Difference between revisions of "Team:Paris Saclay/Notebook/September/9"

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All PCR products were at the good size and seemed to be concentrated. It could be explained as these clones were grown for 2 days. Clones 7, 9, 15 and 16 were selected and were grown at 37°C overnight.  
 
All PCR products were at the good size and seemed to be concentrated. It could be explained as these clones were grown for 2 days. Clones 7, 9, 15 and 16 were selected and were grown at 37°C overnight.  
  
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====PCR on GFP 1.9 in pUC19, gblock 1.1, gblock 1.2, gblock 2.1 and gblock 2.2 with 3% DMSO ====
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As no colonies were obtained after one night culture, a new Gibson was performed with cleaned up PCR products FRB from clone 9 (insert) x pSB1C3 - GFP 11 from clone 8 (plasmid) (obtained the 6th september) with the following protocol.
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Concentration of insert and plasmid were determinated again by Nano drop. For each 20μl of reaction, mix the following reagents :
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* 0.65 µL of insert
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* 1.1 µL of plasmid
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* 8,25 µL of water
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* 10 µL of buffer mix
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Two controls were done: one without insert and one without buffer (water was added in order to have a total of 20 µL). Two different buffer mix were tested (the usual one and another one from Philippe). The PCR was performed as follow : 1 hour at 50°C.
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====Transformation of DH5a cells with FRB - GFP 11 in pSB1C3 obtained by Gibson====
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''By Maxence''
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Dh5a cells were transformed with pSB1C3 containing FRB - GFP 11, or containing controls (no buffer mix and plasmid alone) using the usual [[Team:Paris_Saclay/Experiments#heat-shocktransformation|protocol]]. As mentioned before, two buffer mix were used. Furthermore, two different DH5a strains were tested (the usual one and another one from Philippe) and at least 12 transformants were cultured overnight : 3 (1 Gibson and 2 controls) x 2 buffer mix x 2 DH5a strains.
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====Q5 PCR on FKBP in pJET and gblock 2.2 (part of dCas9 NM - GFP 10) for new clonage strategy ====
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''By Maxence''
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An other clonage strategy was performed by using Gibson between FKBP, gblock 2.2 (part of dCas9 NM - GFP 10) and pSB1C3 (the one from dCas9 ST - GFP 11) in order to have FKBP - GFP 10 in pSB1C3. For that purpose, Q5 PCR was performed on plasmids with the following protocol.
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For each 50μl of reaction, mix the following reagents :
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* 1 µL of plasmid
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* 1 µL of dNTPs (10mM)
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* 2.5 µL of each primer mix (10µM)
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* 10 µL of Q5 buffer (5X)
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* 0,5 µL of Q5 high fidelity polymerase
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* 32,5 µL of nuclease free water
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Mix gently and aliquot 50 μl of the mix into the PCR tubes on ice.
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Perform PCR as follow:
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{| class="wikitable"
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!Step
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!Temperature
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!Time
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|Initial denaturation
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|98°C
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|30sec
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|rowspan="3"|30 cycles
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|98°C
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|10sec
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|Tm
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|20sec
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|72°C
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|t
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|Final Extension
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|72°C
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|2min
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|Hold
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|4°C
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|$\infty$
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|}
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[[Team:Paris_Saclay/Experiments#primers|Primers]] used were:
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{| class="wikitable"
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!Matrix
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!gblock FKBP in pJET clones 3, 4 and 5
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!gblock 2.2 in pUC19
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|Primers
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|iPS145 and iPS146
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|iPS147 and iPS84
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|Tm
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|62°C
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|70°C
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|t
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|15 sec
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|15 sec
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|}
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====PCR on GFP 1.9 in pUC19 with 3% DMSO ====
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''By Maxence''
 
''By Maxence''
  
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As the annealing temperature (Tm) seems to high to obtain good results for GFP 1.9 in pUC19 amplification, DMSO was used in order to reduce the annealing temperature during the PCR. For that purpose, PCR was performed on plasmids with the following protocol.
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As the annealing temperature (Tm) seems too high to obtain good results for these amplifications, DMSO was used in order to reduce the annealing temperature during the PCR. For that purpose, PCR was performed on plasmids with the following protocol.
  
