All samples showed significant bands at ~400 Bp.
+</div>
+<div class="streptavidin">
+=== Transformation of P199-201 into E.coli BL-21===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Introducing Strep-variants in pASK111 into BL-21 for further fermentation.
+'''Procedure:'''
+* The cells were transformed according to the SOP with 1µl of DNA and after 1h of incubation in LB without antibiotics plated out on Cam-plates.
+</div>
+<div class="receptor">
+===Miniprep of P113-P213 and analytical digestion ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Isolation of "Streptavidin-variants" in pASK111 for preinoculation tomorrow.
+'''Procedure:'''
+* The Miniprep was performed according to the manufacturer's protocol.
+* ~200 ng were digested with EcoRI and PstI.
+'''Results:'''
+*
+</div>
+<div class="hypoxia">
+=== PCR of Gensynthesis (GSY) 7, 8  ===
+'''Investigator: MT'''
+'''Aim of the experiment:'''
+Amplification of GSY7
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491)
+* Different amounts of template DNA were used
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|5X Q5 Reaction Buffer
+|10 µL
+|1 X
+|-
+|10 mM dNTPs
+|1 µL
+|200 μM
+|-
+|10 μM Forward Primer (D20)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (VR)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|1 - 10 ng
+|-
+|Q5 High-Fidelity DNA Polymerase
+|0.5 μl
+|0.02 U/μl
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|40 cycles||98 °C||5 - 10 sec
+|-
+|58 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+'''Results:'''
+*PCR GSY8 successful.
+-> Do it again for GSY 7!
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of F1006; F1007; F1008 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="hypoxia">
+=== Gelextaction of F1004 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+'''Procedure:'''
+* Using gelextraction kit, Quiagen
+'''Results:''''
+[[File:Muc16_gelextraction_F1004.png|250px]]
+* long F1004 -> F1013 6,4 ng/µL
+* short F1004 -> F1014 1,1 ng/µL
+</div>
+<div class="hypoxia">
+=== Ligation F1012 + F1011 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Ligation F1012 + F1011
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmind'''
+|'''Description'''
+|-
+|F1011
+|
+|VEGF-p2a-PDGF
+|-
+|F1012
+|pSB1C3
+|Poly-A
+|}
+'''Procedure:'''
+* 3 µL F1012
+* 6 µL F1011
+* 2 µL buffer
+* 1 µL T4 Ligase
+* 8 µL ddH2O
+'''Results:'''
+* F1015
+</div>
+<div class="hypoxia">
+=== Transformation of F1015 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of F1015
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Ligation'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|F1015
+|F1011 + F1012
+|pSB1C3
+|VEGF-p2a-PDGF + poly-A
+|}
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+'''Results:'''
+* No colonies. Do it again.
+</div>
+<!--- this closes the week -->
+</div>
+<!--- ^^^^ this closes the week -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+<!--- PLEASE DO NOT TOUCH !!!! -->
+=Week 14, Aug 15th - Aug 21st=
+<div class="week" id="Week_14">
+=='''Monday, Aug 15th'''==
+<div class="receptor">
+=== Analytical digestion of P251 and P252 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Verify cloning
+'''Procedure:'''
+* 1µL Plasmid was digested with 1µL of EcoRI and PstI
+* Digestions were incubated for 1h
+* Samples were seperated by gelelectrophoresis on a 1% agarose gel
+'''Results:'''
+* Cloning seems to have worked
+[[File:Muc16_P251_P252.png|500px]]
+</div>
+<div class="hypoxia">
+=== Plasmidpreparation of liquid culture of F1006; F1007; F1008 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of F1006; F1007; F1008
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|F1006
+|pSB1C3
+|Ig Kappa  + NanoLuc + StrepTag + Poly-A
+|-
+|F1007
+|pSB1C3
+|T7/BM40 + NanoLuc + StrepTag + Poly-A
+|-
+|F1008
+|pSB1C3
+|EGFR + NanoLuc + StrepTag + Poly-A
+|}
+'''Procedure:'''
+* According to Mini-prep. kit, Quiagen
+'''Results:'''
+* F1006 -> F1005 83.2 ng/µL
+* F1007 ->  F1006 91.8 ng/µL
+* F1008 -> F1007 367.1 ng/µL
+</div>
+<div class="receptor">
+=== Cloning of Nanoluc-Strep in front of double terminator and PAS-Lysine into pASK111===
+'''Investigator: LK, CG'''
+'''Aim of experiment:'''
+Cloning of Nanoluc-Strep in front of double terminator and PAS-Lysine into pASK111
+'''Procedure:'''
+Plasmid preperation according to SOP of P264, P265
+Digestion of about 3 µg of each plasmid in 30 µl mix:
+* 6 µl P29 (double teminator) with EcoRI, XbaI  -> Gel 1, left lane, expected fragment at about 3000 bp -> F207
+* 15 µl P98 (Nanoluc-Strep) with EcoRI, SpeI  -> Gel 1, right lane, expected fragment at about 500 bp -> F208
+* 15 µl P264 (PAS-Lysin) with XbaI, HindIII  -> Gel 2, left lane, expected fragment at about 1000 bp -> F210
+Ligation in 20 µl mix for 30 min. at room temperature (s. fragment names above):
+* F209: 3.7 µl F207 + 6.3 µl F208
+* F211: 1.1 µl F210 + 8.9 µl F206
+Transformation according to SOP.
+'''Results:'''
+Gel 1:
+[[File:Muc16_PrepDigest_160816_1.jpeg|500px]]
+Gel 2:
+[[File:Muc16_PrepDigest_160816_2.jpeg|500px]]
+</div>
+=='''Tuesday, Aug 16th'''==
+<div class="hypoxia">
+=== Over night liquid culture of P64; P73 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="hypoxia">
+=== Gelextraction of PCR GSY8(Saturday, August 13) ===
+'''Investigator: EF '''
+'''Aim of the experiment:'''
+Purification of PCR GSY8(Sunday, August 14)
+'''Procedure:'''
+* Using gelextraction kit, SLG
+'''Results:'''
+* F1016 3,4 ng/µL
+</div>
+<div class="receptor">
+=== Seeding of HEK293T cells for transfection ===
+'''Investigator: LK, CG '''
+'''Aim of the experiment:'''
+x4 petri dishes with HEK293T cells for performing the Nanoluc assay in order to validate the signale peptides
+'''Procedure:'''
+* Washing each T75 flask with 10 ml PBS
+* Centrifugation for 10 min. at 1.8 rcf
+* Resuspending the cell pellet in 10 ml medium
+* Counting the cells (33x10^6 cells in 10 ml)
+* Plating 0.5x10^6 cells onto petri dishes in 10 ml medium an 1x10^6 onto a T75 flask
+* Incubation for 2 days
+'''Results:'''
+* ready to transfect cells in petri dishes
+</div>
+<div class="hypoxia">
+=== Gelextraction of PCR GSY8(Saturday, August 13) ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of PCR GSY8(Sunday, August 14)
+'''Procedure:'''
+* Using gelextraction kit, SLG
+'''Results:'''
+* F1016 3,4 ng/µL
+</div>
+<div class="hypoxia">
+=== Transformation of F1015 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of F1015
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Ligation'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|F1015
+|F1011 + F1012
+|pSB1C3
+|VEGF-p2a-PDGF + poly-A
+|}
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="hypoxia">
+=== PCR of Gensynthesis (GSY) 7  ===
+'''Investigator: EF'''
+'''Aim of the experiment:'''
+Amplification of GSY7
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491)
+* Reactions with and without GC Enhancer were performed
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction x 6'''
+|'''Final concentration'''
+|-*Product could not be purified
+|5X Q5 Reaction Buffer
+|10 µL
+|1 X
+|-
+|10 mM dNTPs
+|1 µL
+|200 μM
+|-
+|10 μM Forward Primer (D20)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (VR)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|1 ng
+|-
+|Q5 High-Fidelity DNA Polymerase
+|0.5 μl
+|0.02 U/μl
+|-
+|5X Q5 High GC Enhancer (optional)
+|5 µL
+|1X
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|40 cycles||98 °C||5 - 10 sec
+|-
+|58 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|16 °C
+|-
+|}
+'''Results:'''
+*negativ. Two 1% agarose gels were performed to prove the PCR product. Both were negativ.
+</div>
+<div class="general">
+=== Precipitation of eGFP ===
+'''Investigator:''' LK
+'''Aim of experiment:''' Determination of (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub> -concentration needed to precipitate eGFP.
+'''Procedure:'''
+* 50mL of eGFP solution (from fermentation) where gradually precipitated with rising concentrations (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub> (step size: 400mM)
+* All steps where performed at 4°C.
+* Pellets where solved in 10 mL 1x PBS.
+'''Results:'''
+''Extinction:''
+* Maximum Absorption at 488nm for eGFP. Absorption coefficient(eGFP,488): 53000 mol/Lcm.
+*
+{|cellspacing="1" border="1"
+|'''mM (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>'''
+|'''Dilution'''
+|'''Extinction'''
+|'''Concentration eGFP [µM]'''
+|-
+|400
+|1:10
+|0,197
+|37,0
+|-
+|800
+|1:10
+|0,084
+|15,8
+|-
+|1200
+|1:10
+|0,457
+|86,2
+|-
+|1600
+|1:100
+|0,16
+|301,8
+|-
+|2000
+|1:100
+|0,375
+|707,5
+|-
+|2400
+|1:10
+|0,505
+|95,3
+|-
+|2800
+|1:10
+|0,08
+|15,0
+|}
+[[File:Muc16_sds-page_160818.jpeg|250px]]
+</div>
+<div class="streptavidin">
+=== Inocculation of P258_E.coli_Bl-21 in M9 medium for fermentation ===
+'''Investigator: LK '''
+'''Procedure:'''
+* M9 medium with Cam (1:1000) was inocculated with preculture (~50 mL) of P258 (pASK111+Streptavidin)
+* the culture was incubated in the shaker over night at 37°C
+</div>
+<div class="hypoxia">
+=== Phosphorylation of F1005; F1016 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Phosphorylation of F1005; F1016
+'''Procedure:'''
+* 39 µL DNA
+* 5 µL 10x T4 PNK Bufer
+* 10 mM ATP
+* T4 PNK
+</div>
+<div class="hypoxia">
+=== Phosphorylation of O31; O32 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Phosphorylation of O31; O32
+'''Procedure:'''
+* 0.5 µL Oligonucleotides (10µM)
+* 2 µL 10x T4 PNK Bufer
+* 2 µL 10 mM ATP
+* 1 µL T4 PNK
+* 14.5 µL H2O
+* 95 °C; 3 min
+</div>
+<div class="hypoxia">
+=== Hybridization of phosphorylated O31; O32 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Hybridization of phosphorylated oligonucleotides: O31; O32
+'''Procedure:'''
+* 2 µL O31
+* 2 µL O32
+* 200 µL ddH20
+* 37 °C 20 min
+*75 °C 10 min
+</div>
+=='''Wednesday, August 17'''==
+<div class="hypoxia">
+=== Gelelectrophoresis of GSY7  ===
+'''Investigator: EF'''
+'''Aim of experiment: gelelectrophoresis of the remaining product of GSY7 PCR (from 16.8.16)'''
+'''Procedure:'''
+Agarose gelelectrophoresis was performed using an increased amount of SYBR Green
+'''Results'''
+There was no PCR product identified.
+</div>
+<div class="hypoxia">
+=== Plasmidpreparation of liquid culture of P64; P73 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of P64; P73
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|P64
+|pSB1C3
+|VEGF-p2a-PDGF
+|-
+|P73
+|pSB1C3
+|Poly-A
+|}
+'''Procedure:'''
+* According to Mini-prep. kit, SLG
+'''Results:''''
+* P64 134.4 ng/µL
+* P73 149.4 ng/µL
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of F1015 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="receptor">
+==='''PCR of scAvidin'''===
+'''Investigator: Julian'''
+'''Aim:''' Extraction of single chain Avidin from vector for further cloning
+'''Procedure:'''
+* reaction was performed after SOP (PCR Using Q5® High-Fidelity DNA Polymerase, NEB)
+* 2 ng Plasmid were used for amplification (1 µL)
+* Primers: O-27 and O-28
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial denaturation||98||120
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|64||30
+|-
+|72||300
+|-
+|final extension||72||300
+|-
+|Hold||4||ꝏ
+|}
+</div>
+<div class="receptor">
+=== Quickchange of P206 and P239 to correct BAP===
+'''Investigator: Julian'''
+'''Aim:''' Quickchange P206 (BAP-NanoLuc) and P239 (BAP-NanoLuc-A3C5) to correct BAP
+'''Procedure:'''
+* reaction was performed after SOP (PCR usingPfuUltra II Fusion HS DNA Polymerase, Agilent)
+* 10 ng Plasmid were used for amplification (2.5 µL)
+* Primers: O-33 and O-34
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial denaturation||98||120
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|55||30
+|-
+|68||300
+|-
+|final extension||68||360
+|-
+|Hold||4||ꝏ
+|}
+</div>
+<div class="streptavidin">
+=== Inocculation of fermenter ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* centrifuge preculture (P258 in M9 medium)
+* resuspend pellet in HCDF medium of fermenter and inocculate
+* pO<sub>2</sub>= 60 %; Temp= 37°C, pH~7
+* growth over night
+</div>
+=='''Thursday, Aug 18th'''==
+<div class="hypoxia">
+=== PCR of gene synthesises 8 with Q5 polymerase ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' Amplification of GSY7 with optimized Tm following negativ PCR reactions in order to amplify GSY7.
+'''Procedure:'''
+Approach:
+* 2,5 µl forward Primer VF2
+*2,5µl reverse Primer VR
+* 1µl dNTPs
+* 1µl DNA (1ng)
+* 10µl 5x Q5-Puffer
+* 0,5µl Q5-Polymerase
+* Fill up with water up to 50 µl
+Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)
+* 98°C_2min initiation step
+* 98°C_10sec
+* 62°C_30sec   >  step 2-4: 35 repeats
+* 72°C_1min
+* 72°C_5min final step
+* 4°_hold
+</div>
+<div class="hypoxia">
+=== PCR of gene synthesises 8 with Pfu Ultra II polymerase ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' Amplification of GSY7 with Pfu Ultra II polymerase following negativ PCR reactions in order to amplify GSY7.
+'''Procedure:'''
+Approach:
+* 2,5 µl forward Primer VF2
