Difference between revisions of "Team:SUSTech Shenzhen/Notebook/Molecular"

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(without purification), 20μl, 30 cycles
 
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2. PCR  
 
2. PCR  

Revision as of 00:35, 16 October 2016

Team SUSTC-Shenzhen

Molecular Experiment

Notebook

Contents

2015

Dec.

13th

Geco plasmid construction

1. Polymerase Chain Reaction (PCR)

Use PBX-084 TRE-mCherry-2A-Bla plasmid as template to get blasticidin(Bla) resistance gene.

Primers: Age-Bla-S & Bla-E2A-AS

(without purification), 20μl, 30 cycles

Volume/ul
Buffer 2
Template 0.5



2. PCR

Use PBX-084 TRE-mCherry-2A-Bla plasmid as template to get 2A sequence.

Primers: E2A-S & E2A-Hind III-AS

(without purification), 20μl, 30 cycles

416x184px

3. PCR

Step 1: run 10 cycles without primer to let Bla and 2A link together.

401x155px

98℃ 10s \
55℃ 5s x10 cycles
72℃ 30s /

Step 2:add primers to run 30 cycles.

Primers: AgeI-Bla-S 0.3μM & E2A-HindIII-AS 0.3μM

98℃ 10s \
55℃ 5s x30 cycles
72℃ 30s /

4. PCR product cycle purification by using E.Z.N.A.® Cycle Pure Kit.


15th

Geco plasmid construction

1. Digest the PCR purification product with AgeI and HindIII restriction endonuclease(RE).(37 ℃ 2 hours)

636x164px

2. Digest the Geco plasmid with BglII restriction endonuclease. (50℃ 3 hours)

632x146px3.Cycle pure the RE digestion product with the kit “xxxxxx”.

3. Cycle pure the RE digestion product with the kit “xxxxxx”.

4. Digest the purification product with HindIII restriction endonuclease. (37 ℃ 3 hours)

633x145px

5. Digest the vector plasmid with AgeI restriction endonuclease. (37 ℃ 3 hours)

631x144px

6.Add 1.5 μl BclII restriction endonuclease. (50 ℃ 3 hours)

Note: BclI and BglII have the same sticky end.

7. Gel running and Gel extraction to get the insert and vector fragments.E.Z.N.A.® Gel Extraction Kit - Spin Protocol


16th

Geco plasmid construction

1. Geco,Vector,Bla+2A Ligation with T4 DNA Ligase(Vector:Insert=1:3).

Vector (5.8 kbp): 5.5ng/μl

Bla+2A (0.45kbp): 16.8ng/μl

Geco (1.25kbp): 5.6ng/μl

578x236px

Room temperature for 10 minutes.

2. Mix&Go hyper-efficient competent cells transformation.

  • Quickly thaw: remove "Mix&Go" hyper-efficient competent cells from -80℃ freezer and water flow till 50% of the cells melt.
  • Add DNA: DNA volume is less than 1/10 volume of competent cells. (blow and suck for mixing )
  • Heat shock: heat shock at 42℃ water bath for 45s.
  • Spread the plates: remove LB(Amp+) plates from 4℃refrigerator,and spread all the bacterial on the plates. Overnight culture at 37℃ incubator (12~16hours).

Vector+Bla 2A+Geco 3 μl + competent cells 30 μl


17th

Geco plasmid construction

1. Vector+Bla 2A+Geco transformation results:

358x439px

2. Pick single clones and overnight culture.

Pick 5 single clones and use 6 ml Amp+ LB medium with 37℃ and 220 rpm shaker to overnight culture each clones.


18th

Geco plasmid construction

1. Extraction of plasmid with E.Z.N.A.® Plasmid DNA Mini Kit I Protocol.

581x209px

2. Send 5 plasmids to sequence.


29th

Piezo plasmid construction

1. Piezo backbone(PBX-123 plasmid from Prof.Huang’s lab) transformation.Mix&Go method.

Piezo backbone plasmids 2μl + competent cells 20μl


30th

Piezo plasmid construction

1. Piezo backbone transformation results:

402x443px

2. Pick single clones and overnight culture.

Pick 3 single clones and use 6 ml Amp+ LB medium with 37℃ and 220 rpm shaker to overnight culture each clones.

31th

Piezo plasmid construction

1. Extraction of plasmid with E.Z.N.A.® Plasmid DNA Mini Kit I Protocol.

577x138px

2. Piezo GPA、pTRE-3G PCR.

Piezo: 310ng/μl GPA: 444bp pTRE-3G: 376bp

584x232px

Program setting:

98℃ 10s \
55℃ 15s X 35 cycles
72℃ 30s /

3.Gel Running

289x225px

4.PCR purification.

E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

583x107px


2016

Jan.

21th

Piezo plasmid construction

1. Piezo plasmid construction design:

552x496px

2. Piezo plasmid(original) RE digestion: 37℃ 2hours

590x183px

3. Backbone PBX-123 plasmid RE digestion: 37℃ 2hours

600x192px

4. Gel running and gel extraction.

579x98px

E.Z.N.A.® Gel Extraction Kit - Spin Protocol

5. Gibson assembly:

573x251px

Incubate the mix for 1 hour at 50°C. (Gibson Assembly® Master Mix – Assembly (E2611) Method)

6. Gibson product transformation:

[[|Transformation & Competent cell recovery]

5μl gibson product + 50μl competent cells

Spread plates and overnight cultrue.


22th

Piezo plasmid construction

  1. Pick single colonies:
    pick 1 colony from control group, pick 5 colonies from piezo group.
    Add into 6ml Amp+ LB, shake at 37℃ and 220 rpm.
  2. Make Amp LB and agar.
    make two 500ml Amp+ LB medium and one 500ml Amp+ LB agar.
    pour 29 plates.
  3. Sterilization.
    We put bunch of tips and tubes for sterilization.

Piezo plasmid construction

  1. Extract the plasmids from the single colonies (1 control group and 5 PIEZO group):259x496px
  2. Gel electrophoresis of the six plasmids:400x229px

Sample 2 and Sample 4 have shown positive results, which should be tested further with PCR.

Materials sorting:

We sorted the material and put all of them into the lowermost layer of the -20℃ fridge.

314x176px Restriction enzyme and buffer ↑

317x178px PCR related materials ↑

277x155px Primer of our group ↑

281x157px Plasmid construction of our group ↑

281x265px Inner look of plasmid construction, left row is the final product. Right parts are materials from previous steps. ↑

396x222px Overall look ↑


25th

Piezo plasmid construction

  1. Sterilization:
    We put a bottle of ddH2O and bunch of tips and tubes for sterilization.
  2. PCR test for PIEZO group 2 and PIEZO group 4: Premix TaqTM (RR902A)

For each system 433x209px

Program setting:

95℃ 5min 95℃ 30s \ 55℃ 20s x35 cycles 72℃ 40s /

3. Gel running:

294x416px

The result showed that GpA had linked with backbone and piezo.

4. Pick up single colonies and colony PCR

As the result of gel electrophoresis of piezo Gibson group 2&4(yesterday,2016.1.24) missed bands of 4000, we picked up 20 single colonies to test by colony PCR. (use primers of GpA and PTRE).

The system of colony PCR (total 20 μl): Premix TaqTM (RR902A)

386x220px

Program setting:

95℃ 5min
95℃ 30s \
55℃ 20s x35 cycles
72℃ 40s /

Finally, we got 40 groups for PCR colonies (20 for GpA and 20 for PTRE).

