Difference between revisions of "Team:Paris Saclay/Notebook/September/19"

(Monday 19th September)
Line 4: Line 4:
 
==Lab work==
 
==Lab work==
 
===Visualization===
 
===Visualization===
 +
 +
==== Glycerol stocks of clones 7, 8, 9 and 10 containing FKBP - GFP 10 in pSB1C3 ====
 +
"By Maxence, Mahnaz Coline & Caroline"
 +
 +
The glycerol stock of the bacteria with the following plasmids were made.
 +
*X (FKBP - GFP 10) clone 7
 +
*X (FKBP - GFP 10) clone 8
 +
*X (FKBP - GFP 10) clone 9
 +
*X (FKBP - GFP 10) clone 10
 +
 +
500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C.
 +
 +
====Plasmids extraction of clones 7, 8, 9 and 10 containing GFP 1.9 in pSB1C3====
 +
"By Maxence, Mahnaz Coline & Caroline"
 +
 +
The following plasmids were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit:
 +
*X (FKBP - GFP 10) clone 7
 +
*X (FKBP - GFP 10) clone 8
 +
*X (FKBP - GFP 10) clone 9
 +
*X (FKBP - GFP 10) clone 10
  
 
====PCR of pSB1C3 from dCas9 ST - GFP 11 clone 8 to correct mutations ====
 
====PCR of pSB1C3 from dCas9 ST - GFP 11 clone 8 to correct mutations ====

Revision as of 10:17, 19 September 2016

Monday 19th September

Lab work

Visualization

Glycerol stocks of clones 7, 8, 9 and 10 containing FKBP - GFP 10 in pSB1C3

"By Maxence, Mahnaz Coline & Caroline"

The glycerol stock of the bacteria with the following plasmids were made.

  • X (FKBP - GFP 10) clone 7
  • X (FKBP - GFP 10) clone 8
  • X (FKBP - GFP 10) clone 9
  • X (FKBP - GFP 10) clone 10

500µL of liquid culture and 250 µL of glycerol 60% were mixed and put at -20°C.

Plasmids extraction of clones 7, 8, 9 and 10 containing GFP 1.9 in pSB1C3

"By Maxence, Mahnaz Coline & Caroline"

The following plasmids were extracted using the "Charge Switch-Pro Plasmid Miniprep" kit:

  • X (FKBP - GFP 10) clone 7
  • X (FKBP - GFP 10) clone 8
  • X (FKBP - GFP 10) clone 9
  • X (FKBP - GFP 10) clone 10

PCR of pSB1C3 from dCas9 ST - GFP 11 clone 8 to correct mutations

By Maxence

In order to correct mutations in dCas9 ST - GFP 11, PCR was performed with the following protocol.

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

  • 1 µL of matrix
  • 1 µL of dNTPs (10mM)
  • 2.5 µL of each primer mix (10µM)
  • 10 µL of buffer HF (5X)
  • 0,5 µL of Phusion polymerase
  • 32.5 µL of nuclease free water

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
72°C 30sec
72°C t
Final Extension 72°C 5min
Hold 4°C $\infty$
Primers used were:
Matrix dCas9 ST - GFP 11 clone 8 dCas9 ST - GFP 11 clone 8
Primers iPS174 and iPS175 iPS173 and iPS176
Tm 72°C 72°C
t 3min 50sec