+*2,5µl reverse Primer VR
+* 1µl dNTPs
+* 1µl DNA (1ng)
+* 10µl Pfu Ultra II-Puffer
+* 0,5µl Q5-Polymerase
+* Fill up with water up to 50 µl
+Setup: (calculated with NEB calc. http://tmcalculator.neb.com/#!/)
+* 98°C_2min initiation step
+* 98°C_10sec
+* 56°C_30sec   >  step 2-4: 35 repeats
+* 72°C_2min
+* 72°C_5min final step
+* 4°_hold
+</div>
+<div class="streptavidin">
+=== Fermentation ===
+'''Investigator:''' NA
+'''Aim of the experiment:''' Streptavidin production
+'''Procedure:'''
+* exponential feed (Cam) for ~13 h (about 3-4 L); start at OD= 11.66
+* Induction of streptavidin expression (anhydro tetracyclin) at OD= 119
+* change of settings: pO2= 40 %; Temp= 30°C, pH~7
+* production over night
+</div>
+<div class="streptavidin">
+=== Streptavidin production in shaking flask===
+'''Investigator:''' NA
+'''Aim of the experiment:''' Streptavidin production
+'''Procedure:'''
+* 2 L LB medium (Cam 1:1000) was inocculated with ~10 ml M9 preculture (P258 in BL21)
+* induction with anhydro tetracycline (200µl, 2 mg/ml) at OD= 3,32
+* culture was incubated at 37 °C and 140 rpm for 4 hours
+* after expression, cultures were transferred into centrifuge tubes and spun down in the centrifuge (4 °C, 5000 rpm, 20 min, F4X1L rotor)
+* the supernatant was discarded, and the pellet was frozen away
+</div>
+<div class= "receptor">
+===Transformation of quickchanged P239 and 206 (BAP_Nanoluc_A3C5 and BAP_Nanoluc) ===
+'''Investigator: LK'''
+'''Procedure:'''
+* After DpnI-digestion 10µl of each plasmid was transformed into E.coli XL-1-blue.
+* Cells where plated out an Cam-plates after 1h of incubation without antibiotics.
+</div>
+<div class= "receptor">
+=== MiniPrep of F209 to P266 and P267, analytic digestion ===
+'''Investigator: JL'''
+'''Aim of the experiment:''' Verification of successful cloning.
+'''Procedure:'''
+MiniPrep was performed according to manufacturer's protocol (QIAprep MiniPrep, Qiagen)
+* Concentrations:
+<table cellspacing="0" border="1">
+<tr>
+<td><b>Plasmid</b>
+</td><td><b>c [ng/µl]</b>
+</td></tr>
+<tr>
+<td>P266
+</td><td>198
+</td></tr>
+<tr>
+<td>P267
+</td><td>200,8
+</td></tr></table>
+* Analytic digestion: 0.5 µl PstI, 0,5 µl EcoRI, 1 µl CutSmart, 6 µl ddH2O for P266 and P267 for 2 h at 37°C.
+* 1% agarose gel electrophoresis.
+'''Results:'''
+* Lane 1: 10 µl 1 kb Ladder.
+* Lane 2: Digest of F209 to P266.
+* Lane 3: Digest of F209 to P267.
+[[File:Muc16_miniPrep_of_P42_to_P50.png|500px]]
+</div>
+<div class="hypoxia">
+=== Phosphorylation of O31; O32 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Phosphorylation of O31; O32
+'''Procedure:'''
+* 5 µL Oligonucleotides (µM)
+* 2 µL 10x T4 PNK Bufer
+* 2 µL 10 mM ATP
+* 1 µL T4 PNK
+* 10 µL H2O
+* 95 °C 3min.
+</div>
+<div class="hypoxia">
+=== Hybridization of phosphorylated O31; O32 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Hybridization of phosphorylated oligonucleotides: O31; O32
+'''Procedure:'''
+* 2 µL O31
+* 2 µL O32
+* 200 µL ddH20
+</div>
+<div class="hypoxia">
+=== Plasmidpreparation of liquid culture of F1015 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of F1015
+{|cellspacing="0" border="1"
+|'''#'''
+|'''Plasmid'''
+|'''Description'''
+|-
+|F1015
+|pSB1C3
+|VEGF-p2a-PDGF + Poly-A
+|}
+'''Procedure:'''
+* According to Mini-prep. kit, SLG
+'''Results:''''
+* F1015 -> P1008 256.6 ng/µL
+</div>
+=='''Friday, Aug 19th'''==
+<div class="hypoxia">
+=== Gelelectrophoresis of GSY7  ===
+'''Investigator: EF'''
+'''Aim of experiment: gel electrophoresis of repeated GSY7 PCR (from 18.8.16)'''
+'''Procedure:'''
+Agarose gelelectrophoresis was performed at 90V
+'''Results'''
+There was no PCR product identified.
+</div>
+<div class="streptavidin">
+=== harvesting streptavidin ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* OD= 181
+* centrifuge culture for 1 h at 4800 rpm
+* freeze pellet (2033 g)
+</div>
+<div class="streptavidin">
+=== SDS PAGE Streptavidin fermentation ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' Verification of successfull production
+'''Procedure:'''
+* according to protocol
+* 8 µl Ladder; before induction; after induction; sample of shaking flask production after induction
+* all samples: 0.5/OD µl culture filled up with EB to 80µl + 20 µl SDS buffer; 10 µl on SDS gel
+'''Results:'''
+[[File:Muc16-deinemudder.jpg]]
+Clear bands of acetyl transferase (chloramphenicol resistance) in fermenter samples. Therefore cells kept plasmid. The streptavidin bands before and after induction do not differ. The fermentation was not succesful.
+The shaking flask sample however shows a brighter band for streptavidin.
+</div>
+<div class="general">
+=== Miniprep of F211 (pASK111(PAS Lys)), I739001 (Biobrick) and F206 (pASK111 vectorfragment) ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Miniprep of plasmids
+'''Procedure:'''
+* Miniprep was performed by manufacturers protocol (Qiaprep, Qiagen)
+* Plasmids were named:
+** F211 a: P268
+** F211 b: P269
+** I739001 a: P270
+** I739001 b: P271
+** F206 a: P272
+** F206 b: P273
+</div>
+<div class="general">
+=== Cloning of P260 in P261 and F215 in P74  ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Digestion, ligation and transformation
+'''Procedure:'''
+*
+</div>
+<div class="general">
+=== Transfection of HEK cells with P253, P225 and P226 ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Transfecting HEK cells with vectors encoding 3 diffrent types of signal peptides for secretion.
+'''Procedure:'''
+* HEK293 where cultured and seeded out on 12 cellculture dishes. (~5x10<sup>5</sup> cells per dish)
+* Transfection was performed on day 3 after seeding (60-70% confluency)
+* 10µg DNA of each signalpeptide mixed with 30µg PEI (polyenthylenimine) in ddH2O where incubated for 15 min and added to the cells, which where previously washed with PBS and covered (4mL) with optiMEM media. (Pen/Strep;No serum!)
+* After 4h of incubation at 37°C, 5% CO<sub>2</sub> the media was changed to RPMI (Pen/Strep; 5% FCS) again.
+</div>
+<div class="general">
+=== Picking of ''E.&nbsp;coli'' XL1 blue in quickchanged pSB1C3 in P239 and P206, Retrafo of P261 and P213 ===
+'''Investigator: JL'''
+'''Procedure:'''
+* Quickchanged pSB1C3 in P239: Colonies were picked from Cam-plates.
+* Retrafo of P261 and P213: Colonies were picked from Cam-plates.
+* Picked pipette tips was transferred into cell-culture tubes with air-permeable, sterile cover. Each tube contains 4&nbsp;mL of LB-medium + 4&nbsp;µL of the proper antibiotic.
+* These tubes were transferred in a cell culture shaker at 37&nbsp;°C and were incubated overnight
+</div>
+<div class="streptavidin">
+==='''Repeat of PCR of scAvidin'''===
+'''Investigator: Julian'''
+'''Aim:''' Extraction of single chain Avidin from vector for further cloning
+'''Procedure:'''
+* reaction was performed after SOP (PCR Using Q5® High-Fidelity 2X Master Mix, NEB)
+* 2 ng Plasmid were used for amplification
+* Primers: O-27 and O-28
+* annealing temperature was lowered to 60 °C
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial denaturation||98||120
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|60||30
+|-
+|72||150
+|-
+|final extension||72||300
+|-
+|Hold||4||ꝏ
+|}
+</div>
+<div class="general">
+==='''Repeat of PCR of Gene Synthesis 9'''===
+'''Investigator: Julian'''
+'''Aim:''' Amplification of gensynthesis 9 for further cloning
+'''Procedure:'''
+* reaction was performed after SOP (PCR Using Q5® High-Fidelity 2X Master Mix, NEB)
+* 2 ng Plasmid were used for amplification
+* Primers: VF2 and VR
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial denaturation||98||120
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|61||30
+|-
+|72||120
+|-
+|final extension||72||300
+|-
+|Hold||4||ꝏ
+|}
+</div>
+<div class="streptavidin">
+=== Preparative digestion of P8 (Streptavidin wt) ===
+'''Investigator: Julian'''
+'''Aim of experiment:'''  preparation for cloning of SA1 into pASK111
+'''Procedure:'''
+* preparative digestion batch
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|40&nbsp;µl
+|Plasmid DNA P8
+|-
+|5&nbsp;µl
+|Cutsmart (10x)
+|-
+|1.5&nbsp;µl
+|HindIII
+|-
+|1.5&nbsp;µl
+|XbaI
+|-
+|2&nbsp;µl
+|ddH2O
+|-
+|=50&nbsp;µl
+|'''TOTAL'''
+|}
+*duration: over night
+</div>
+=='''Saturday, Aug 20th'''==
+<div class= "receptor">
+=== Miniprep and analytical digestion of P274-P277 ===
+'''Investigator:''' LK
+'''Aim of the experiment:''' Isolating and verifiing A3C5+EspP_ddT ligation, "quickchanged" BAP-constructs and amplification of A3C5 in pSB1C3.
+'''Procedure:'''
+* Minipreps where performed according to manufacturer's protocol.
+* Analytical digestion with EcoRI and PstI of ~ 200-250ng of each plasmid was performed for 30 min at 37°C.
+'''Results:'''
+*
+</div>
+=='''Sunday, Aug 21st'''==
+<div class="general">
+=== Cloning of GSY9 and scAvidin ===
+'''Investigaor:''' LK, JL
+'''Procedure:'''
+* The PCR of scAvdin was digested over night with SpeI and NgoMIV at 37°C.
+* The PCR of GSY9 was divided: one half was digested with XbaI and AgeI (-> F224) and the other half was digested with XbaI and HindIII (->F225).
+* Additionally P74 (pSB1C3+RFP-Reporter) was digested with XbaI and AgeI (-> F227) to provide a plasmid for the ligation with F224.
+* The digestions where plotted on a gel, and bands at 1700Bp for scAvidin, 222Bp for TetO-OmpA, 490Bp for eMA and 2100Bp for pSB1C3 where cut out and purified with the Promega Wizard SV Gel Kit according to the manufactuerers protocol.
+* F224 (TetO-OmpA) was then ligated with F227 (pSB1C3), F225 (enhanced monomeric Avidin) was ligated with F206 (pASK111) and F226 (scAvidin) was ligated with F218 (pSB1C3). Ligations where incubated over night at 16°C.
+* Transformation was performed according to the SOP on Monday morning.
+</div>
+</div>
+=Week 15, Aug 22nd - Aug 28th=
+<div class="week" id="Week_15">
+=='''Monday, Aug 22nd'''==
+<div class="general">
+=== Sequencing of P268, P276, P277 and P279 ===
+'''Investigator: Julian'''
+'''Aim of the experiment:''' Sequencing of P268 (PAS lysine), P276 (QC BAP-NanoLuc-A3C5), P277 (QC BAP-NanoLuc) and P279 (A3C5-EspP-DoubleTerminator)
+'''Procedure:'''
+Sequencing batch were prepared after manufacturer's protocol. (15&nbsp;µl of plasmid DNA (50 - 100&nbsp;ng) and 2&nbsp;µl sequencing primer)
+* P268 (D20) FR12904429
+* P276 (VF2) FR12904428
+* P277 (VF2) FR12904427
+* P279 (VF2) FR12904426
+</div>
+<div class="receptor">
+=== Analytical digestion of P278 (pSB1C3(A3C5-EspP-doubleterminator) & P279 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' cofirm success of cloning
+'''Procedure:'''
+* Batch for analytical digestion for P278/P279 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2&nbsp;µl/ 1&nbsp;µl
+|Plasmid DNA P278/P279
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|1&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|5&nbsp;µl/ 6&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+'''Results:'''
+* P279 showed the expected signal at 1100 bp
+</div>
+<div class="receptor">
+=== Ligations of F1013 + gsy7; +gsy8 ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' cloning for further ligation steps
+'''Procedure:'''
+</div>
+<div class="hypoxia">
+</div>
+=='''Tuesday, Aug 23rd'''==
+<div class="general">
+=== Inoculation of Precultures of F228, F229 and F230 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Prepare cells for Miniprep
+'''Procedure:'''
+* Two colonies were picked from each plate
+* LB CAM was inoculated with F228 and F230
+* LB AMP was inoculated with F229
+* Precultures were incubated for 7 hours at 37°C
+'''Results:'''
+* Each preculture showed cell growth
+</div>
+<div class="general">
+=== Miniprep of F228, F229 and F30 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Obtain plasmids
+'''Procedure:'''
+* Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)
+* Plasmids were renamed:
+** F228 1: P281
+** F228 2: P282
+** F229 1: P283
+** F229 2: P284
+** F230 1: P285
+** F230 2: P286
+'''Results:'''
+* Concetrations in "Inventarliste"
+</div>
+<div class="hypoxia">
+=== Digestion of IRES-construct (F1019) by PmeI+NotI ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Prepare construct for ligation later on
+'''Procedure:'''
+µl DNA
+µl ddH2O
+µl of each enzyme
+µl cut smart buffer
+incubation at 37°C for 1 h
+Gel electrophoresis and gel extraction
+'''Results:'''
+Fragment was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.
+</div>
+</div>
+=='''Wednesday, Aug 24th'''==
+<div class="receptor">
+=== analytical digestion of P281, P282, P283, P284, P285 and P286 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Verify success of cloning
+'''Procedure:'''
+* Batch for analytical digestion of P281/P282 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|Plasmid DNA P281/P282
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|1&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|6&nbsp;µl/ 6&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P283/P284 with XbaI and HindIII-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|Plasmid DNA P283/P284