5. Gel electrophoresis of 40 groups after PCR colonies.

467x437px

6.TRPC5 & TRPC6 &PBX-090 transformation.

We transformed these plasmids into competent cell and coated. After that, incubated at 37℃ for 16 hours.(5 plasmids onto 5 Amp plates)


26th

Piezo plasmid construction

1. Pick up single colonies

After TRPC5, TRPC6 and PBX-090 transformation, we found that there are no colony growing on PBX-090 plate. Later we knew that PBX-090 is Kanamycin resistant. We pick 1 colony from other 4 plates. Add into 5ml Amp LB, shake at 37℃.

2.PCR test 'Premix TaqTM (RR902A)

For yesterday PIEZO group 2 and PIEZO group 4(GPA verified): 433x209px

Program setting:

95℃ 5min
95℃ 30s \
55℃ 20s x30 cycles
72℃ 40s /

For yesterday PIEZO colony PCR promoter(pTRE) group 9,11,15(pTRE verified): 433x209px

Program setting:

95℃ 5min
95℃ 30s \
55℃ 20s x30 cycles
72℃ 40s /

3.Gel running of PCR product 346x376px

4.Streak plate of colony PCR9&11&15

We streaked 3 Amp plates using tips.

5.RE Digestion of PIEZO(original plasmid), PIEZO group 2,and PIEZO group 4 478x208pxPIEZO Total 20μl

PIEZO group 2(1) Total 20μl 450x196px

PIEZO group 2(2) Total 20μl 456x236px

PIEZO group 4(1) Total 20μl 458x201px

PIEZO group 4(2) Total 20μl 456x235px

Gel running results: 366x367px

Since the results out to be blurred, we decide to run gel again tomorrow.


27th

Piezo plasmid construction

1.Plasmid purification E.Z.N.A.® Plasmid DNA Mini Kit I Protocol - Spin Protocol

Plasmid purification of TRPC5 and TRPC6 from the single colonies we picked yesterday

The concentration of the plasmids: 490x187px

2.Gel electrophoresis of Restriction Enzyme Digestion product: 369x336px

Something must have been wrong!

3.Pick single colonies After we strake plate of colony PCR9&11&15, we pick 1 colony from each plate. Add into 5ml Amp LB, shake at 37℃.

4. TRPC5 T5-GFP PCR Q5® High-Fidelity 2X Master Mix(M0492S) 455x215px

We make 2 groups of 50μL PCR solution.

5. PCR purification E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

Accidentally make the centrifuge in step 8 30 seconds rather than 1 minute

Use 50μl ddH2O to elute DNA in the last process.

DNA concentration:

Group1: 21.8ng/μL

Group2: 31.6ng/μL

6. TRPC5 T5-GFP PCR(2nd) Q5® High-Fidelity 2X Master Mix(M0492S)

Because the DNA concentration in the last step was too low to conduct the following experiment, we did the TRPC5 T5-GFP PCR for the second time.

459x212px

We make 5 groups of 50μL PCR solution, and run 40 cycles.


28th

Piezo plasmid construction

1. Plasmid purification and maintenance breeding ① Plasmid purification of colony PCR9&11&15 from the single colonies we picked yesterday

Use 50μL ddH2O to elute DNA in the last process.

E.Z.N.A.® Plasmid DNA Mini Kit I Protocol - Spin Protocol

The concentration of the plasmids:

Colony PCR9 463.6ng/μl

Colony PCR11 556.1ng/μl

Colony PCR15 474.4ng/μl

② Maintenance breeding

Mix 500μL bacterial liquid with 500μL (volume fraction:50%)glycerol, and then shore at -80℃.

2. PCR purification E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

PCR purification of TPRC5 T5-GFP(2nd)

Use 80 μl Tris-HCl to elute DNA in the last process.

Finally, the concentration of DNA:

Group 1 55.8ng/μl

Group 2 68.7ng/μl

Group 3 69.2ng/μl

Group 4 71.6ng/μl

3. Mycoplasma detection

We did mycoplasma detection for the supernatant from the cell culture (step 4. Cell freezing) we collected yesterday.

a. PCR the supernatant by the primers of mycoplasma DNA.

The system of PCR (total 50μL): Q5® High-Fidelity 2X Master Mix(M0492S)

504x213px

Program setting:

95℃ 30s
98℃ 20s \
50℃ 10s x35 cycles
72℃ 100s /
72℃ 120s
4℃

b. Gel electrophoresis of PCR product.

264x301px Obviously, positive control turns out to be positive result, while negative control and the samples are negative results, so that our freezing cells are not polluted and we can store them into liquid nitrogen (big liquid nitrogen cell storage tank 3-4).

4.Restriction Enzyme Digestion(A) 547x142px

Digest the ends of TRPC5 for ligation.

Since we have the PBX123 with sticky ends of Age I and Bcl I, we should digest TRPC5 with Age I enzyme and Bcl I.

Firstly, we digest TRPC5 with Age I (activity:100%).The system (total 90μL):

Incubate at 37℃ for two hours.

Then, we digest TRPC5 with Bcl I (activity:75%).

We add Bcl I enzyme (1μL) into the final system of the first digestion. Incubate at 50℃ for six hours.

Digest the product of plasmid purification (step 1. today).

We digest the product of plasmid purification of pick up single colonies of streak plate of colony PCR group9&11&15 to test its linking.

The system (total 20μL): 447x201px

Incubate at 37℃ for two hours.

5. Gel electrophoresis of the digestion of plasmid purification product of colonies PCR 9&11&15 264x495px

As we digest the plasmid with only one enzyme, we only get linear 15k bp DNA. Obviously, group9&15 are positive.

6. Restriction Enzyme Digestion(B) and gel electrophoresis

We decide to digest the product of plasmid purification of colony PCR group 9&15 with Bam-HI and Bgl I to ensure they are exactly correct.

The system (total 20μL):

Bam HI-HF 0.2μL(activity:100%)

Bgl I 0.2μL(activity:100%)

DNA(~500ng/μL) 1.25μL

10×NEBuffer 2μL(3.1 buffer)

ddH2O 16.35μL

Incubate at 37℃ for two hours.

Gel electrophoresis of the product of digestion.

7. Restriction Enzyme Digestion purification E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

Use 30μL ddH2O to elute DNA in the last process.

TRPC5 T5-GFP 1 72.6ng/Μl

TRPC5 T5-GFP 2 71.3ng/μL

8. Restriction Enzyme Digestion E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

We digest PBX-123 with Age I to get the sticky end which can connected with TPRC5.

The system (total 50μL):

Age I-HF 2μL

DNA(~300ng/μL) 20μL(actually, we use PBX group 3.)

10×NEBuffer 5μL(CutSmart buffer)

ddH2O 23μL

Incubate at 37℃ for two hours.

9. Ligation (TRPC5 and PBX-123)

The system (total 20μL):

10×T4 DNA buffer 2μL

Vector(PBX123) 10μL(43.26ng)

TRPC5 1μL(55.26ng)

ddH2O 6μL

T4 DNA ligase 1μL

10. Transformation:

We transform the plasmid which we get in the step 9. Ligation into 25μL competent cell.

We also help Dr. Huang (our mentor) transform 3 plasmids into competent cell (each 25μL).

Then, we coat and incubate at 37℃for 16 hours.


29 th

Piezo plasmid construction

  1. Restriction Enzyme Digestion(PBX-123, Age I& Bcl I)

We digested PBX-123 with Age I to get the sticky end which can connected with TPRC5.

Then we use Bcl1 to digest.

The system (total 50μL):

Bcl I 2μL

DNA(~300ng/μL) 20μL (actually, we use PBX group 3.)