 
For each 50μl of reaction, mix the following reagents :
 
For each 50μl of reaction, mix the following reagents :

Revision as of 18:00, 13 September 2016

Friday 9th September

Lab work

Visualization

Colony PCR of 16 clones containing FRB - GFP 11 in pSB1C3

Maxence

Colonies were obtained for the Gibson done the 7th September but not for the one done the 8th September. A colony PCR was done for 16 clones from the 7th September. For that purpose, 16 were screened and used for the usual protocol of Colony PCR. The same colonies were also plated on Petri dish containing solid LB + 30 µg/mL Cm and liquid cultures (LB + 30 µg/mL Cm) were made from these clones. Both petri dishes and liquid cultures were grown at 37°C.

For each clones contained in 20 μl water, 4.13 μL of the following mix were added :

  • 2.5 µL DreamTaq Buffer
  • 0.5 µL of dNTPs (10mM)
  • 1 µL of each primer mix (10µM)
  • 0.13 μl of DreamTaq Pol

PCR was performed as follow:

Step Temperature Time
Initial denaturation 95°C 3 min
30 cycles 95°C 30 sec
Tm 30 sec
72°C t
Final Extension 72°C 7 min
Hold 4°C $\infinity\$ 
Primers used were:
Matrix Clones containing FRB - GFP 11 in pSB1C3
Primers iPS83 and iPS84
Tm 61°C
t 1 min 30

After amplification, 3 µL of each PCR products and 5 µL of DNA ladder were placed in wells and migrated at 100V during 30 min.

PCR products expected were :

PCR products Expected band size (bp)
FRB - GFP 11 in pSB1C3 730

GEL 6

All PCR products were at the good size and seemed to be concentrated. It could be explained as these clones were grown for 2 days. Clones 7, 9, 15 and 16 were selected and were grown at 37°C overnight.

PCR on GFP 1.9 in pUC19, gblock 1.1, gblock 1.2, gblock 2.1 and gblock 2.2 with 3% DMSO

By Maxence

As the annealing temperature (Tm) seems too high to obtain good results for these amplifications, DMSO was used in order to reduce the annealing temperature during the PCR. For that purpose, PCR was performed on plasmids with the following protocol.

For each 50μl of reaction, mix the following reagents :

  • 1 µL of plasmid
  • 1 µL of dNTPs (10mM)
  • 2.5 µL of each primer mix (10µM)
  • 10 µL of buffer (5X)
  • 0,5 µL of Phusion polymerase
  • 31 µL of nuclease free water
  • 1.5 µL of DMSO

Mix gently and aliquot 50 μl of the mix into the PCR tubes on ice. Perform PCR as follow:

Step Temperature Time
Initial denaturation 98°C 30sec
30 cycles 98°C 10sec
Tm 30sec
72°C t
Final Extension 72°C 2min
Hold 4°C $\infty$ 
Primers used were:
Matrix gblock 2.2 in pUC19
Primers iPS140 and iPS84
Tm 60°C
t 30 sec

PCR Clean-up of PCR products

By Maxence

PCR products obtained were cleaned up by using the NucleoSpin Gel and PCR Clean-up kit protocol.

NanoDrop Measurements

By Maxence

Sample Concentration (ng/µL)
PCR fragment FKBP clone 3
 222.57
PCR fragment FKBP clone 4
 219.99
PCR fragment FKBP clone 5
 376.2
PCR fragment gblock 2.2
 276.33

Gel of cleaned up PCR products

By Maxence

After amplification, 3 µL of each cleaned up PCR products and 5 µL of DNA ladder were placed in wells and migrated at 100V during 30 min.

PCR products expected were :

PCR products Expected band size (bp)
FKBP X
gblock 2.2 X
GFP 1.9 862

GEL 4 : FKBP

All PCR products were at the good size.

GEL 5 : gblock 2.2

The PCR product was at the good size.

GEL 6 : gfp 1.9