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|1&nbsp;µl
+|HindIII-HF
+|-
+|6&nbsp;µl/ 6&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P285/P286 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 1&nbsp;µl
+|Plasmid DNA P285/P286
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|1&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|6&nbsp;µl/ 6&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated at 37° for 1h
+'''Results:'''
+*
+</div>
+<div class="receptor">
+=== PCR of Genesynthesis 9 with VF2 and VR ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:''' Amplification of GSY9
+'''Procedure:'''
+* reaction was performed after SOP (Q5 Hotstart, NEB)
+* 2 ng Plasmid were used for amplification
+* Primers: VF2 and VR
+* Over all volume= 50&nbsp;µl
+*PCR program (standard):
+{|cellspacing="0" border="1"
+|'''Step'''
+|'''Temperature [°C]'''
+|'''Time [s]'''
+|-
+|initial denaturation||98||120
+|-
+|rowspan = "3"|35 cycles||98||10
+|-
+|66||30
+|-
+|72||30
+|-
+|final extension||72||300
+|-
+|Hold||4||ꝏ
+|}
+* PCR purification was performed according to manufacturers protocol (Wizard SV Gel and PCR clean-up kit, Promega)
+'''Results:'''
+*
+</div>
+<div class="hypoxia">
+=== PCR of linear pSB1C3   ===
+'''Investigator: MT'''
+'''Aim of the experiment:'''
+Amplification of linear pSB1C3 and introduction of restriction site: blunt at 5' and NotI at 3'
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (O-038)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (O-039)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|1 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||10 sec
+|-
+|68 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+</div>
+<div class="receptor">
+=== Preparative digestion of P74, P165, P196, P273, P274, P275, P285 and PCR of GSY9 ===
+'''Investigator: Clemens'''
+'''Aim of the experiment:'''
+'''Procedure:'''
+* Batch for preparative digestion of P74 with XbaI and AgeI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2&nbsp;µl
+|Plasmid DNA P74
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|23&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P74 with NgOMIV and AgeI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2&nbsp;µl
+|Plasmid DNA P74
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|23&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P165 with PstI-HF and AgeI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|12&nbsp;µl
+|Plasmid DNA P165
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|13&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P196 with NgOMIV and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA P196
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|10&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P273 with XbaI and HindIII-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|20&nbsp;µl
+|Plasmid DNA P273
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|1&nbsp;µl
+|HindIII-HF
+|-
+|5&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P274 with AgeI-HF and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl
+|Plasmid DNA P274
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|15&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P275 with NgOMIV and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|8&nbsp;µl
+|Plasmid DNA P275
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|17&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P285 with NgOMIV and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|12&nbsp;µl
+|Plasmid DNA P285
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|13&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of PCR of GS9 with NgOMIV, AgeI-HF and XbaI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|25&nbsp;µl
+|Plasmid DNA PCR GSY9
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|0&nbsp;µl
+|ddH2O
+|-
+|=31&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of PCR of GS9 with HindIII-HF and XbaI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|25&nbsp;µl
+|Plasmid DNA PCR GSY9
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|1&nbsp;µl
+|HindIII-HF
+|-
+|0&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated at 37° over night
+* Samples were applied on a 1% agarose gel
+* Samples were seperated for 45 min at 80V
+'''Results:'''
+* All Digests showed the expected lengths
+* Fragments were cut from the gel and purified according to manufacturers protocol (Wizard SV Gel and PCR clean-up system, Promega)
+</div>
+<div class="kill-switch">
+=== Transformation of P296 (pSB1C3 mGMK-Tk30, BBa_K782063) in xl1-blue ===
+'''Investigator: MT'''
+'''Aim of the experiment:''' Transformation for Poly-A-tail adding
+'''Procedure:'''
+transformation in competent xl1-blue according to protocol + rescue
+'''Result:'''
+plates (LB Cam) in incubator for further processing (37 °C) showed after 24 h colonies
+</div>
+<div class="hypoxia">
+=== (Re)ligations of F1013 (pSB1C3) and F1016 (phosphoryliert) + F1013 and F1005 in pSB1C3 ===
+'''Investigator: EF'''
+'''Aim of the experiment:''' Ligations of PCR Produkt from GSY8 in pSB1C3 vector for  later transformation and cloning
+'''Procedure:'''
+* Ligation mixtures were prepared as following; DNA amounts were calculated using the ligation calculator http://www.insilico.uni-duesseldorf.de/Lig_Input.html :
+* F1013+F1016: 1.6 μL F1013, 5 μL F1016, 2μL T4-DNA-Ligase-Buffer, 1 μL T4-DNA-Ligase, 10.4 μL ddH2O
+* F1013+F1005: 1.6 μL F1013, 2.2 μL F1005, 2μL T4-DNA-Ligase-Buffer, 1 μL T4-DNA-Ligase, 13.2 ddH2O
+* Ligation was incubated for 1.5 hours at 16 °C
+</div>
+<div class="Hypoxia">
+=='''Thursday, Aug 25th'''==
+</div>
+<div class="general">
+=== Phosphorylation and hybridization of O35, O36, O37 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+Phosphorylation and hybridization of O35, O36, O37
+'''Procedure:'''
+Phosphorylation
+* 0,5 µL Oligonucleotides
+* 2 µL 10x T4 PNK Bufer
+* 2 µL T4 Ligase Buffer
+* 1 µL T4 PNK
+* 14,5 µL H2O
+incubate at 37°C for 20 min and inactivate T4PNK (for 10 min at 75°C)
+Hybridization
+* 2 µL O31
+* 2 µL O32
+* in 200 µL ddH20
+incubate at 95°C for 3 min, let cool down slowly
+'''Results:'''
+</div>
+<div class="kill-switch">
+=== Inoculation of P296(Kill-Switch) ===
+'''Investigator: EU '''
+'''Aim of the experiment:''' production of P296
+'''Procedure:'''
+x5ml LB-CAM media, each inoculated by one colony (not by rescue colonies)
+'''Results:'''
+</div>
+<div class="hypoxia">
+=== Digestion of P74 + HincII ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P74 + HincII
+'''Procedure:'''
+* 3 µL DNA (1431 ng/µL)
+* 1 µL HincII
+* 14 µL ddH2O
+* 2 µL CutSmart buffer
+* incubation for 2h at 37 °C
+'''Results:''''
+[[File:Muc16_gelextraction_P74_HincII.png|250px]]
+* P74 -> P1021 111,2 ng/µL
+</div>
+<div class="receptor">
+=== Ligation of F233+F238, F236+F234, F233+F237, F232+F240, F231+F239, F235+F241 and F248+F249 ===
+'''Investigator: '''
+'''Aim of the experiment:'''
+* Ligation and transformation of XL1 blue
+'''Procedure:'''
+*Batch for Ligation of F233 and F238
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1,7&nbsp;µl
+|Vector F233
+|-
+|8,3&nbsp;µl
+|Insert F238
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F236 and F234
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1,1&nbsp;µl
+|Vector F236
+|-
+|8,9&nbsp;µl
+|Insert F234
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F233 and F237
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3,1&nbsp;µl
+|Vector F233
+|-
+|6,7&nbsp;µl
+|Insert F237
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F232 and F240
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|4,8&nbsp;µl
+|Vector F232
+|-
+|5,2&nbsp;µl
+|Insert F240
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F231 and F239
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|5,6&nbsp;µl
+|Vector F231
+|-
+|4,4&nbsp;µl
+|Insert F239
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F235 and F241
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6,5&nbsp;µl
+|Vector F235
+|-
+|3,5&nbsp;µl
+|Insert F241
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F228 and F249
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2,7&nbsp;µl
+|Vector F248
+|-
+|7,3&nbsp;µl
+|Insert F249
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* Ligations were performed according to SOP
+* XL1blue were transformed with the resulting fragments
+'''Results:''''
+Cellgrowth yes/no?
+</div>
+<div class="hypoxia">
+=== Digestion of P1007 + EcoRI + SpeI===
+'''Investigator: EF '''
+'''Aim of the experiment:'''
+* Digestion of P1007
+'''Procedure:'''
+* 10 µL DNA (3.6 ug)
+* 0.25 µL EcoRI
+* 0.25 µL SpeI
+* 34.5 µL ddH2O
+* 5 µL CutSmart Buffer NEB
+* incubation for 1h at 37 °C
+'''Results:'''
+</div>
+<div class="receptor">
+=== Preparative digestion, gel electrophoresis and gel extraction of P288 (CMV-Promotor) and P289 (NanoLuc + Streptag + Poly-A) ===
+'''Investigator: JL'''
+'''Aim of experiment: Preparative digestion, gel electrophoresis and gel extraction of P288 (CMV-Promotor) and P289 (NanoLuc + Streptag + Poly-A)'''
+'''Procedure:'''
+* Batches for analytical digestions:
+*P288: PstI and SpeI.
+*P29: PstI and XbaI.
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6 &nbsp;µl
+|Plasmid DNA
+|-
+|19 &nbsp;µl
+|ddH2O
+|-
+|3&nbsp;µl
+|CutSmart buffer (10x)
+|-
+|1&nbsp;µl
+|Each enzyme
+|-
+|30&nbsp;µl
+|'''TOTAL'''
+|}
+*Preparative gel electrophoresis was performed at 90&nbsp;V for 60&nbsp;min.
+*Preperative gel according to SOP.
+*The Purification was done according to the manufacturer's protocol.
+[[File:MUC16_gelextraction_P288_P289.jpeg]]
+</div>
+<div class="receptor">
+=== Analytical digestion and gelelectrophoresis of P293, P294, P295 (eMA pASK111) ===
+'''Investigator: JL'''
+'''Aim of the experiment:''' Analytical digestion and gelelectrophoresis of P293, P294, P295 (eMA pASK111).
+'''Procedure:'''
+* Batch for analytical digestion for P293, P294, P295.
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|2/1/4&nbsp;µl
+|Plasmid DNA P293/P294/P295
+|-
+|2&nbsp;µl
+|NEBuffer 4 (10x)
+|-
+|0.5&nbsp;µl
+|XbaI
+|-
+|0.5&nbsp;µl
+|HindIII (20&nbsp;U/µl)
+|-
+|6/8/4&nbsp;µl
+|ddH2O
+|-
+|=12&nbsp;µl
+|'''TOTAL'''
+|}
+* Incubation for 120&nbsp;min at 37&nbsp;°C.
+* Analytical gelelectrophoresis was performed at 90&nbsp;V for 30&nbsp;min.
+'''Results:'''
+{|cellspacing="0" border="1"
+|1&nbsp;kbp ladder DNA ladder
+|'''P293'''
+|'''P294'''
+|'''P294'''
+|-
+|}
+[[File:TUM13_20130423_RFP_Generator_RFC25_AgeI_NgoMIV.png|500px]]
+</div>
+=='''Friday, Aug 26'''==
+<div class="hypoxia">
+=== Digestion of P74 + HincII ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P74 + HincII
+'''Procedure:'''
+* 3 µL DNA (1431 ng/µL)
+* 1 µL HincII
+* 41 µL ddH2O
+* 5 µL CutSmart buffer
+* * 2h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_P74_HincII_2.png|250px]]
+generuler; pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2; P74[HincII]
+* F1024 49.3 ng\µL
+</div>
+<div class="hypoxia">
+=== Transformation of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Amplification of Vector
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="hypoxia">
+=== Digestion of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 + PmeI & NotI
+'''Procedure:'''
+* 7 µL DNA (77 ng/µL)
+* 0.25 µL PmeI
+* 0.25 µL NotI
+* 34.5 µL ddH2O
+* 5 µL CutSmart buffer
+* 2h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_P74_HincII_2.png|250px]]
+generuler; pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2; P74[HincII]
+* F1023 7.6 ng\µL
+</div>
+<div class="hypoxia">
+===  Gelextraction PCR pSB1C3 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Purification of PCR linear pSB1C3
+'''Procedure:'''
+* According to Gelextraction kit; Quiagen
+'''Results:'''
+[[File:Muc16_gelextraction_PCR_linear_pSB1C3.png|250px]]
+generuler; PCR gsy8; PCR linear pSB1C3
+* F1025 9.2 ng\µL
+</div>
+<div class="streptavidin">
+=== Analytical digestion of P249, P268 and P269 (each by XbaI&HindIII) ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Analyze construct for eventual preparative digestion
+'''Procedure:'''
+µl DNA (except for P249 --> 13 µl)
+µl ddH2O (except for P249 --> 4 µl)
+µl of each enzyme
+µl cut smart buffer
+incubation at 37°C for 2 h
+Gel electrophoresis and gel extraction
+'''Results:'''
+In each digestion only one fragment (the vector)  was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.
+</div>
+<div class="linkers">
+=== Preparative digestion of P272 and P273 (each by XbaI&HindIII) ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Prepare construct for ligation later on
+'''Procedure:'''
+µl DNA
+µl ddH2O
+µl of each enzyme
+µl cut smart buffer
+incubation at 37°C for 2 h
+Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according  to manufacturer’s protocol
+'''Results:'''
+Fragment was expected at about 4 kb. This could be shown comparing with 1kb DNA ladder.
+</div>
+<div class="kill-switch">
+=== Miniprep of P296 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Obtain plasmids
+'''Procedure:'''
+* Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)
+* Plasmid was not renamed.
+**
+'''Results:'''
+* Concetrations in "Inventarliste"
+</div>
+<div class="kill-switch">
+=== Sequencing of P296 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Sequencing of P296
+'''Procedure:'''
+*Sequencing batch was prepared after manufacturer's protocol:
+**7 µl of plasmid DNA (end concentration 50 - 100ng) in 8µl H2O
+**2 µl sequencing primer (one batch with VF2 and another with VR)
+*The different vectors we sequenced received the following barcodes:
+** P296 with VF2: FR
+** P296 with VR: FR
+'''Results:'''
+</div>
+<div class="hypoxia">
+=== Digestion of P1007, P1008 with EcoRI HF, SpeI HF + analytical gel ===
+'''Investigator: EF '''
+'''Aim of the experiment:''' Isolation of pSB1C3 plasmid from p1007)
+'''Procedure:'''
+* p1007 digested with:
+,25 µl EcoRI (HF)
+,25 µl SpeI (HF),
+µl CutSmart Buffer
+µg plasmid-DNA (P1007)
+fill up with ddH2O (Vtotal= 50µL)
+* 2x 25 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)
+'''Results:''' Despite optimised enzyme quantity the insert seems to not have been cut out of the plasmid. One single band at 3kb --> repeat reaction; check cutting sites with genious
+(*)has p1007 been sequenzed before(?). However the band was extracted from the geled and freezed labeled as "8.1"
+* p1008 digested with:
+,25 µl EcoRI (HF)
+,25 µl SpeI (HF),
+µl CutSmart Buffer
+µg plasmid-DNA (P1008)
+fill up with ddH2O (Vtotal= 50µL)
+* 2x 25 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)
+'''Results:''' Insert was isolated by gel extraction following GelExtraction Kit instructions.
+[[File:P1007, P1008_26.8.16_EF_black.scn|500px]]
+</div>
+=='''Saturday, Aug 27'''==
+<div class="hypoxia">
+=== PCR GSY8 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Amplification of GSY 8
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (VR)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (D20)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||10 sec
+|-
+|61 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+'''Results:'''
+* negativ two times :(
+</div>
+<div class="hypoxia">
+=== Mung Bean nuclease (MBN) digestion of F1023 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Get rid of overhangs. Preparation of DNA for blunt ligation
+'''Procedure:'''
+* 18 µL DNA (144 ng)
+* 2 µL MBN buffer
+* 0.5 µL MBN
+* 30 min; 30 °C
+* purification by PCR purification kit, Promega
+'''Results:'''
+* F1026 24 ng\µL; must be wrong, because this is more than digested. Endvolume 20 µL
+</div>
+<div class="hypoxia">
+=== Dephosphorylation of F1024 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Preparation of Vekor for blunt end Ligation
+'''Procedure:'''
+* 13 µL DNA (~50 ng\µL)
+* 5 µL Antarctic phosphatase (AP)
+* 2 µL AP buffer
+* 30 min ; 37 °C
+* heat inactivation: 2 min; 80 °C
+'''Results:'''
+* F1029
+</div>
+<div class="hypoxia">
+=== Ligation: F1025 +F1022 = F1027 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F1025 +F1022
+'''Procedure:'''
+* 1 µL F1025 (10 ng\µL)
+* 10 µL F1022 (5 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 6 µL ddH2O
+* 60 min;  30°C
+'''Results:'''
+* F1025 +F1022 = F1027
+</div>
+<div class="hypoxia">
+=== Ligation: F1025 +F1026 = F1028 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F1025 +F1026
+'''Procedure:'''
+* 1 µL F1025 (10 ng\µL)
+* 20 µL F1026 (24 ng\µL)
+* 3 µL buffer
+* 1 µL T4 ligase
+* 4 µL ddH2O
+* 60 min; 37 °C
+'''Results:'''
+* F1025 +F1026 = F1028
+</div>
+<div class="hypoxia">
+=== Phosphorylation of GSY7; GSY8 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Phosphorylation of GSY7; GSY8
+'''Procedure:'''
+* 5 µL DNA
+* 2 µL T4 Ligase buffer
+* 1 µL T4 PNK
+* 12 µL ddH20
+* 30 min; 37 °C
+* heat inactivation: 20 min; 65 °C
+'''Results:'''
+* F1030 (GSY7)
+* F1031 (GSY8)
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="hypoxia">
+=== Ligation: F1029 + F1030 = F1032; F1029 + F1031 = F1033  ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Ligation: F1029 + F1030 = F1032; F1029 + F1031 = F1033
+'''Procedure:'''
+* 5 µL F1029 ( ~ 30 ng) {ERROR!}
+* 10 µL F1030/F1031 (~ 25 ng)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 2 µL ddH2O
+* 60 min; 37 °C
+'''Results:'''
+* F1029 + F1030 = F1032
+* F1029 + F1031 = F1033
+*Both negativ, due to miscalculation
+</div>
+<div class="hypoxia">
+=== Transformation of F1027; F1028; F1032; F1033 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Amplification of Vector
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+=='''Sunday, Aug 28'''==
+<div class="hypoxia">
+=== PCR GSY8 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Amplification of GSY 8
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (D20)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (VR)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||10 sec
+|-
+|58 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+'''Results:'''
+*
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of F1032; F1028 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="hypoxia">
+=== Plasmidpreparation of liquid culture of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 ===
+'''Investigator: MP '''
+'''Aim of the experiment:'''
+Purification of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2
+'''Procedure:'''
+* According to Mini-prep. kit, SLG
+'''Results:''''
+* P1009 608.6 ng/µL
+</div>
+</div>
+=Week 16, Aug 29nd - Sep 4th=
+<div class="week" id="Week_16">
+=='''Monday, Aug 29nd'''==
+<div class="hypoxia">
+=== Plasmid preparation of liquid culture of F1032(clon 1); F1032(clon 2) ===
+'''Investigator: JL '''
+'''Aim of the experiment:'''
+Purification of F1032(clon 1); F1032(clon 2)
+'''Procedure:'''
+* According to Mini-prep. kit, Quiagen
+'''Results:'''
+* P 1010  448.4 ng/µL
+* P 1011 344.6 ng/µL
+</div>
+<div class="hypoxia">
+=== Analytical digestion of P1010; P1011 ===
+'''Investigator: JL '''
+'''Aim of the experiment:'''
+* verify constructs: P1010; P1011
+'''Procedure:'''
+* 2 µL DNA
+* 0.5 µL EcoRI
+* 0.5 µL PstI
+* 1 µL CutSmart buffer
+* 6 µL ddH20
+'''Results:'''
+[[File:Muc16_analytical_digest_P1010_P1011.png|250px]]
+* 1kb ladder; P1010; P1011
+</div>
+<div class="hypoxia">
+=== PCR and purification of GSY7_new and GSY8  ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Amplification of GSY 7_new and GSY 8
+'''Procedure:'''
+Same procedure for both GSYs:
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (VR)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (D20)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||10 sec
+|-
+|98 °C
+|30 sec
+|-
+|61 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+Purification according to Promega PCR purification kit
+'''Results:'''
+GSY7: 9,4 ng/µl
+GSY8: 1,5 ng/µl, probably contaminated with GSY7_new
+</div>
+<div class="hypoxia">
+=== Phosphorylation of GSY7_new and GSY8 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Phosphorylation of GSY7_new; GSY8
+'''Procedure:'''
+* 5 µL DNA
+* 2 µL T4 Ligase buffer
+* 1 µL T4 PNK
+* 12 µL ddH20
+* 30 min; 37 °C
+* heat inactivation: 10 min; 75 °C
+'''Results:'''
+* F1034 (GSY7_new)
+* F1035 (GSY8)
+</div>
+<div class="hypoxia">
+=== Ligation: F1034 + F1029 = F1036; F1035 + F1029 = F1037  ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Ligation: F1034 + F1029 = F1036; F1035 + F1029 = F1037
+'''Procedure:'''
+* 5 µL F1029 ( ~ 10 ng)
+* 10 µL F1034/F1035 (~ 25 ng)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 2 µL ddH2O
+* 60 min; 37 °C
+'''Results:'''
+* F1029 + F1034 = F1036
+* F1029 + F1035 = F1037
+</div>
+<div class="receptor">
+=== Preparative digestion of P297, P299, P279, P285, P285, P277, P312 & P251 ===
+'''Investigator:  ''' Clemens
+'''Aim of the experiment:'''
+Preparation for cloning in pSB1C3/pASK111
+'''Procedure:'''
+* * Batch for preparative digestion of P297 with AgeI-HF & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|5&nbsp;µl
+|Plasmid DNA P297
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|AgeI HF
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|220&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P299 with NgOMIV and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P299
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|19&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P279 with NgOMIV & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|20&nbsp;µl
+|Plasmid DNA P279
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|5&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* * Batch for preparative digestion of P285 with AgeI-HF & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA P297
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|AgeI HF
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|10&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* * Batch for preparative digestion of P277 with AgeI-HF & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P277
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|AgeI HF
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|19&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* * Batch for preparative digestion of P312 with AgeI-HF & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|5&nbsp;µl
+|Plasmid DNA P312
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|AgeI HF
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|20&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P251 with NgOMIV & PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA P251
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|10&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated for 3h at 37°C
+* Fragments were cut from the gel and purified by gelectraction (promega)
+'''Results:'''
+* Fragments were renamed (see Inventarliste) and concentrations were measured
+</div>
+<div class="receptor">
+=== Ligation of F254+ F255, F256+F257, F256+F258 & F260+F312 ===
+'''Investigator: ''' Clemens
+'''Aim of the experiment:'''
+* Ligation
+'''Procedure:'''
+*Batch for Ligation of F254 and F255
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|3&nbsp;µl
+|Vector F254
+|-
+|7&nbsp;µl
+|Insert F255
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F257 and F256
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.9&nbsp;µl
+|Vector F257
+|-
+|8.1&nbsp;µl
+|Insert F256
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F258 and F256
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.3&nbsp;µl
+|Vector F258
+|-
+|8.7&nbsp;µl
+|Insert F256
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+*Batch for Ligation of F312 and F260
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1.2&nbsp;µl
+|Vector F312
+|-
+|8.8&nbsp;µl
+|Insert F260
+|-
+|2&nbsp;µl
+|10X DNA-Ligase-buffer
+|-
+|1&nbsp;µl
+|T4-Ligase
+|-
+|7&nbsp;µl
+|H₂O
+|-
+|=20&nbsp;µl
+|'''TOTAL'''
+|}
+* Ligations were performed according to SOP
+</div>
+<div class="streptavidin">
+=== Analytical digestion and gelelectrophoresis of pASK111, P268 (SUMO-PAS), P6, and P259 (both SA) ===
+'''Investigator: Niklas'''
+'''Aim of the experiment: verification before cloning for fermentation'''
+'''Procedure:'''
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''P268/ P259/ P6/ pASK111'''
+|-
+|5,8 µl/ 17 µl/ 8,33 µl/ 14,2 µl
+|Plasmid DNA
+|-
+|2 µl
+|cut smart (10x)
+|-
+|0.5&nbsp;µl
+|XbaI
+|-
+|0.5&nbsp;µl
+|HindIII
+|-
+|11,2 µl/ 0 µl/ 8,67 µl/ 2,8 µl
+|ddH2O
+|-
+|=20 µl
+|'''TOTAL'''
+|}
+* Incubation for 90 min at 37&nbsp;°C.
+* Analytical gelelectrophoresis was performed at 90&nbsp;V for 60&nbsp;min.
+'''Results:'''
+[[File:Muc16_asdfghjklmnbv.jpg]]
+* on of the enzymes was contaminated
+</div>
+<div class="general">
+=== Transformation of P310 in BL 21; P6, P259, P268, pASK111, F1034+F1028 in xl1-blue ===
+'''Investigator: NA'''
+'''Procedure:'''
+* CaCl<sub>2</sub>-competent ''E.&nbsp;coli'' cells were taken from the stock in &ndash;80&nbsp;°C freezer and gently thawed on ice
+* 1&nbsp;µl (retrafo)/ 7 µl (ligation) of DNA was added to 50 µl of competent cells and gently mixed
+* 30&nbsp;min incubation on ice
+* 5&nbsp;min heat shock at 37&nbsp;°C
+* Added 0,9 ml LB medium to each tube
+* Incubation for 60&nbsp;min at 37&nbsp;°C in the 180&nbsp;rpm cell-culture shaker
+* 50&nbsp;µl of the cell suspension was plated on one plate
+* The rest were centrifuged for 1&nbsp;min at 13,000&nbsp;rpm and the supernatant was dicarded
+* The pellet was resuspended in 50&nbsp;µl of LB-medium and this concentrated cell suspension was plated on a  plate.
+</div>
+=='''Tuesday, Aug 30rd'''==
+<div class="general">
+=== PCR on GSY7 and GSY8 ===
+'''Investigator: CG '''
+'''Aim of the experiment:'''
+* Amplification of GSY 7 and GSY 8
+'''Procedure:'''
+Same procedure for both GSYs:
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (VR)
+|1,5 μl
+|0.25 μM
+|-
+|10 μM Reverse Primer (D20)
+|1,5 μl
+|0.25 μM
+|-
+|Template DNA
+|2 µL
+|10 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|45 cycles||98 °C||10 sec
+|-
+|98 °C
+|30 sec
+|-
+|60 °C
+|90 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+'''Results:'''