10×NEBuffer 5μL(CutSmart buffer)

ddH2O 23μL

Incubate at 50℃ for two hours.

179x358px

The result is strange. The brightest band is larger than 10000.

Still, we extract the plasmid from the brightest band. Concentration:61.8ng/μl

Gel running of restriction enzyme digestion (PIEZO Gibson Ligation from colony PCR group 9&15, BamHI Bgl II) 270x467px

The undigested ones showed more bands while digested one only showed one band which is really strange.

We ran the gel for two times and still got the same results.

3. Colony PCR (5 PIEZO Gibson colony &2 PIEZO Gibson control colony&Negative control ddH2O, PCR for GpA& PTRE)

Total 20μl

2xTaq 10μl

Template 5μl

Primer 1 1μl

Primer 2 1μl

DdH2O 3μl

Primers: GpA primers/PTRE primers

389x546px

From the results, GpA can still be seen in ddH2O. The result is so strange. We don’t know how to explain.

4.Colony PCR (12 TRPC5 Ligation colonies&dd H2O)

Total 20μl

2xTaq 10μl

Template 5μl

TRPC5 Primer 1 1μl

TRPC5 Primer 2 1μl

ddH2O 3μl

438x377px

The PCR results showed no correct one. We can’t see TRPC5 band.

The rightmost one: Digested PBX123 backbone for TRPC5 is the gel extraction from step 1(Conc. 61.8ng/μl).The band should be around 8000bp. While the result is larger than 10000bp. This indicates that the extracted plasmid is not right. </blockquote> 5. Restriction enzyme digest(PBX123 backbone for PIEZO, PIEZO, both MfeI&BamHI&PmeI)

  • PBX123 backbone for PIEZO

Total 50μl

PBX123(~300ng/μl) 35 μl

10x Buffer 5 μl

DdH2O 7 μl

MfeI 1μl

BamHI 1μl

PmeI 1μl

  • PIEZO

Total 50μl

PBX123(~570ng/μl) 20μl

10x Buffer 5 μl

DdH2O 22 μl

MfeI 1μl

BamHI 1μl

PmeI 1μl

6. Pick up single colonies

Since the results from the Colony PCR of TRPC5 ligation was not very promising, we pick up 6 colony from the plate. Add into 5ml Amp LB, shake at 37℃.

The signal colonies are picked for the PCR process to make sure that Colony PCR it self have nothing to do with the failure.


30th

Piezo plasmid construction

1. Enzyme digestion of PBX123(Age I and Bcl I for TRPC5)

PBX123(~300ng/μL) 30μL

Age I 1μL

CutSmart 5μL

ddH2O 14μL

Incubate in 37℃ for a whole night.

Add in Bcl I at 11:00, and move to 50℃.

Bcl I 1μL

Incubate in 50℃ for a 4 hours.

2. Gel electrophoresis of PBX123(Mfe I, BamH I and Pme I for piezo), PBX123(Age I and Bcl I for TRPC5) and Piezo

266x528px

The PBX123(MfeI BamHI PmeI for piezo) and Piezo(digested) on the other gel was cut off for gel extraction

The concentration of the extraction:

PBX-123 40.8ng/μL

Piezo 28.4ng/μL

3. Plasmid extraction E.Z.N.A.® Plasmid DNA Mini Kit I Protocol - Spin Protocol

Plasmid extraction from the single colonies we picked up yesterday.

The concentration of the plasmids:

TRPC5 ligation 1 378.2ng/μL

TRPC5 ligation 2 347.8ng/μL

TRPC5 ligation 3 343.3ng/μL

TRPC5 ligation 4 441.5ng/μL

TRPC5 ligation 5 438.0ng/μL

TRPC5 ligation 6 431.0ng/μL

4. TRPC5 PCR

We add in the primer of TRPC5 and try to make TRPC5 PCR from the ligation plasmid we extracted from the single colonies.

We also make two control groups, positive control group from the original TRPC5 T5-GFP plasmid we got, and negative control group from ddH2O.

rTaq premix 5μL

Templet 1μL

Primer1 0.5μL

Primer2 0.5μL

ddH2O 3μL

5. Gel electrophoresis of the PCR products and the gel extraction products.

365x381px

Nothing, even with the positive control group from the original TRPC5 T5-GFP plasmid we got, have shown the right result (some brightness around 3000bp).

6. Gibson assembly of Piezo and PBX123

Gibson Assembly® Master Mix – Assembly (E2611)

528x232px

7. Enzyme digestion of PBX123(Age I and Bcl I for TRPC5)(2nd)

PBX123(~300ng/μL) 30μL

Bcl I 1μL

3.1 5μL

ddH2O 14μL

Incubate in 50℃ for a 4 hours.

Conduct DNA extraction with Cycle-Pure Kit, use 45μL ddH2O to elute the DNA.

The DNA concentration was 92.5ng/μL.

DNA extraction 45μL

Age I 1μL

CutSmart 5μL

Incubate in 37℃ overnight.

8. Transformation

We transform the plasmids which we get in Gibson assembly into 33μL competent cell(1 gibson system and 4 control systems).

We also transform PBX090 and PBX123 to get more plasmid for further use.


31th

Piezo plasmid construction

  1. Gel electrophoresis of digested PBX123(Age I and Bcl I for TRPC5)(2nd)251x437px
  2. Colony PCR

Before colony PCR, we remove the plate of PBX123 from incubator to cold room.

We pick up 20 single colonies from the plate of Gibson group, 2 colonies from both control group 1 and 2. There are no colonies on plates of control group 3 and PBX090.

The system of colony PCR(use primers of poly A and pTRE):

Primer1 0.5μL

Primer2 0.5μL

Bacterial liquid 5μL

rTaq premix 6μL

We use original PBX123 to substitute the Bacterial liquid in positive control group 1.

We use poly A or pTRE that we get from the original PBX123 by PCR process to substitute the Bacterial liquid in positive control group 2.

We use ddH2O to substitute the Bacterial liquid in negative control group.

95℃ 30s
98℃ 10s \
50℃ 10s x30 cycles
72℃ 100s /
72℃ 120s
16℃

3. Gel electrophoresis of colony PCR (step 2.)

497x449px

503x479px

Obviously, every Gibson group are negative.

4. Enzyme digestion of PBX133(Bcl I and Age I, Nhe I, Xba I )

We suspect the availability of our Bcl I enzyme, so we digest this new backbone with another tube of Bcl I, and set a group digested by our enzyme to test its availability.

The system of digestion (by Bcl I of HW) (total 100μL):

Template(~200ng/μL) 50μL

Bcl I 5μL

NEBuffer(3.1) 10μL

ddH2O 35μL

Incubate in 50℃ for 1 hour.

The system of digestion (by Bcl I of IGEM)(total 10μL):

Template(~200ng/μL) 2.5μL

Bcl I(IGEM) 0.25μL

NEBuffer(3.1) 1μL

ddH2O 6.25μL

Incubate in 50℃ for 3.5 hours.

Conduct DNA extraction with Cycle-Pure Kit, use 50μL ddH2O to elute the DNA.

The DNA concentration was ng/μL.

The system of digestion (by Age I, Nhe I, Xba I )(total 50μL):

DNA extraction 42μL

Age I 1μL

Nhe I 1μL

Xba I 1μL

NEBuffer(CutSmart) 5μL

Incubate in 37℃ overnight.

5. Gel electrophoresis of PBX133 digested by Bcl I(after incubating for 1 hour) (step 4.)

229x496pxFrom the result we can ensure our enzyme is available.