+* GSY8 negative: smear at the upper end of the gel.
+</div>
+<div class="receptor">
+=== Preparative digestion of P270 & P308 ===
+'''Investigator:  ''' Clemens
+'''Aim of the experiment:'''
+Preparation for cloning in pSB1C3
+'''Procedure:'''
+* Batch for preparative digestion of P270 with EcoRI-HF & Spe-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|25&nbsp;µl
+|Plasmid DNA P270
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF
+|-
+|1&nbsp;µl
+|SpeI-HF
+|-
+|0&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P308 with EcoRI-HF and XbaI
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|10&nbsp;µl
+|Plasmid DNA P308
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|15&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated for 3h at 37°C
+* Fragments were cut from the gel and purified by gelectraction (promega)
+'''Results:'''
+* Fragments were renamed (see Inventarliste) and concentrations were measured
+</div>
+<div class="general">
+=== Cloning of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) in pSB1C3 ===
+'''Investigator:  CG'''
+'''Aim of the experiment:'''
+Cloning of pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) in pSB1C3
+'''Procedure:'''
+* 17 µl pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) digestion with 1 µl Mung Bean Nuclease and 2 µl buffer for 30 min. at 30°C to receive blunt ends
+* Ligation of  8.7 µl pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 (PmeI+NotI) and 1.3 µl pSB1C3
+* Overnight incubation at 16 °C
+</div>
+<div class="general">
+=== Retransformation of P258  ===
+'''Investigator: CG '''
+'''Aim of the experiment:'''
+* Amplification of Vector
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="general">
+=== Digestion of P1005, P1006, P1007 with XbaI, PstI HF + analytical gel ===
+'''Investigator: EF '''
+'''Aim of the experiment:''' Isolation of insert for further construction of hypoxia system
+'''Procedure:'''
+* p1005, p1006, p1007 digested with:
+,25 µl EcoRI (HF)
+,25 µl SpeI (HF),
+µl CutSmart Buffer
+µg plasmid-DNA (Pp1005, p1006, p1007)
+fill up with ddH2O (Vtotal= 50µL)
+* 30 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)
+* Digestions were incubated for 1h at 37°C
+'''Results:''' Insert and vector were clearly separated. All cut vector remained at the expected position of 2kb. Inserts were isolated following extraction kit protocol . F number and concentrations were included into the Inventarliste. Remain of 30µl (with dye) frozen at -20 C -> Labeled as 5.1; 6,1; 7.2
+</div>
+<div class="hypoxia">
+=== Digestion of  P1007 with EcoRI HF, SpeI HF + analytical gel ===
+'''Investigator: EF '''
+'''Aim of the experiment:''' Isolation of vector. Verification of digestion performed on 29th, Friday
+'''Procedure:'''
+*p1007 digested with:
+,25 µl EcoRI (HF)
+,25 µl SpeI (HF),
+µl CutSmart Buffer
+µg plasmid-DNA (p1007)
+fill up with ddH2O (Vtotal= 50µL)
+* Digestion was incubated for 1h at 37°C
+* 30 µl on 1% agarose gel for electrophoresis (2log DNA-ladder as standard)
+'''Results:''' Again plasmid wasn´t cut. One single band at 3kb. Further procedur: sequence plasmid (?) repeat ligation to generate p1007. Isolate pSB1C3 from another plasmid.
+[File to be uploaded]
+</div>
+<div class="general">
+=== Ligation of F1001 and F1002 ===
+'''Investigator: EF '''
+'''Aim of the experiment:''' generate p1007 due to gel results (since 28th, Thursday)
+'''Procedure:'''  Ligation was performed as follows: 6,3 µl F1001, 5,3 µl F1002, 2 µl T4-DNA-Ligase Buffer, 1 µl T4-DNA-Ligase, filled up with ddH20 to 20 µl *3:1 vector-insert ratio
+</div>
+<div class="hypoxia">
+=== Ligation of F248 and 1015 ===
+'''Investigator: EF '''
+'''Aim of the experiment:'' hypoxia
+'''Procedure:''' Ligation was performed as follows: 1 µl F248, 5 µl F1015, 2 µl T4-DNA-Ligase Buffer, 1 µl T4-DNA-Ligase, filled up with ddH20 to 20 µl *Approximate 3:1 vector insert ratio
+'''Results''': Plates incubating over night at 37C
+</div>
+<div class="general">
+=== Sequencing of P259 (SA from GSY6; P303 and P304 (eMA)  ===
+'''Investigator: NA'''
+'''Procedure:'''
+* Sequencing batch were prepared after manufacturer's protocol. (15 µl of plasmid DNA (50 - 100 ng) and 2 µl sequencing primer) - all samples: VF2
+* barcodes in stock list
+</div>
+<div class="general">
+=== Picking of of ''E.&nbsp;coli'' XL1 blue with P6, pASK111, P268 ===
+'''Investigator: NA'''
+'''Procedure:'''
+* 2 colonies were picked.
+* These tubes were transferred in a cell culture shaker at 37&nbsp;°C and were incubated overnight
+</div>
+<div class="streptavidin">
+=== Inocculation of preculture (P310 eMA-HisTag) ===
+'''Investigator: NA'''
+'''Procedure:'''
+* 2 colonies were picked (20 mL LB with Cam)
+* the preculture was transferred in a cell culture shaker at 37&nbsp;°C and were incubated overnight
+</div>
+<div class="general">
+=== harvesting SUMO Protease===
+'''Investigator: NA'''
+'''Aim of the experiment:''' SUMO Protease production
+'''Procedure:'''
+* 6 x 2 L cultures
+* centrifuge cultures for 30 min at 6000 rpm
+* freeze pellet (120.5 g)
+</div>
+=='''Wednesday, Aug 31st'''==
+<div class="hypoxia">
+=== Over night liquid cultures of P1007 and P1012 ===
+'''Investigator: EF '''
+'''Aim of the experiment:'''
+Obtaining enough cellmass for plasmid preparation. Liquid cultures of Turbo and XL1 blue cells.
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+<div class="hypoxia">
+=== Phosphorylation of F1036 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Phosphorylation of F1036
+'''Procedure:'''
+* 36 µL DNA (*350 ng)
+* 4 µL T4 ligase buffer
+* 1 µL PNK
+* 30 min; 37 °C
+* heat deactivation: 20 min; 65 °C
+</div>
+<div class="hypoxia">
+=== Ligation: F1029 + F1037 = F1038 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Ligation: F1029 + F1037 = F1038
+'''Procedure:'''
+* 0.5 µL F1029 (30 ng\µL)
+* 10 µL F1037 (9 ng\µL)
+* 2 µL  T4 ligase buffer
+* 1 µL T4 ligase
+* 7 µL ddH2O
+* over night ; 16 °C
+'''Results:'''
+* F1029 + F1037 = F1038
+</div>
+<div class="general">
+=== Miniprep of various plasmids, analytical digestion, sequencing ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Obtain plasmids for: eMA, PAS-Lys-Sumo, pASK111, Streptavidin (non-codon-optimized)
+'''Procedure:'''
+* Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)
+* Digestion of about 250 ng for each eMA plasmid with EcoRI and PstI
+'''Results:'''
+* Names and concetrations in "Inventarliste"
+* Sequencing results
+* Gel:
+. GSY8, 2. - 5.: P319-P322 with EcoRI / PstI
+[[File:Muc16_160831_CG1.jpeg|500px]]
+</div>
+<div class="streptavidin">
+=== Cloning of Streptavidin (non-codon-optimized) into pASK111 ===
+'''Investigator: JL, NA, CG'''
+'''Aim of the experiment:''' Obtain Streptavidin (non-codon-optimized) in expression vector
+'''Procedure:'''
+* Preparative digestion of 42 µl P6 (Streptavidin) and 42 µl P315, 5 µl CutSmart and 1.5 µl XbaI/HindIII
+* Gel extraction
+* Ligation: 5.9 µl pASK111 + 4.1 µl SA + 2 µl ligase buffer + 7 µl ddH2o + 1 µl T4 ligase
+* Transformation according to SOP
+'''Results:'''
+* Gel:
+. Streptavidin (non-codon-optimized), 2. pASK111
+[[File:Muc16_160831_CG2.jpeg|500px]]
+</div>
+<div class="kill-switch">
+=== Preparative digestion of P296 and P73 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Prepare construct for ligation later on
+'''Procedure:'''
+µl DNA
+µl ddH2O
+µl of each enzyme (P296 --> EcoRI&SpeI, P73 --> EcoRI&XbaI)
+µl cut smart buffer
+incubation at 37°C for 3 h
+Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according  to manufacturer’s protocol
+'''Results:'''
+Fragments were expected at about 1 kb (P296) and 2,5 kb (P73). This could be shown comparing with 1kb DNA ladder.
+</div>
+<div class="kill-switch">
+=== Ligation: F269 + F270 = F271 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Ligation: F269 + F270 = F271
+'''Procedure:'''
+* 5 µL F269 ( ~  ng)
+* 10 µL F270 (~  ng)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 2 µL ddH2O
+* ONT; 16 °C
+'''Results:'''
+* F269 + F270 = F271
+</div>
+<div class="hypoxia">
+=== PCR and purification of GSY7_new and GSY8  ===
+'''Investigator: CG, EU '''
+'''Aim of the experiment:'''
+* Amplification of GSY 7_new and GSY 8
+'''Procedure:'''
+Same procedure for both GSYs:
+* PCR using PfuUltra II Fusion HotStart DNA Polymerase  according to manufacturer’s online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''10 µL reaction'''
+|'''Final concentration'''
+|-
+|PfuUltra II Hotstart PCR Master Mix
+|25 µL
+|1 X
+|-
+|10 μM Forward Primer (O-038)
+|2,5 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (O-039)
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|2 min
+|-
+|rowspan = "3"|40 cycles||98 °C||10 sec
+|-
+|98 °C
+|20 sec
+|-
+|45-64,7 °C (gradient)
+|20 sec
+|-
+|Final extension
+|72 °C
+|30 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+Purification according to Promega PCR purification kit
+'''Results:'''
+no amplification recognizable
+</div>
+<div class="general">
+=== harvesting SUMO Protease===
+'''Investigator: NA'''
+'''Aim of the experiment:''' SUMO Protease production
+'''Procedure:'''
+* resuspend pellet in PBS + 10 mM EDTA
+* homogenize cells with PANDA
+* centrifuge cultures for 30 min at 8000 rpm (protein in supernantant)
+* dialysis against IMAC buffer
+</div>
+<div class="general">
+=== Inocculation and induction of eMA-HisTag (P310) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* 2 L LB shaking flask
+* the cell culture was incubated at 37&nbsp;°C
+* induction with 200 µl anhydro tetracycliine (2mg/ml)  at OD= 0,55
+* production over night
+</div>
+=='''Thursday, Sep 1st'''==
+<div class="receptor">
+=== Miniprep of F261, F262, F263, F264, I739001, P305 & P258 ,analytical digestion and sequencing===
+'''Investigator: Clemens '''
+'''Aim of the experiment:'''
+Confirm sucessful cloning
+'''Procedure:'''
+* Miniprep was performed according to manufacturer's protocol (QIAprep, Qiagen)
+* Analytic digestion was performed to check if the cloning was successful
+* Batch for analytical digestion of P323/P324 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P323/P324
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P325/P326 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P326/P325
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P327/P328 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|1&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P328/P327
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P329/P330 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|0.5&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P329/P330
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7.5&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P331/P332 with PstI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|0.5&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P331/P332
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7.5&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for analytical digestion of P333/P334/P322 with AgeI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|0.5&nbsp;µl/ 0.5&nbsp;µl/ 0.5&nbsp;µl
+|Plasmid DNA P333/P334/P322
+|-
+|1&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|0.5&nbsp;µl
+|EcoRI-HF (10&nbsp;U/µl)
+|-
+|0.5&nbsp;µl
+|PstI-HF (20&nbsp;U/µl)
+|-
+|7.5&nbsp;µl/ 7.5&nbsp;µl/ 7.5&nbsp;µl
+|ddH2O
+|-
+|=10&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated for 1.5h at 37°C
+* Samples were run on an 1% agarose gel for 45 min at 90V
+'''Results:'''
+* Except for P329, P330 and P322 all fragments were of the expected size
+* Cloning of the inserts of P29 and P30 was started again.
+For confirmation of the Sequence the following plasmids were send for sequencing:
+* P323 (VF2 & VR)
+* P331 (VF2)
+* P333 (VF2)
+* P328 (VF2)
+* P326 (VF2)
+</div>
+<div class="receptor">
+=== Preparative digestion of P333, P308, P331 and P301 ===
+'''Investigator: Clemens '''
+'''Aim of the experiment:'''
+* Cloning of new constructs
+'''Procedure:'''
+* Batch for preparative digestion of P333 with NgOMIV and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P333
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|19&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P333 with AgeI-HF and PstI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P333
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|1&nbsp;µl
+|AgeI-HF
+|-
+|19&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P308 with XbaI and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|15&nbsp;µl
+|Plasmid DNA P308
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|XbaI
+|-
+|1&nbsp;µl
+|EcoRI-HF
+|-
+|10&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P333 with SpeI-HF and EcoRI-HF
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|8&nbsp;µl
+|Plasmid DNA P331
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|EcoRI-HF
+|-
+|1&nbsp;µl
+|SpeI-HF
+|-
+|17&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Batch for preparative digestion of P301 with PstI-HF and NgOMIV
+{|cellspacing="0" border="1"
+|'''volume'''
+|'''reagent'''
+|-
+|6&nbsp;µl
+|Plasmid DNA P301
+|-
+|3&nbsp;µl
+|Cutsmart buffer (10x)
+|-
+|1&nbsp;µl
+|PstI-HF
+|-
+|1&nbsp;µl
+|NgOMIV
+|-
+|19&nbsp;µl
+|ddH2O
+|-
+|=30&nbsp;µl
+|'''TOTAL'''
+|}
+* Digestions were incubated for 3h at 37°C
+* Samples were applied on a 1% agarose gel and run at 90V for 45min
+'''Results:'''
+* Digestions of P308, P331 and P301 showed the expected fragment sizes.
+* These fragments were cut from the gel and purified by gelextraction (Promega)
+* Samples were renamed and given Fragmentnumbers
+* The Digestions of P333 showed fragments of unexpected length. The Ligation of eMA in pSB1C3 (previous step) failed. This ligation has to be repeated.
+</div>
+<div class="hypoxia">
+=== PCR and purification of GSY7_new and GSY8  ===
+'''Investigator: MP, EU '''
+'''Aim of the experiment:'''
+* Amplification of GSY 7_new and GSY 8
+'''Procedure:'''
+*PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+* each GSY was amplified two times; once with Q5 GC-Enhancer and once without
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''25 µL reaction'''
+|'''Final concentration'''
+|-
+|5X Q5 Reaction Buffer
+|5 µL
+|1 X
+|-
+|10 mM dNTPs
+|0.5 µL
+|200 μM
+|-
+|10 μM Forward Primer (D20)
+|1.25 μl
+|0.5 μM
+|-
+|10 μM Reverse Primer (VR)
+|1.25 μl
+|0.5 μM
+|-
+|Template DNA
+|1 µL
+|10 ng
+|-
+|Q5 High-Fidelity DNA Polymerase
+|0.25 μl
+|0.02 U/μl
+|-
+|Nuclease-Free Water
+|to 25 μl (minus 5µl for GC-Enhancer respectively)
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||5 - 10 sec
+|-
+|61 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|16 °C
+|-
+|}
+Note: Use of the NEB T m Calculator is highly recommended.
+Purification according to Promega PCR purification kit
+'''Results:'''
+no amplification GSY8 recognizable, GSY7did work
+</div>
+<div class="kill-switch">
+=== Transformation of F271 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Transformation of F271 for further application
+'''Procedure:'''
+* 3 µL DNA were added to blr cells
+* incubation on ice for 20 min
+* heatshock in 42°C for 40s
+* incubation on ice for 4 min
+* 700µl LB-medium were added
+* incubation for 1h in 37°C shaker
+* centrifugation for 3 min
+'''Results:'''
+</div>
+<div class="hypoxia">
+=== Transformation of F1038 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Transformation of F1038 for further application
+'''Procedure:'''
+* 3 µL DNA were added to blr cells
+* incubation on ice for 20 min
+* heatshock in 42°C for 40s
+* incubation on ice for 4 min
+* 700µl LB-medium were added
+* incubation for 1h in 37°C shaker
+* centrifugation for 3 min
+'''Results:'''
+</div>
+<div class="general">
+=== harvesting of eMA-HisTag ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* centrifugate at 6000 rpm for 30 min (OD= 6.15)
+* 11,1 g pellet
+* SDS-PAGE after protocol
+* resuspend pellet in 20 mM Tris/HCl + 50 mM NaCl
+* homogenize cells with PANDA
+* centrifuge 30 min at 18000 rpm
+* denaturate inclusion bodies in 16 ml Gnd-Chl (pH 1.5) over night
+'''results:'''
+[[File:Muc16_eMAHisTag1.jpg]]
+marker, eMA before induction, eMA after induction, ULP after induction (SUMO protease)
+</div>
+=='''Friday, Sep 2nd'''==
+<div class="receptor">
+=== Ligation of F274+F275, F276+F260 and F279+F240 ===
+'''Investigator: ''' Clemens
+'''Aim of the experiment:'''
+* Cloning of new constructs
+'''Procedure:'''
+'''Results:'''
+</div>
+<div class="general">
+=== harvesting of eMA-HisTag ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* add 4 ml Gnd-Chl because pellet did not dissolve over night, continue shaking for few hours
+* centrifugate for 15 min at 15000 rpm (protein in supernatant)
+* refolding in 1.5 L cold PBS over night
+</div>
+<div class="general">
+=== purification of SUMO protease using ÄKTA purifier ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* centrifugation
+* destroying DNA using ultrasonic for 10 min
+* sterilfiltration
+* purification due to HisTag affinity of protein to nickel in column (buffer: 20 mM Tris/HCl + 500 mM NaCl
+* over night
+'''Procedure:'''
+* purification stopped because of pressure alarm, was restarted an showed no SUMO protease in the sample
+</div>
+<div class="general">
+=== Cloning of extended MCS into pDSG and pcDNA5 vector ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Extending the MCS of pDSG and pcDNA5 for cloning of BioBricks
+'''Procedure:'''
+* Digestion of 5 µl P291 (pDSG) and 15 µl P339 (pcDNA) with SphI and NruI-HF for pDSG and MluI-HF for pcDNA5
+* Gelextraction of both signals at about 4 kb
+* Oligo-hybridzation of O35/O36 and O36/O37 wo prior phosphorylation to obtain a total concentration of 17 ng/µl
+* Ligation of oligo-hybridzation and vector-fragements according to calculations in the Inventarliste and overnight incubation at 16°C
+'''Procedure:'''
+* expected signals after digestion: pDSG with 4 kb and 1.7 kb (lane 1), pcDNA with 4 kb and 1 kb (lane 2)
+[[File:Muc16_160902_digestion_prep_gel_CC.jpeg|300px]]
+</div>
+<div class="general">
+=== Miniprep of 2x pcDNA5 vector and 2x Streptavidin (nco) in pASK111 ===
+'''Investigator: CG'''
+'''Aim of the experiment:''' Obtain plasmids for pcDNA5 vector and 2x Streptavidin (nco) in pASK111
+'''Procedure:'''
+* Miniprep was performed according to manufacturers protocol (QiaPrep, QIAGEN)
+</div>
+=='''Saturday, Sep 3nd'''==
+<div class="hypoxia">
+=== Transformation of F285; F286 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+Amplification of F285; F286
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="hypoxia">
+=== Digestion of P1009 + PmeI&NotI ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P1009 + PmeI&NotI
+'''Procedure:'''
+* 33 µL DNA (~600 ng/µL)
+* 2 µL PmeI
+* 1 µL NotI
+* 9 µL ddH2O
+* 5 µL CutSmart buffer
+* incubation for 1h at 37 °C
+'''Results:'''
+* F1039  80 ng/µL
+</div>
+=='''Sunday, Sep 4th'''==
+<div class="hypoxia">
+=== Phosphorylation of F1040 (PCR product GSY7) ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Phosphorylation of F1040 (PCR product GSY7)
+'''Procedure:'''
+* 15 µL F1040 (20 ng/µL)
+* 5 µL T4 Ligase buffer
+* 1 µL T4 PNK
+* 29 µL ddH20
+* 30 min; 37 °C
+* heat inactivation: 20 min; 65 °C
+'''Results:'''
+* F1041 (PCR product GSY7)
+</div>
+<div class="hypoxia">
+=== Mung Bean nuclease (MBN) digestion of F1039 (pAAV-CWS_MmZip14_EMCV-IRES_mTagBFP2 [PmeI+NotI]) ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Get rid of overhangs. Preparation of DNA for blunt ligation
+'''Procedure:'''
+* 18 µL F1039 ( 80 ng/µL)
+* 2 µL  10x CutSmart buffer
+* 0.25 µL MBN (10 u/µL)
+* 60 min; 30 °C
+* purification by PCR purification kit, Promega
+'''Results:'''
+* F1042 30 ng\µL
+</div>
+<div class="hypoxia">
+=== Ligation: F1042 +F1025 = F1043 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F1042 +F1025
+'''Procedure:'''
+* 5.5 µL F1025 (9.2 ng\µL)
+* 8.2 µL F1042 (35 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 3.5 µL ddH2O
+* over night; 16 °C
+'''Results:'''
+* F1042 +F1025 = F1043
+</div>
+<div class="hypoxia">
+=== Ligation: F1041 +F1029 = F1044 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F1041 +F1029
+'''Procedure:'''
+* 1.6 µL F1029 (30 ng\µL)
+* 23 µL F1041 (6 ng\µL)
+* 3 µL buffer
+* 1 µL T4 ligase
+* 1.3 µL ddH2O
+* over night; 16 °C
+'''Results:'''
+* F1041 +F1029 = F1044
+</div>
+<div class="hypoxia">
+=== Cloning of SUMO-PAS in pASK75===
+'''Investigator: JL, EF '''
+'''Aim of the experiment:'''
+Ligation of F158 and "P310" (JL) (SUMO+PAS-Lysin in pASK75):
+*5,6 µL
+*2,4 µL
+*2 µL
+*1 µL T4-DNA-Ligase
+*fill up with ddH2O to 20 µL
+Transformation in NEB Turbo cells of 10 µL ligation
+</div>
+=Week 17, Sep 5th - Sep 11th=
+<div class="week" id="Week_17">
+=='''Monday, Sep 5th'''==
+<div class="general">
+=== harvesting of eMA-HisTag ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* centrifugate after refolding at 11500 rpm for 30 min
+'''results:'''
+[[File:Muc16_eMAHisTag2.jpg]]
+marker, eMA before induction, after induction, after denaturation and refolding
+</div>
+<div class="hypoxia">
+=== Inocculation of P341 (E.coli Bl-21; 50 ml LB) in M9 medium for fermentation ===
+'''Investigator: NA'''
+'''Procedure:'''
+* M9 medium with Cam (1:1000) was inocculated with preculture (~50 mL) of P258 (pASK111+Streptavidin)
+* the culture was incubated in the shaker over night at 37°C
+'''results:'''
+* a 50 ml culture with Ecoli Bl21 was induced
+[[File:Muc16_erstgro.jpg]]
+the SDS PAGE shows no streptavidin expression after induction
+* next fermentation in pSA (not pASK111)
+</div>
+=='''Tuesday, Sep 6th'''==
+<div class="hypoxia">
+=== Phosphorylation of F1005, F1016 ===
+'''Investigator: EF '''
+'''Aim of the experiment:'''  to be completed
+</div>
+<div class="hypoxia">
+=== Ligation of F1045, F1046 ===
+'''Investigator: EF '''
+'''Aim of the experiment:'''  to be completed
+Ligation of F1005, F10016 (GelEx GSY8) in F1013
+</div>
+=='''Wednesday, Sep 7th'''==
+<div class="general">
+=== harvesting of eMA-HisTag ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' eMA-HisTag production
+'''Procedure:'''
+* precipitation with ammonium sulfate gradient (10% to 90%)
+* the percentage was increased in 10% steps, after each addition of ammonium sulfate the solution was centrifugated at 8500 rpm for 20 min
+* SDS-PAGE: samples of the supernatants
+'''results:'''
+[[File:Muc16_eMAHisTag3.jpg]]
+The pellets of the precipitations with 50%, 60% and 70% were pooled and dialysed against IMAC buffer
+Next step: Äkta
+</div>
+<div class="receptor">
+=== MidiPrep of pSB1C3 with RFP generator (P4) ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' purification of CMV Nanoluc StrepTag PolyA (P312)
+'''Procedure:'''
+MidiPrep was performed according to manufacturer's protocol (QIAprep MidiPrep, Qiagen)
+'''Results:'''
+ng/µl in 80 µl
+</div>
+<div class="streptavidin">
+=== Inocculation of fermenter ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* inocculation with 50 ml preculture (P20 in LB medium)
+* pO<sub>2</sub>= 60 %; Temp= 37°C, pH~7
+* growth over night
+* OD next morning: 0.4
+</div>
+=='''Thursday, Sep 8th'''==
+<div class="streptavidin">
+=== Fermentation ===
+'''Investigator:''' NA
+'''Aim of the experiment:''' Streptavidin production
+'''Procedure:'''
+* exponential feed (Amp) for ~13 h (about 3-4 L); start at OD= 7.5 (glucose test negative)
+* Induction of streptavidin expression (IPTG) at OD= 30
+* production over night
+</div>
+=='''Friday, Sep 9th'''==
+<div class="streptavidin">
+=== harvesting streptavidin ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* OD= 41.4
+* centrifuge culture for 1 h at 4800 rpm
+* resuspend pellet (275 g)in 20mM Tris HCl + 500 mM NaCl(pH 8)
+* homogenize with PANDA
+* the resulting lysate was transferred into centrifuge tubes and spun down (4°C, 9000 rpm, 30 mins). The supernatant was cast away and the pellet was resuspended in 6M Gua-HCl (pH = 1.5) at 4°C overnight.
+</div>
+=='''Saturday, Sep 10th'''==
+=='''Sunday, Sep 11th'''==
+<div class="streptavidin">
+=== harvesting streptavidin ===
+'''Investigator: NA'''
+'''Aim of the experiment:''' streptavidin production
+'''Procedure:'''
+* the denaturated protein solution was refolded in 15 L 1x PBS (added drop wise) over night
+* the solution was centrifugated at 9500 rpm for 20 minutes, the pellet was stored in the freezer, the supernatant will be concentrated via cross flow and precipitated with ammonium sulfate afterwards
+'''results:'''
+[[File:Muc16_strepfermreinigung.jpg]]
+</div>
+=Week 18, Sep 12th - Sep 18th=
+<div class="week" id="Week_18">
+=='''Tuesday, Sep 13th'''==
+<div class="hypoxia">
+=== Digestion of P74 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P74
+'''Procedure:'''
+F1055:
+* 2 µL DNA (1431 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL HincII (10 u/µL)
+* 16 µL ddH2O
+* incubation for 1h at 37 °C
+F1056:
+* 2 µL DNA (1431 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL HincII (10 u/µL)
+* 0.25 µL AgeI (20 u/µL)
+* 15.5 µL ddH2O
+* incubation for 1h at 37 °C
+F1057:
+* 2 µL DNA (1431 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL HincII (10 u/µL)
+* 0.25 µL NgoMIV
+* 15.5 µL ddH2O
+* incubation for 1h at 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_P74_div.png|250px]]
+Kb ruler, F1055[HincII], F105[HincII&AgeI]6, F1057[HincII&NgoMIV], P1017[EcoRI&SpeI]
+* F1055 49.5 ng/µL
+* F1056 37.0 ng/µL
+* F1057 29.7 ng/µL
+</div>
+<div class="hypoxia">
+=== Analytical digestion of P1017 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Analytical digestion of P1017
+'''Procedure:'''
+* 2 µL DNA (312 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL EcoRI
+* 15.5 µL ddH2O
+* incubation for 1h at 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_P74_div.png|250px]]
+Kb ruler, F1055[HincII], F105[HincII&AgeI]6, F1057[HincII&NgoMIV], P1017[EcoRI&SpeI]
+</div>
+<div class="hypoxia">
+=== PCR of GSY10   ===
+'''Investigator: MT'''
+'''Aim of the experiment:'''
+Amplification of GSY10
+'''Procedure:'''
+* PCR Using Q5® High-Fidelity DNA Polymerase (M0491) according to online protocol