Feb.

01 st

Piezo plasmid construction

1. Gel running of 4 enzymes digestion

193x529px 139x528px

For verification For gel extraction

574x410px

It’s easy to observe small fragments which is about 100-200bp. This indicates that the PBX133 backbone was cut.

Digestion sites: Bcl I,Age I,Nhe I,Xba I

2. Gel Extraction E.Z.N.A.® Gel Extraction Kit - Spin Protocol

We use the rest digested product to do gel extraction of cut PBX133(After 4 enzymes digested) Concentration:39.7 ng/μl

3. Transformation of enzyme digested products

360x406px2.5μl PBX133 digested by 4 enzymes, 2.5μl PBX133 digested by BclI(iGEM), 1μl PBX133 original, 2.5μl PBX133 digested by BclI(HW) with 25μl competent cells each.


14 th

TRPC5 plasmid construction

476x194px1. Enzyme digestion of TRPC5(T5-GFP and IRES-GPF)

Incubate in 37℃ for 3 hours.

2. TRPC5 PCR(T5-GFP and IRES-GPF)

476x195px 40 cycles

3. Make petro dishes.

We make 10 LB K+ petro dishes,75 Amp+ petro dishes and 14 LB petro dishes while waiting.

4. Gel electrophoresis of TRPC5

269x481px

The expected brightness (~3k bp) appeared with TRPC5 T5-GFP PCR.

But TRPC5 PCR purification group 4, which we did with the same process as TRPC5 T5-GFP PCR. Did not have the same brightness. So we decided to do another Gel electrophoresis process tomorrow.

5. PCR purification of TRPC5 PCR products (T5-GFP and IRES-GPF)

E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

The concentration of the products (diluted with 40μL ddH2O):

TRPC5 T5-GFP 105.2ng/μL

TRPC5 IRES-GPF 38.8ng/μL

6. Enzyme digestion of TRPC5 T5-GFP PCR purification product

Since we have the expected brightness (~3k bp) appeared with TRPC5 T5-GFP PCR, we carry on with the experiment. And started the enzyme digestion. Because Bcl I only have 75% activity in CutSmart buffer. So we decided to leave it overnight.

459x196px

Incubate in 50℃ for overnight.


15 th

TRPC5 plasmid construction

1. Enzyme digestion of TRPC5(T5-GFP-Age 1)

Add 2 μL Age 1 into the system of last-night enzyme digestion.

Incubate in 37℃ for 2 hours.

2. Enzyme digested product purification of TRPC5

E.Z.N.A.® Cycle Pure Kit - Centrifugation Protocol

The concentration of the products (diluted with 30μL ddH2O):

TRPC5 T5-GFP 58.8 ng/μl

3. Gel electrophoresis of used TRPC5

283x461px

As we can see, the expected brightness (~3k bp) also appeared. It means that our TRPC5 PCR purification product is no problem, while the other four T5 products which were did before all have problem. So the four can’t be used, we will go deep by using the new TRPC5 PCR purification product.

4. 569x173pxLigation of TRPC5 and PBX133 backbone T4 DNA Ligase(M0202)

Gently mix and let it in room temperature for 20 minutes.

Heat inactive at 65℃ for 10 minutes and put it in -20℃ for 4 hours.

5. Transformation of TRPC5 plasmid

596x122px

Results :

236x236px 237x247px

TRPC5-PBX133 Ligation 2 TRPC5-PBX133 Ligation 1

227x227px

PBX133 backbone

The results are not so good. There are many kinds of passible reasons which we will go to confirm one by one tomorrow.

16

TRPC5 plasmid construction =

  1. Learn to design primer from Prof. Huang.
  2. Make new Amp+ agar plate.
    Spread 12μl 50mg/ml Amp+ (sodium salt) to the plate made in Feb.24
    Put the plate to 25℃ for 3 hours
  3. Examination of experiment and propagation of 090

Amp+ New plate(2016.2.16):

601x146pxAmp+ Old plate(2016.2.14):

588x121pxAmp+ Former plate(2015):

578x54pxK+ plate(2016.2.14):

574x77pxResults:

Amp+ New plate(2016.2.16):

251x245px247x244px

TRPC5-PBX133 Ligation 1 TRPC5-PBX133 Ligation 2

249x248px 249x246px

PBX133 backbone 1 PBX133 backbone 2

249x254px

Control

Amp+ Old plate(2016.2.14):

248x244px 246x246px

TRPC5-PBX133 Ligation 1 PBX133 backbone 1

252x257px 271x256px

PBX133 backbone 2 Control

Amp+ Former plate(2015):

250x252px

TRPC5-PBX133 Ligation 1

K+ plate(2016.2.14):

253x254px 260x256px

Control 090

Discussion:

Compare new and old plate, it comes out that some is wrong with the plate for its antibiotic function.

We thinks there may be two reason for this:

1.the antibiotics is inactived.

2.there is some distribution problem in the production of plate.

3.there is some concentration issue with the antibiotic.

There is also some problem with the ligation of TPRC6 and PBX133 backbone.


17 th

TRPC5 plasmid construction

  1. To check whether Ampicillin and Kanamycin are effective
    • Add 1 μl Ampicillin solution to each LB agar plate and spread.Add 1 μl Kanamycin solution to each LB agar plate and spread.
    • 2 Let them stay for 3 hours.
    • 3 Add 25 μl competent cell to each plate. Incubate for 16 hours in 37 ℃
    Result:There is no any colony in each plate. So Ampicillin and Kanamycin are effective.
  2. TRPC5 primer design

398x501px

3. Make Amp+ and K+ LB agar plates.

We made 2*500ml LB agar. Add 500μl 1000x Amp+ in one and add 500 μl 1000x K+ in the other. We poured 15 K+ plates and 13 Amp+ plates.


18 th

TRPC5 plasmid construction

  1. Modify the previous designed primers,based on following defects
    1. Protection bases are too short,should be 4~6 bases.
    2. The temperature of matching pieces is too low,should be 55~65℃,and the Tm of primer should be 75~85℃.
    3. The number of bases between start codon and stop codon of final ligation product should be the fold of 3.
    Modified primers:

J23100-sfgfp-pBX123-piezo-primer

primer1:5'-AGAC ACCGGT TCTAGA CTAGAGTCGCGGCCGCTTTACTTGTA- 3'

AgeI XbaI Tm 62.6

primer2:5'-TACG GGATCC TTA T GGCGCGCC TTGATATCGAGCTCTTGACGGCTAGC- 3'

BamHI AscI Tm 60.9 J23100-sfgfp-pBX123-TRPC5-primer

primer1: 5'-AGAC ACCGGT GAATTC CTAGAGTCGCGGCCGCTTTACTTGTA- 3'

AgeI EcoRI Tm 62.6

primer2: 5'-TACG GGATCC TTA T GCGGCCGC TTGATATCGAGCTCTTGACGGCTAGC- 3'

BamHI NotI Tm 60.9

2. Amplify PBX-123 backbone

Backbone 1μL+competent cell 33μL (3 tubes)

Results:All 3 culture dishes don’t grow colony.