+{|cellspacing="0" border="1"
+|'''Component'''
+|'''50 µL reaction'''
+|'''Final concentration'''
+|-
+|Q5® High-Fidelity 2X Master Mix
+|25 µL
+|1 X
+|-
+|10 μM VR
+|2,5 μl
+|0.5 μM
+|-
+|10 μM VF2
+|2,5 μl
+|0.5 μM
+|-
+|Template DNA
+|0.1 µL
+|1 ng
+|-
+|Nuclease-Free Water
+|to 50 μl
+|
+|}
+Thermocycling Conditions for a Routine PCR:
+{|cellspacing="0" border="1"
+|'''STEP'''
+|'''TEMP'''
+|'''TIME'''
+|-
+|Initial Denaturation
+|98 °C
+|30 sec
+|-
+|rowspan = "3"|35 cycles||98 °C||10 sec
+|-
+|62 °C
+|30 sec
+|-
+|72 °C
+|60 sec
+|-
+|Final extension
+|72 °C
+|120 sec
+|-
+|Hold
+|4 °C
+|-
+|}
+</div>
+<div class="hypoxia">
+=== Dephosphorylation of F1055 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Preparation of Vekor for blunt end Ligation
+'''Procedure:'''
+* 15 µL F1055 (~50 ng\µL)
+* 1 µL FastAP (1 u/µL)
+* 2 µL  10x FastAP buffer
+* 10 min ; 37 °C
+* heat inactivation: 5 min; 75 °C
+'''Results:'''
+* F348
+</div>
+<div class="hypoxia">
+=== Digestion of P1017 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P1017
+'''Procedure:'''
+* 10 µL DNA (312 ng/µL)
+* 5 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 34.5 µL ddH2O
+* incubation for 1h at 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p1017.png|250px]]
+Kb ruler, P1017[SpeI&PstI], P1017[SpeI&PstI], F362: PCR-GSY7[AgeI], PCR-GSY7, PCR-GSY8
+* F350
+</div>
+<div class="hypoxia">
+=== Over night liquid culture of P1009 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Getting enough cellmass for plasmid preparation
+'''Procedure:'''
+* Inoculation of 5 mL LB-medium (containing antibiotica) with colonies of foregone transformation
+* Incubate over night at 37 °C in shaker
+</div>
+=='''Wednesday, Sep 14th'''==
+<div class="hypoxia">
+=== Gelextraction of F357[NgoMIV]; P1006[XbaI&PstI] ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Gelextaction of F357[NgoMIV]; P1006[XbaI&PstI]
+'''Procedure:'''
+* Using gelextraction kit, Promega
+'''Results:'''
+[[File:Muc16_gelex_F364_F365.png|250px]]
+kb ladder, F357[NgoMIV]; P1006[XbaI&PstI]
+* F357[NgoMIV] -> F364 41 ng/µL
+* P1006[XbaI&PstI] -> F365 9.1 ng/µL
+</div>
+<div class="hypoxia">
+=== Ligation: F1057 + F364 = F366 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F1057 + F364
+'''Procedure:'''
+* 1,6 µL F1057 (29.7 ng\µL)
+* 2.1 µL F364 (41 ng\µL)
+* 3 µL buffer
+* 1 µL T4 ligase
+* 22.3 µL ddH2O
+* 30 min; RT
+'''Results:'''
+* F1057 + F364 = F366
+</div>
+<div class="hypoxia">
+=== Ligation: F350 + F365 = F367 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F350 + F365
+'''Procedure:'''
+* 2,6 µL F350 (19 ng\µL)
+* 2.1 µL F365 (9.1 ng\µL)
+* 3 µL buffer
+* 1 µL T4 ligase
+* 15.4 µL ddH2O
+* 30 min;  RT
+'''Results:'''
+* F350 + F365 = F367
+</div>
+<div class="hypoxia">
+=== Digestion of P1008 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P1008
+'''Procedure:'''
+* 10 µL P1008 (256.5 ng/µL)
+* 5 µL CutSmart buffer
+* 0.25 µL XbaI
+* 0.25 µL PstI
+* 34.5 µL ddH2O
+* incubation for 1h at 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p1008_2.png|250px]]
+Kb ruler, ... P1008[XbaI&PstI]
+* P1008 -> F368 ~1 ng/µL
+* Maybe do it again, fragments do not have the right size, apparently.
+</div>
+<div class="hypoxia">
+=== Transformation of F366; F367 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Amplification of Vector
+'''Procedure:'''
+* Transformation following SOP(13.02.2013)
+</div>
+<div class="kill-switch">
+=== Analytical digestion of P296 and F269 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Analyze construct for eventual preparative digestion
+'''Procedure:'''
+µl DNA
+µl ddH2O
+µl of PstI
+µl cut smart buffer
+incubation at 37°C over night
+Gel electrophoresis and gel extraction
+'''Results:'''
+</div>
+<div class="kill-switch">
+=== Preparative digestion of P313, P296 and P73 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Prepare construct for ligation later on
+'''Procedure:'''
+µl (P73)/ 15 µl (P296)/ 20 µl (P313) DNA
+µl of each enzyme (P296&P313 --> EcoRI&SpeI, P73 --> EcoRI&XbaI)
+µl cut smart buffer
+ad 50 µl ddH2O
+incubation at 37°C over night
+Gel electrophoresis and gel extraction by Gel extraction kit (Promega) according  to manufacturer’s protocol
+'''Results:'''
+* P296 [EcoRI&SpeI] --> F378
+* P313 [EcoRI&SpeI] --> F383
+* P73   [EcoRI&XbaI] --> F379
+</div>
+<div class="kill-switch">
+=== Ligation: F269 + F270 = F380; F269 + F92 = F381; F269 + F133 = F382  ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Ligation:
+** F269 + F270 = F380
+** F269 + F92 = F381
+** F269 + F133 = F382
+'''Procedure:'''
+* 3 µL F269 (6,3 ng)
+* 0,5 µL F270 (5,6ng)/ 0,25 µl F92 (6,75 ng)/ 0,25 µl F133 (13 ng)
+* 0,5 µL buffer
+* 0,5 µL T4 ligase
+* 0,5/0,75 µL ddH2O
+* ONT; 16 °C
+'''Results:'''
+* F269 + F270 = F380
+* F269 + F92 = F381
+* F269 + F133 = F382
+</div>
+<div class="kill-switch">
+=== Sequencing of P313 ===
+'''Investigator: EU'''
+'''Aim of the experiment:''' Sequencing of P313
+'''Procedure:'''
+*Sequencing batch was prepared after manufacturer's protocol:
+**6 µl of plasmid DNA (end concentration 58,6 ng) in 9µl H2O
+**2 µl sequencing primer (VF2)
+*The different vectors we sequenced received the following barcodes:
+** P313 with VF2: FR12904387
+'''Results:'''
+</div>
+=='''Thursday, Sep 15th'''==
+<div class="hypoxia">
+=== Digestion of P1008 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P1008
+'''Procedure:'''
+* 10 µL P1008 (256.5 ng/µL)
+* 5 µL CutSmart buffer
+* 0.25 µL XbaI
+* 0.25 µL PstI
+* 34.5 µL ddH2O
+* incubation for over night at 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p1008_3.png|250px]]
+P1008[XbaI&PstI], P1008[XbaI&PstI], 1Kb ruler
+* P1008[XbaI&PstI] -> F375  32 ng/µL
+</div>
+<div class="hypoxia">
+=== Ligation: F63 + F375 = F377 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F63 + F375
+'''Procedure:'''
+* 2.2 µL F63 (45 ng\µL)
+* 6.3 µL F375 (32 ng\µL)
+* 3 µL buffer
+* 1 µL T4 ligase
+* 17.5 µL ddH2O
+* 30 min; RT
+'''Results:'''
+* F63 + F375 = F377
+</div>
+<div class="hypoxia">
+=== Fill in of overhangs of F386 with Large Klenow fragment ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* 3' overhang removal and fill-in of 3' recessed (5' overhang) ends using DNA Polymerase I, Large (Klenow) Fragment
+* short: create blunt ends, needed for ligation
+'''Procedure:'''
+* 17.09 µL F386 (25.9 µL)
+* 0.66 µL 10 mM dNTP Mix
+* 2 µL T4 Ligase buffer
+* 0.25 µL Klenow Fragment
+* 15 min; RT
+* heat inactivation: 20 min; 75 °C
+'''Results:'''
+* F387
+</div>
+<div class="hypoxia">
+=== Incubation of F386 with Q5 polymerase ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Create blunt ends, needed for ligation
+'''Procedure:'''
+* 5 µL 2x Q5 Mastermix
+* 5 µL F386 (25.9 ng/µL)
+* 15 min; 72 °C
+'''Results:'''
+* F388
+</div>
+<div class="hypoxia">
+=== Ligation: F374 + F386 = F390 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F374 + F386
+'''Procedure:'''
+* 1 µL F374 (25.9 ng\µL)
+* 17.5 µL F387 (~ 22 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 30 min; RT
+'''Results:'''
+* F374 + F386 = F390
+</div>
+<div class="hypoxia">
+=== Ligation: F374 + F388 = F391 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F374 + F388 = F391
+'''Procedure:'''
+* 0.3 µL F374 (25.9 ng\µL)
+* 10 µL F388 (~ 13 ng\µL)
+* 2 µL T4 ligase buffer
+* 1 µL T4 ligase
+* 6.7 µL ddH2O
+* 30 min; RT
+'''Results:'''
+* F374 + F388 = F391
+</div>
+<div class="hypoxia">
+=== Transformation of F390, F391, F376 and F377 (INSULIN) ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Transformation of F390, F391, F376 and F377 for further application
+'''Procedure:'''
+* 3 µL DNA were added to xl1-cells
+* incubation on ice for 20 min
+* heatshock in 42°C for 40s
+* incubation on ice for 4 min
+* 700µl LB-medium were added
+* incubation for 1h in 37°C shaker
+* centrifugation for 3 min
+'''Results:'''
+</div>
+<div class="hypoxia">
+=== Transformation of F389 (zk-vector) ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Transformation of F389 for further application
+'''Procedure:'''
+* 3 µL DNA were added to xl1-cells
+* incubation on ice for 20 min
+* heatshock in 42°C for 40s
+* incubation on ice for 4 min
+* 700µl LB-medium were added
+* incubation for 1h in 37°C shaker
+* centrifugation for 3 min
+'''Results:'''
+</div>
+<div class="hypoxia">
+=== Transformation of F366 ===
+'''Investigator: EU '''
+'''Aim of the experiment:'''
+* Transformation of F366 for further application
+'''Procedure:'''
+* 3 µL DNA were added to xl1-cells
+* incubation on ice for 20 min
+* heatshock in 42°C for 40s
+* incubation on ice for 4 min
+* 700µl LB-medium were added
+* incubation for 1h in 37°C shaker
+* centrifugation for 3 min
+'''Results:'''
+</div>
+=='''Friday, Sep 16th'''==
+<div class="hypoxia">
+=== Digestion of P430 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P430
+'''Procedure:'''
+* 10 µL 430 (~150 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL PacI
+* 0.25 µL AgeI
+* 7.5 µL ddH2O
+* 1h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p430_etc.png|250px]]
+kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]
+* P430[PacI&AgeI] -> F400 2.1 ng/µL
+</div>
+<div class="hypoxia">
+=== Digestion of P424 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P424
+'''Procedure:'''
+* 17 µL 424 (60.9 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 1h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p430_etc.png|250px]]
+kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]
+* P424[SpeI&PstI] -> F401 15.7ng/µL
+</div>
+<div class="hypoxia">
+=== Digestion of P425 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of P425
+'''Procedure:'''
+* 10 µL 425 (~222 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 7.5 µL ddH2O
+* 1h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_p430_etc.png|250px]]
+kb ruler; P430[PacI&AgeI], P424[SpeI&PstI], P425[SpeI&PstI]
+* P425[SpeI&PstI] -> F402 53 ng/µL
+</div>
+</div>
+=Week 19, Sep 19th - Sep 25th=
+<div class="week" id="Week_19">
+=='''Tuesday, Sep 20th'''==
+<div class="hypoxia">
+=== Digestion of P444; P445; P446 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+* Digestion of  P444; P445; P446
+'''Procedure:'''
+P444:
+* 8 µL P444 (377.7 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 9.5 µL ddH2O
+* 1h; 37 °C
+P445:
+* 14 µL P445 (223.7 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 3.5 µL ddH2O
+* 1h; 37 °C
+P446:
+* 17.5 µL P446 (144 ng/µL)
+* 2 µL CutSmart buffer
+* 0.25 µL SpeI
+* 0.25 µL PstI
+* 1h; 37 °C
+'''Results:'''
+[[File:Muc16_gelextraction_P451_p4444_P446_etc.png|250px]]
+kb ruler P451[PacI&MluI], P451[PacI&MluI], P444[SpeI&PstI], P446[SpeI&PstI]
+-> I did P444 again, because there was marker in the line.
+[[File:Muc16_gelextraction_P451_p4444_P445_etc.png|250px]]
+kb ruler, P444[SpeI&PstI], P445[SpeI&PstI]
+* P444[SpeI&PstI]  -> F420  18 ng/µL
+* P445[SpeI&PstI]  -> F418  24.2 ng/µL
+* P446[SpeI&PstI]  -> F421  7.4 ng/µL
+</div>
+=='''Wednesday, Sep 21th'''==
+<div class="hypoxia">
+=== Ligation {F438 + F435} + F433 or F334 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation {F438 + F435} + F433 or F334
+'''Procedure:'''
+F438 + F435:
+* 10 µL F438 (40.2 ng/µL)
+* 11 µL F435 (30.5)
+* 2 µL T4 Ligase buffer
+* 1 µL T4 Ligase
+* 6 µL ddH2O
+{F438 + F435} + F433:
+* 0.5 µL F433 (48.2 ng/µL)
+* 4.5 µL {F438 + F435} (~24.4 ng/µL)
+* 2 µL T4 Ligase buffer
+* 1 µL T4 Ligase
+* 12 µL ddH2O
+{F438 + F435} + F434:
+* 0.5 µL F434 (109 ng/µL)
+* 4.5 µL {F438 + F435} (~24.4 ng/µL)
+* 2 µL T4 Ligase buffer
+* 1 µL T4 Ligase
+* 11.5 µL ddH2O
+'''Results:'''
+* F438 + F435 = F439
+* {F438 + F435} + F434 =  F440
+* {F438 + F435} + F433 = F441
+</div>
+=='''Sunday, Sep 25th'''==
+<div class="hypoxia">
+=== Ligation: F457 + F463 = F464 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F457 + F463
+'''Procedure:'''
+* 2.7 µL F457 (29.3 ng\µL)
+* 4.3 µL F463 (22.1 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 30 min;  RT
+'''Results:'''
+* F457 + F463 = F464
+</div>
+<div class="hypoxia">
+=== Ligation: F458 + F463 = F465 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F458 + F463
+'''Procedure:'''
+* 3.8 µL F458 (15.5 ng\µL)
+* 3.2 µL F463 (22.1 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* 30 min;  RT
+'''Results:'''
+* F458 + F463 = F465
+</div>
+<div class="hypoxia">
+=== Ligation: F434 + F464 = F466 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F434 + F464
+'''Procedure:'''
+* 0.5 µL F434 (109.1 ng\µL)
+* 6.5 µL F464 (17.4 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* over night; 16 °C
+'''Results:'''
+* F434 + F464 = F466
+</div>
+<div class="hypoxia">
+=== Ligation: F434 + F465 = F467 ===
+'''Investigator: MT '''
+'''Aim of the experiment:'''
+*Ligation: F434 + F465
+'''Procedure:'''
+* 0.4 µL F434 (109.1 ng\µL)
+* 6.6 µL F465 (12.96 ng\µL)
+* 2 µL buffer
+* 1 µL T4 ligase
+* over night; 16 °C
+'''Results:'''
+* F434 + F465 = F467
+</div>
+</div>
+=Week 20, Sep 26th - Aug 2th=
+<div class="week" id="Week_20">
+</div>