Discussion:Maybe the concentration of PBX-123 backbone is too low,so we increase the concentration.(2016.02.19)

3. Enzyme digestion of PBX-123 backbone(previous extracted PBX-123) 414x154px 2 tubes,each 3μL

Purification of PBX-123(30μL system,2 tubes)

Results:

①13.7ng/μL A260/280: 1.6

②20.6ng/μL A260/280: 1.4

4. Add Klenow Fragment to create blunt ends(2 tubes)

Klenow Fragment: 5units/μL

DNA Polymerase I, Large (Klenow) Fragment(M0210S)

Protocol(combine the NEB and Chinese protocol):

569x172px

②Incubate 15min at 25℃

③Incubate 30min at 75℃

5. Gel electrophoresis of 2 tubes blunt-ended PBX-123

Marker: DL10000

Results: Both 2 bands are near 10000bp and at the same site,which means the two bands are both blunt ends or sticky ends,we need to confirm after extracting the plasmid.

(We forgot to take a picture of the gel)

19 th

TRPC5 plasmid construction

1. Gel cutting and extraction of PBX-123 Klenow Fragment products

(30μL system)

Concentration:7.6ng/μL, A260/280: 1.55

2. Ligation of PBX-123 blunt end T4 DNA Ligase(M0202)

341x141px

Amplify PBX-123 backbone,transform,select single colony and shake colony(4 tubes)

Results:

PBX-123/ μl Competent cell/ μl Colonies
0 25 0
5 25 10+
15 25 2
25 25 1

333x249px264x302px Fig.1 PBX-123 0 μl control Fig.2 PBX-123 5 μl

337x252px340x255px

Fig.3 PBX-123 15 μl Fig.4 PBX-123 25 μl

Discussion:

The number of colonies decreases as the concentration of PBX-123

backbone increases,which is strange,so we need to do a gel running after

extracting the plasmid to confirm whether the PBX-123 has problem.

4. Ligation product transform,select single colony and shake colony (1 tubes)

Results: only one culture dish grows 1 colony

326x356px

PBX-123 Not I-cut ligation 3

---

20 th

TRPC5 plasmid construction

1. PBX123 and PBX123(NotI-cut ligation) plasmid extraction

AxyPrep Plasmid Miniprep Spin Protocol

Final volume: 70 ul each tube

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2. Breed preservation :

500ul bacterial : 500ul glycerol each tube

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3. NotI digest and transform (2 tubes)

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Purification: 40 ul system

Results: ① 18.1 ng/μL A260/280: 1.64

Transform 3 plates (Amp+)

4. He Yuhao repeats PBX123 NotI-cut:

NotI digest: 2 tubes

328x206px

Purification: 30 ul system each

Results: ① 25 ng/μL A260/280: 1.70

② 23 ng/μL A260/280: 1.66


21 th

TRPC5 plasmid construction

1.Select single colony

All 3 culture dishes grow many colonies,but we still need to do colony

PCR to confirm they are blunt-ended.Ling Shaohua has designed the primer

for colony PCR,we need to ask Pro.Huang whether it’s right.

So we select 10 colonies,each with 10ul Amp+ LB broth and store at cold

room.When the primer is verified and synthesized,we will do colony PCR

and extract plasmid from those colonies which are confirmed to be right.

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248x256px

PBX-123 Not I cut 2.20 ① PBX-123 Not I cut 2.20 ②

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PBX-123 Not I cut 2.20 ③


22 th

TRPC5 plasmid construction

1.Enzyme double digestion of HindIII-HF,Not I-HF. 37 ℃, 3hrs

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510x170px

567x436px Fig.1 PBX-123 plasmid pattern

2.Gel running, proof:

318x606px This shows we have successfully delete the Not-I RE site.

24 th

TRPC5 plasmid construction

1. TRPC5 enzyme digestion

We cut the TRPC5 PCR gel extraction from day 2.16 to give it a shot.

Only 23μL DNA left inside the tube.

523x162px

2. Transformation

We transform PBX133 PBX090 and Piezo to propagate them for further use.

We use the micropipette to inhale and blow the liquid inside Piezo for the plasmid sample, and add it to 33μL competent cells.

We add 2.5μL PBX133 and 2.5μL PBX090 to 33μL competent cells.

We coat and incubate at 37℃for 16 hours.


April

13 th~24 th

087&NFAT Plasmid Construction

Restriction Enzyme Digestion for Verification

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Gel Extraction

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Sequencing Result:

Correct

04.24~05.06 TRPC5 Plasmid Construction

06.15~06.30 Restriction Enzyme,Ligase and Transformation Efficiency Test sfgfp PCR and Gel Extraction

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Transformation Result

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July

0 1 st

Efficiency Tests

Transformation efficiency (3 groups)

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Enzyme digestion efficiency (3 groups)

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1>Prepare digestion system:

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Incubate at 37℃,6hrs.

Ligation efficiency (3 groups)

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1> Prepare ligation system T4 DNA Ligase(M0202)

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Incubate at room temperature for 20mins

Transformation & Competent cell recovery

1. Get competent cell (DH5α) from -80℃,lay on ice for 15mins till melted.

2. Add plasmids according to the table above, gently blow to mix well.

3. Incubate on ice for 30mins.

4. Incubate in 42℃ water bath for 90s.

5. Lay on ice for 5mins.

6. Add 300μl LB, 37℃, 220rpm for 20mins.

7. Add 300μl Amp+ LB, 37℃, 220rpm for 20mins.

8. Centrifuge at 5000rpm, 1min. Drop 400μl suspension.

9. Mix the left 200μl gently, spread plate.

NOTE:

  1. For ligation products, subpackage of competent cell may decrease the final efficiency.
  2. During transformation, after heat shock, competent cell should be spread on preheated agar plate (37℃) to reach a higher transformation efficiency.

02 nd

Efficiency tests results:

509x337px

NOTE:

Too many non-target bacterial colonies(non-green).

Efficiency tests failed.

Non-green colony test (I)

Pick 1 non-green colony on each plate.

Mix with 20μl ddH2O

Get 10μl add into 5ml Amp+ LB to incubate at 37℃, 220rpm for <16hrs.

Get 10μl to do colony PCR:

1> Primer

Forward -- AACGTATAAGCTTTAGGCGTGTACG

Reverse -- TTGTGCACCAGTCATAGCCGAATAG

2> Polymerase Chain Reaction (PCR)system</ul>

Q5® High-Fidelity 2X Master Mix(M0492S)

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3> PCR setting

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4> Gel electrophoresis

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03 th

Non-green colony test (II)

1. Use E.Z.N.A.TM Plasmid Mini Kit(Omega D6942-02) to purified plasmids.

According to spin protocol.

Test the concentration ( Eppendorf BioSpectrometer)

Use another pairs of primers to do PCR

Primer Forward -- CTAGAGTCGCGGCCGCTTTACTT

Primer Reverse -- TCGAGCTCTTGACAGCTAGCTCA

4.Double-enzyme digestion

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5. Gel electrophoresis

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04 th

Non-green colony test (III)

1.Enzyme digestion

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2. Gel electrophoresis

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06 th

1.Enzyme digestion

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2. Gel electrophoresis

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07 th-10 th

New plasmids design:

  • TRPC5-Loxp
  • Sfgfp-pBX123
  • pBX097-neoloxp

11 th

TRPC5-Loxp Plasmid Construction(I)

1. TRPC5-R plasmid enzyme digestion

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Gel electrophoresis for gel extraction

238x228px 254x235px

NOTE: Wrong length and faint bands

DraIII digestion site:

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12 th

TRPC5-Loxp Plasmid Construction(II)

1.TRPC5-L and TRPC5-R PCR

Primer F -- TTGGCAAAGAATTCCTCGAGG

Primer R -- GCCGATCATGCTGATATTGAGT

2.Gel electrophoresis for gel extraction

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3.Gel Extraction (According to Gel Extraction protocol )

4.TRPC5-L plasmid re-synthesis

13 th

pBX097-neoloxp construction(I)

Neoloxp PCR from pBX123 plasmid

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Gel extraction

Test product’s concentration

4.Double-enzyme digestion and pBX097 plasmid enzyme digestion

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5.Gel electrophoresis

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16 th - 21 th

pBX097-neoloxp construction(II)

1.Ligate the pBX097 and neoloxp with T4 DNA ligase and Quick Ligase (NEB)

2.DNA transformation

Result: None colony

TRPC5-Loxp Plasmid Construction(III)

TRPC5-R PCR product double-enzyme digestion (AflII; KpnI) overnight

TRPC5-L synthesis products transformation

TRPC5-L plasmid purification

TRPC5-L plasmid enzyme digestion (AflII; KpnI) overnight

Ligation of TRPC5 left and right (T4 DNA ligase)

Spread plate, incubate at 37℃ for <16hrs

Pick single colony, incubate in 15ml Amp+ LB for 16hrs at 37℃

Separate the culture into 5ml(to prove); 9.5ml(for endofree); 0.5ml (for

preservation in -80℃)

Single-enzyme digestion (PvuI; BamHI) and gel electrophoresis

426x271px

Correct

pBX123-sfGFP construction

  1. sfGFP PCR
  2. Pbx123 double-enzyme digestion

3. Double-enzyme digestion ( AgeI; BamHI ) of sfGFP Overnight

4.Gel Extraction and Cycle pure

5. Ligation of sfGFP and pBX123 backbone

6. Spread plate incubate at 37℃, <16hrs

7. Pick 8 colonies incubated in 5ml Amp+ LB each, at 37℃ 220rpm for <16hrs

8. Plasmid purification

E.Z.N.A.® Plasmid DNA Mini Kit I Protocol - Spin Protocol

9. Double enzyme digestion for proof (AflII; EcoRI)

10.Gel electrophoresis

589x231px

22 th - 23 th

pBX097-neoloxp construction(II)

1.Ligate the pBX097 and neoloxp with T4 DNA ligase and Quick Ligase (NEB)

2.DNA transformation

Result: 7 colonies

3. Pick colonies to 5ml Amp+ LB, incubate at 37℃, 220rpm for <16hrs.

4. Plasmid extraction with Plasmid Mini Kit (Omega)

5.Single-enzyme digestion

283x184px

Incubate at 37℃, overnight.

24 th - 25 th

pBX097-neoloxp construction(II)

1.Gel electrophoresis

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Result: pBX097-neoloxp successfully constructed.

26 th - 30 th

TRPC5-Loxp Plasmid Construction(IV)

1.TRPC5-Loxp endofree plasmid purification.

2.pBX097-neoloxp and TRPC5 sequencing

Primer for TRPC5---GCCGATCATGCTGATATTGAGT

Primer for pBX097-neoloxp---GGCAACGTGCTGGTTATTGTGC

Aug.

01 st - 02 nd

pBX123-sfGFP Efficiency test

388x104px

Repeat the experiments steps mentioned in 7.1

03 rd - 04 th

pBX123-sfGFP enzymes’ digestion sites ligation ability

396x73px302x171px

1> Prepare digestion system, incubate overnight

2> Gel extraction to get different fragments

3> Ligation of T4 DNA ligase/Quick ligase

4> Transformation

Results:

320x181px

05 th

TRPC5-loxp sequencing results:

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pBX097-neoloxp sequencing results:

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06 th - 07 th

Non-green colony PCR

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09 th

Change NFAT-YFP to NFAT-EGFP(I)

Double enzyme digestion (AgeI, BamHI) pBX123 to get EGFP fragment

Double enzyme digestion (AgeI, BamHI) NFAT-YFP to get backbone Overnight

10 th

Change NFAT-YFP to NFAT-EGFP(II)

Gel extraction for EGFP and NFAT backbone

Ligation by T4 DNA ligase

Transformation

11 th - 13 th

Change NFAT-YFP to NFAT-EGFP(II)

  1. Pick single colony to culture in 15ml Amp+ LB for 16hrs
  2. Plasmid mini kit to get purified plasmid
  3. Enzyme digestion to prove
  4. Send to sequencing

22 th

TRPC5 Random mutagenesis(I)

355x96px

Megaprimer PCR

1> Pre-experiments: T5 exonuclease digestion level according to time.

a. Use PrimerStar to do PCR of TRPC5 mutation region (~640bp)

b. Gel extraction to get TRPC5 mutation region

c. Set a series gradients of T5 digestion time: 0, 5, 10, 20mins

290x160px

d. EDTA preparation

To get EDTA solution with final concentration of 11mM (Planing to add 1μl solution into

50μl to stop reaction). We should get 540mM stock solution.

  • Weigh 1.08g EDTA powder add into 5ml ddH2O
    • Use magnetic stirring bar to help dissolve
      • Add NaOH powder to adjust solution’s PH until dissolved completely
        • Use 0.22μm filter to filtrate the solution
          • store in -20℃

Note: To keep T5 exonuclease digestion time as precise as possible, according to its protocol, we use EDTA to stop the digestion. e. T5 digestion (according to T5 exonuclease protocol) 262x163px f. Take group①②③for gel extraction; ④⑤⑥for cycle pure. 562x245px

23 th

Megaprimer PCR 1> Send ④⑤⑥ to sequence Primer F:ATCCGAATTCCCCTCCAAATC Primer R:TATGTTAAGTTCCCAGCCCAG 2> Megaprimer PCR:

  • Use Q5® High-Fidelity 2X Master Mix(M0492S), System 50μl, Tm=65℃
    • Cycle pure to get purified PCR products.
      • Use DpnI to digest plasmids that come from bacteria (methylated sites)

318x146px **** Transformation of digested products.

24 th

Megaprimer PCR results of different digestion time and ratios of templet and

primer:

497x611px

TRPC5 mutation region PCR

TPRC5 preserved bacteria plate streaking

DpnI digestion time experiment: “Whether 100ng plasmid can be digested completely by 1μl DpnI in 25μl, for 1h”

Result:

334x292px

25 th

Megaprimer PCR

  1. To find out the best annealing temperature for megaprimer. Set a series of annealing temperatures: 55, 60,65,70℃
  2. Repeat PCR
  3. Cycle pure to get purified PCR products.
  4. DpnI digestion
  5. Transformation

26 th

Megaprimer PCR results of different digestion time;PCR annealing temperatures and ratios of templet and primer:

530x304px

Colony number according to different annealing temperatures and ratios of templet and primer:

540x174px

Sequencing results of T5 exonuclease digestion level according to time:

527x169px


Repeat T5 exonuclease digestion level according to time:

Set series of time gradients: 0, 5, 7.5, 10mins

a. T5 digestion (according to T5 exonuclease protocol)

262x163px

b. Take each group for Gel electrophoresis

332x257px

c. Send each group to sequence

Primer F:ATCCGAATTCCCCTCCAAATC

Primer R:TATGTTAAGTTCCCAGCCCAG

28 th

Sequencing results of T5 exonuclease digestion level according to time:

559x244px

29 th

Culture medium Pollution proving:

Set 4 groups of experiments (use sfGFP plasmid):

338x110px

30 th

Culture medium Pollution proving results:

Group 3 number > Group 1 number ; with lots of non-green bacteria

Group 4 has >100 colonies of non-green bacteria

Group 2 has no colony

Conclusion: Culture medium has been polluted.