Difference between revisions of "Team:LMU-TUM Munich/Labjournal"

Latest revision as of 03:14, 20 October 2016

Labjournal

Samples

Transformation of E. coli XL1 blue with Phytochrome B (2–908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Miniprep of pTUM100 with pGAL, pTEF1, pTEF2, pADH and RFC25 compatible RFP generator

Sequencing of RFP-Generator (RFC25, pSB1C3)

Picking of of E. coli XL1 blue with Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Analytical digestion and gelelectrophoresis of RFP-generator (RFC25, pSB1C3, P4 & P5)

Sequencing of pTUM vectors with pGAL, pADH, pTEF1, pTEF2

Miniprep of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3)

Analytical digestion and gelelectrophoresis of Phytochrome B (2-908 N-terminal amino acids) (BBa_K801031, RFC25, pSB1C3), P7 - P10

Transformation of E. coli XL1 blue with

Week 1, May 16th - May 22nd

Monday, May 16th

Streptavidin Plasmid Check

Streptavidin Expression: Transform BL21

Tuesday, May 17th

SDS Gel Analysis

MiniPreps pSb1C3–AviTag, –A3C5 and pASK75–(SA1), –(SAm1)

Inoculation of Pre-Culture with BL21 (pASK75 (SA1)) in LB Medium

Wednesday, May 18th

Repeat Analytical Gel of pSb1C3–AviTag, –A3C5

Inoculation of BL21 (pASK75 (SA1)) Culture in 2 L TB Medium and Induction of Streptavidin Production by Addition of Tetracycline

Expression and Harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB Medium

Dialysis of eGFP

MiniPrep of quickchanged pNGAL146-A2 EspP

Sequencing of P14 (Avi-Tag), P15 (A3C5) & P19 (Quick change (QC) EspP in pNGAL-A2)

Digestion of P16 , P17, P18 & P19 (all QC EspP in pNGAL-A2) with AgeI & HindIII + analytical gel

Thursday, May 19th

Re-Sequencing of P19

Cloning of A3C5 and Avi-Tag into pSB1C3

Streptavidin refolding

Biotinylation of BSA

Friday, May 20th

Qualitative analysis of streptavidin expression

Cloning of A3C5 and Avi-Tag into pSB1C3

Transformation of Biobricks in XL1-blue

Ammonium sulfate precipitation of streptavidin

Dialysis of biotinylated BSA

Week 2 (May 23rd - May 29th)

Monday, May 23th

Cloning of A3C5 and Avi-Tag into pSB1C3

Filtration of Streptavidin and precipitation with Ammonium-sulfate

Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam

Retransformation of Biobricks in XL1-blue

Tuesday, May 24th

Inoculation of pre-culture with BioBricks in pSB1C3 in LB-Cam

Cloning of A3C5 and Avi-Tag into pSB1C3

Ammonium sulfate precipitation

MiniPrep of BioBricks in pSB1C3 (inoculated on May 23th)

Sequencing of P23 (weak RBS), P24 (double terminator) & P24 (Tet repressed GFP)

Wednesday, May 25th

Inoculation of pre-culture with tet-repressed GFP (P25) in LB-Cam

MiniPrep of K747096, I14033, R0040, B0015, K577893 and B0032

PCR of P19 (QC EspP) with O3 and O4

Digestion of PCR of EspP (P19 with O3 and O4)

Sequencing of P26 (CMV promotor), P27 (p cat promotor), P28 (Tet repressible promotor), P30 (Tet repressed GFP)

Ion exchange chromatography of eGFP

Thursday, May 26th

Inoculation of cultures with XL-1 F11 and F12 clones

Cloning of ligation F14 +F13

Transformation of Biobrick B0034 in XL1-blue

Transformation of Biobricks K577895 and K577894 in XL1-blue

SDS-PAGE of eGFP-fractions after IEC

Friday, May 27th

Inoculation of pre-cultures with B0034 (strong RBS), K577894 (Tet repressed YFP), KK577895 (Tet repressed RFP), F13+F14

Inoculation of BL21 (pASK75 (SA1)) culture in 2 L TB-Medium and induction of streptavidin production by addition of tetracycline

Re-sequencing of P30 (Tet repressed GFP in pSB1C3)

Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium

Cloning of A3C5 and Avi-Tag into pSB1C3

Cloning of A3C5 and Avi-Tag into pSB1C3

Week 3 (May 30th - June 5th)

Monday, May 30th

Cloning of A3C5 and Avi-Tag into pSB1C3

Religation of F13 (digest of pSB1C3 with AgeI and NgoMIV) and transformation in XL1 blue

Inoculation of pre-cultures with B0034 (strong RBS), K577894 (TET repressed YFP), KK577895 (Tet repressed RFP), F13+F14

Tuesday, May 31th

Dialysis of eGFP

Expression and harvest of Streptavidin (pASK75 (SA1)) in BL21 in TB-medium