Gibson assembly (pre-experiment)

1> Directly cut the mutation region by AflII and EcoRI for 8hrs

2> Gel extraction to get the 640bp fragment

341x267px

3> Use Gibson Assembly® Master Mix to get whole plasmid

4> Transformation

31 th

1.Gibson assembly result: NONE colony

2.Random mutagenesis with Kit, according to Random mutagenesis protocol

Sept.

01 st

Design qPCR Primers and Send for Synthesization

Sequences:

1.097&NeoLoxP qPCR-1st

552x228px

2. qPCR Internal Positive Control 553x118px

04 th

Gibson Assembly

Insert : vector=2 : 3(50~100ng vector)

608x120px

T5 Exonuclease Digestion

Temperature: 50℃

472x64px

Transformation into Competent Cells

5μl product are transformed with 50ul competent cells.

Error-prone PCR(low frequency)

1. Information supplied with the GeneMorph II Random Mutagenesis Kit

(Agilent Technologies,Catalog #200550):

553x320px

2. Primers sequence:

Forward: ttactcaccatacagagatcgaattcc

Reverse: ttttccactttgctcagctccttaag

Target DNA mass: 500ng,corresponding to low frequency mutation

529x284px

4. Procedure

553x226px

The annealing temperature is set to be 57℃.

Gel Extraction of ep-PCR Product

Concentration: 135ng/μl, 30μl

qPCR Primer Test

Instrument: ABI StepOne Plus qPCR

Kit: Power SYBR® Green PCR Master Mix and RT-PCR Reagents Kit

Sample:

CHO cell genomic DNA extracted from 4.5x106 cells.

Concentration: 56.1ng/μl, 400μl

Target:

Neoloxp segment, 18sRNA, GAPDH

Standard:

097&Neoloxp plasmid(length:6635bp)

Concentration: 101.2ng/μl

616x156px

4.

611x175px

5. Procedure

669x161px

05 th

Transformation Result

No colony

Possible reason: The transformation efficiency of self-made competent cells is quite low.

06 th

TRPC5 PCR with PrimeStar

1.Primers sequence:

Forward: ttactcaccatacagagatcgaattcc

Reverse: ttttccactttgctcagctccttaag

2.Total 8 tubes of PCR reaction:

553x212px

3. Procedure

553x156px

Gel Extraction

711x226px

Concentration: 180ng/μl, 30μl, total 4 tubes.

T5 Digestion for 3.5 minutes and Cycle-pure

Concentration: 60ng/μl, 50μl

Mega-primer PCR with KOD Polymerase

Template DNA: 0.1ng,

Mega-primer:Template=10000:1

553x260px

Procedure:

553x155px

Cycle-pure and Gel Running

Concentration: 30ng/μl, 50μl

242x319px

No 6000bp band is appeared,it’s a problem!!

DpnI Digestion for 1 hour

Transformation

5μl product are transformed with 100ul competent cells.

qPCR Primer Test

Instrument: Bio-Rad

Kit: TaKaRa-One Step SYBR PrimeScript RT-PCR Kit I

1. Sample:

CHO cell genomic DNA extracted from 4.5x106 cells.

Concentration: 56.1ng/μl, 400μl

2. Target:

Neoloxp segment, 18sRNA, GAPDH

3. Standard:

097&Neoloxp plasmid(length:6635bp)

Concentration: 101.2ng/μl

612x155px

4.

608x186px

Wrong: Forget to add ‘PrimeScript Enzyme Mix’ which contains ‘Taq enzyme’,thus no PCR reaction works.

5. Procedure

669x161px

07 th

Transformation Result

No colony

Possible reason: The mega-primer PCR procedure didn’t work.

Mega-primer PCR with Q5

1.Template DNA: 0.1ng,

Mega-primer:Template=10000:1

553x164px

2. Procedure

553x155px

qPCR Primer Test with Premix and Gel Running

3. Gel concentration: 2%(to better show the needed band)

551x231px

Procedure

553x174px

4. Results

576x295px

696x187px

The gel running results show that primer 1~4 and primer GAPDH has been contaminated,we need to use new primer and be care of experiment operation.

08 th

Gel Running with 30μl mega-primer PCR product

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There is a band at around 6000bp position!

DpnI Digestion for 1 hour

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Transformation

10μl product are transformed with 100ul competent cells.

9 th

Transformation Result

Little or no colony is appeared,maybe the transformation efficiency of competent cell is still too low.

09.12 Pre-experiment of enzyme digestion and ligation

TRPC5 PCR with PrimeStar

Primers sequence

Forward Primer: atccGAATTCccctccaaatc

Reverse Primer: ATGATCTCCAGTTCTCTGGA

2. Total 2 tubes PCR reaction

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3. Procedure

553x156px

Gel Extraction

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Concentration: 44.4ng/μl, 40μl

EcoRI,SacI Restriction Enzyme Digestion

1. Insert

294x212px

The digestion is from 00:20 to 09:00.

2. Vector 300x214px

The digestion is from 21:00 to 09:00.

qPCR Primer Re-design and Send for Synthesization

Sequences:

097&NeoLoxP qPCR-2nd

622x225px

13 th

Transformation

Use the bought competent cell,with transformation efficiency of approximately 10^7.

Gel Extraction of Enzyme Digested Vector

360x360px

Concentration of vector: 44.8ng/μl,20μl

Cycle-pure of Enzyme Digested Insert

Concentration of insert: 25.3ng/μl, 40μl

Ligation with T4 DNA Ligase

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The ligation is from 12:50 to 14:00.

Transformation

14 th

Transformation Result

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516x504px

518x177px

Competent Cell Efficiency

1. Formula: Colonies on plate / ng of DNA plated x 1000 ng/μg

2. Calculation: 237 / 0.02 x 1000=1.185x107 cfu/μg

3. Actual meaning: 20pg,5640bp→3.457x106 copies

4. 457x106 / 237=14586,which means 1 of 14586 vectors would actually grow on the plate.

Ligation Efficiency

1. 62ng,4906bp→1.232x1010 copies

2. Efficiency=

Mutation Library

1.Q5: 2.782x106

2.Gibson: 5.54x105

3. Ligation: 2.102x107

Repeat the pre-experiment on 09.12

Use enzyme digestion and ligation method to construct mutation library,except that using error-prone PCR,and the target DNA is 500ng.

461x331px

334x302px

15 th

qPCR Primer Test with Premix and Gel Running

1. Procedure is the same with the experiment on 09.07

2. Results:

755x188px

2. Conclusion:

I. Primer 1~4 are not good enough,cause they all can match with CHO cell’s gDNA and have PCR products.

II. Primer 2~4 are contaminated.

III. Primer GAPDH has unspecific PCR product,so it can’t be used.

Primer 18sRNA can be used.

18 th

Transformation

10μl positive ligation product are transformed with 125ul competent cells.For control group,5ul ligation product are transformed with 50ul competent cells.

qPCR Primer Test with Premix and Gel Running

1. We set 2 annealing temperature,which are 65℃ and 70℃ respectively.

2. Results:

865x276px3. Conclusion:

I. Primer 1~4 are all not contaminated and have specific PCR band with annealing temperature of 65℃,while they don’t have PCR product band with annealing temperature of 70℃.

II. Raising annealing temperature can reduce unspecific amplification,while it can also decrease the PCR efficiency and cause Ct increasement.Also we need to verify whether the product band is what we need.

19 th

Transformation Result

330x57px

1. Mutation library(10ul ligation product)=10688

2. Ligation efficiency=

Pick 20 Single Colony for sequencing

Sequencing Result:

7 out of 20 plasmids have mutation(s) among specific region,in which one has 15 base mutations,one has 2 base mutations,and the rest five have 1 base mutation.

Scrape the Colonies for Endo-free Plasmid Extraction

The scraped colonies are cultured for around 9 hours till the OD achieves 2.879,with 150ml Amp.

Concentration: 55ng/μl, 1.75ml

20 th

qPCR Primer Test with Premix and Gel Running

1. We set 3 annealing temperature,which are 61℃,62℃ and 63℃ respectively.

2. Results:

621x618px

21 th

CHO cell Genomic DNA Extraction

Positive: GECO+NFAT+Neoloxp

①d1-A10 ②d2-B5 ③d2-B9 ④d1-D3 ⑤d2-E9

⑥d1-F5 ⑦d1-F11 ⑧d1-A9 ⑨d1-B3 ⑩d2-C1

Control: GECO+NFAT

①C4 ②E6 ③F8 ④H10

22 th

qPCR Primer Test

Instrument: ABI StepOne Plus qPCR

Kit: TaKaRa-One Step SYBR PrimeScript RT-PCR Kit II

1. Sample:

CHO cell genomic DNA

Positive: transfected with GECO+NFAT+Neoloxp

Negative Control: transfected with GECO+NFAT

Wild Type Control: CHO cell genomic DNA

2. Target:

Neoloxp segment, 18sRNA

3. Standard:

097&Neoloxp plasmid(length:6635bp)

Concentration: 101.2ng/μl

612x149px

4.

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5. Procedure

671x158px

6. Results 314x157px Conclusion

I.Can’t use ‘TaKaRa-One Step SYBR PrimeScript RT-PCR Kit II’,cause our sample is DNA.

II.We forgot to add ‘PrimeScript Enzyme Mix’ at the beginning,which may cause inaccurate results.

III.We forgot to change pipette tips during the dilution,which may bring huge deviation.

IV.Two-step PCR has a low amplification efficiency in our experiment.To increase the efficiency,we need to use three-step PCR.

23 th

qPCR Primer Test

Instrument: ABI StepOne Plus qPCR

Kit: TaKaRa-SYBR Premix Ex Taq II(Tli RNaseH Plus)

1. Sample,Target and Standard are the same with the experiment yesterday.

2.

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3. Procedure 650x146px 4. Results 332x143px 471x117px 5. Conclusion

Primer 3,4 are similarly efficient,combining with previous experiment result,we choose Primer 3 in the later experiment.

24 th

Repeat the mutation experiment on 09.14

1. The targeted mutation segments are 1ng,10ng,100ng respectively.

2. During the first PCR procedure,the annealing temperature is set to be 52℃,which is quite low,so it didn’t work.Then we change it to 57℃.

3. Procedure

553x172px

Gel Extraction of PCR Product(as Insert)

553x55px

Each with volume of 30μl.

EcoRI,SacI Restriction Enzyme Digestion for 9 hours

Cycle-pure

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qPCR Primer Test with Premix and Gel Running

Annealing temperature: 62℃

543x192px

Conclusion:

I.We can directly see the band’s brightness differences from the gel running result,which may indicate their plasmid copy number differences.Still,we need to do quantitative PCR to get more precise results.

II.It’s strange as well as unreasonable that band appears in wild-type control PCR result,which may indicate that it has been contaminated.

qPCR: 097-gDNA with Primer3

Instrument: ABI StepOne Plus qPCR

Kit: TaKaRa-SYBR Premix Ex Taq II(Tli RNaseH Plus)

Sample: Positive ①②③⑤⑦⑧⑩

Target: Neoloxp

Standard: 097&Neoloxp plasmid-③

2. Reagent and Procedure are the same with the experiment on 09.23.

3. Results

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4. Conclusion

Wild type control(new) may be contaminated.

25 th

We find that the synthesized TRPC5 has a problem,which may cause replacement during protein translation,so we need to re-construct TRPC5 plasmid.

Primer Synthesization(send to Invitrogen)

Sequences

Forward Primer: atccGAATTCccctccaaatc(we already have,don’t need to synthesize)

Reverse Primer: tgc tctaga gtg gcccagctgtactacaag

26 th

qPCR Primer Verification with Premix and Sequencing

Sequencing Results:

The PCR results are what we need,and the wild-type genomic DNA which were recently extracted are indeed contaminated.

27 th

Re-construct TRPC5 Plasmid

TRPC5 PCR with modify-primer

Same procedure as before

Gel Extraction

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XbaI,SacI Restriction Enzyme Digestion for Vector and Insert

28 th

Gel Extraction for Vector

Cycle-pure for Insert

T4 DNA Ligation for 20min

Transformation

After culture for 10 hours:

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Pick 8 Single Colony and Culture for Sequencing

Sequencing Result:

All correct.

Culture Colonies for Endo-free Plasmid Extraction

CHO Cell Genomic DNA Extraction

Positive: GECO+NFAT+Neoloxp

(11)d1-C1 (12)d1-C8 (13)d1-D12 (14)d1-E3 (15)d1-E4

(16)d1-F3 (17)d1-F6 (18)d1-F9 (19)d2-C3 (20)d2-C8

(21)d2-D5

29 th

PvuI,NcoI Restriction Enzyme Digestion for Verification

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Verification result: All correct.

Oct.

01 st

Construct Mutation Library

Vector: TRPC5 digested with EcoRI,SacI,AflII

Insert: ep-PCR segments,with low&medium&high mutation frequency.

Gel Extraction of Enzyme-digested Vector

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Ligation for 1 hour

Transformation

5μl ligation product are transformed with 100ul competent cells.

qPCR: 097-gDNA with Primer3

Instrument: ABI StepOne Plus qPCR

Kit: TaKaRa-SYBR Premix Ex Taq II(Tli RNaseH Plus)

1. Sample: Positive (3),(11)~(21)

Negative: wild type cho cell gDNA

Target: Neoloxp

Standard: 097&Neoloxp plasmid( Endofree-① ),289ng/μl

The first and last dilution point are added with 10ng wild-type gDNA,to see its influence on standard curve.

2. Reagent and Procedure are the same with the experiment on 09.23,except that the annealing temperature is set to be 64℃.

3. Results

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4. Conclusion

I. The plasmid concentration differs each time,we need to standardize the method for concentration measurement.

II. The primer is not good enough,which may cause inaccurate standard curve and copy number result.

02 nd

Scrape the Plate for Endo-free Plasmid Extraction

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Each with volume of 100μl.

CHO Cell Genomic DNA Extraction

Positive: GECO+NFAT+Neoloxp

d2-C6 (23)d2-A5 (24)d2-A8

d2-A9 (26)d1-D10 Wild type: CHO cell’s gDNA All the plasmids’ concentrations are re-measured using NanoDrop.

03 rd

qPCR: 097-gDNA with Primer3

Instrument: ABI StepOne Plus qPCR

Kit: TaKaRa-SYBR Premix Ex Taq II(Tli RNaseH Plus)

1. Sample: Positive (3),(22)~(26)

Negative: wild type cho cell gDNA(newly extracted)

Target: Neoloxp

Standard: 097&Neoloxp plasmid( Endofree-① , 307.8ng/μl

All the dilution points are added with 10ng wild-type gDNA.

2. Reagent and Procedure are the same with the experiment on 09.23,except that the annealing temperature is set to be 64℃.

3. Results

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4. Conclusion

I. The standard curve efficiency is 140%,it may result from the adding of wild type gDNA in the preparation of standard point.

II. The Ct of wild type gDNA is 26,which indicates that it has been contaminated.So the copy number results are not precise,we can only compare their differences.


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