Difference between revisions of "Team:Paris Saclay/Notebook/August/3"

(Tuesday 3st August)
(High fidelity Q5 PCR on DH5alp|pPS16_004, DH5alp|pPS16_006 and DH5alp|pPS16_007)
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The bacteria transformed with the plasmids sent the 2/08/2016 and those that would be sent the 4/08/2016 were put into glycerol. 1mL of liquid culture and 0.5mL of glycerol were put at -20°C.
 
The bacteria transformed with the plasmids sent the 2/08/2016 and those that would be sent the 4/08/2016 were put into glycerol. 1mL of liquid culture and 0.5mL of glycerol were put at -20°C.
  
==== High fidelity Q5 PCR on DH5alp|pPS16_004, DH5alp|pPS16_006 and DH5alp|pPS16_007 ====
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==== High fidelity Q5 PCR on pPS16_004, pPS16_006 and pPS16_007 ====
 
''By Caroline''
 
''By Caroline''
  
Q5 PCR was carried out following the usual [[Team:Paris_Saclay/Experiments#Q5PCR|protocol]] adapted to 50µL at a TM of 72°C. The [[Team:Paris_Saclay/Experiments#primers|primers]] used were specific to amplify only the interested sequence.
+
Q5 PCR was carried out following the usual [[Team:Paris_Saclay/Experiments#Q5PCR|protocol]] adapted to 50µL at a TM of 72°C. The [[Team:Paris_Saclay/Experiments#primers|primers]] used were specific to amplify only the interested sequence. The products were put to migrated on a 0.8%agarose gel with BET. Only, PCR form pPS16_004 and pPS16_007 showed a positive result.
  
 
==== Extraction of the plasmids containing gBlocks pPS16_001, pPS16_002, pPS16_003, FRB, sg-ST1, FKPB, DS-NMcasN-, spacer and detection ====
 
==== Extraction of the plasmids containing gBlocks pPS16_001, pPS16_002, pPS16_003, FRB, sg-ST1, FKPB, DS-NMcasN-, spacer and detection ====

Revision as of 13:59, 5 August 2016

Wednesday 3st August

Lab work

Visualization

Glycerol stocks

By Caroline

The bacteria transformed with the plasmids sent the 2/08/2016 and those that would be sent the 4/08/2016 were put into glycerol. 1mL of liquid culture and 0.5mL of glycerol were put at -20°C.

High fidelity Q5 PCR on pPS16_004, pPS16_006 and pPS16_007

By Caroline

Q5 PCR was carried out following the usual protocol adapted to 50µL at a TM of 72°C. The primers used were specific to amplify only the interested sequence. The products were put to migrated on a 0.8%agarose gel with BET. Only, PCR form pPS16_004 and pPS16_007 showed a positive result.

Extraction of the plasmids containing gBlocks pPS16_001, pPS16_002, pPS16_003, FRB, sg-ST1, FKPB, DS-NMcasN-, spacer and detection

By Laetitia

The extraction was performed without kit, following the usual protocol.

It was done on:

Puc 19 containing Clone
pPS16_001 4
pPS16_002 3
pPS16_003 2, 5
FRB 5
sg-ST1 2, 3, 5
DS-NMcasN- 3
FKBP 4
Spacer 1, 6
Detection 3, 4, 6

Extraction of the plasmids containing gBlocks

By Naiane

The kit "Charge Switch-Pro Plasmid Miniprep" was used to extract plasmidic DNA of the plasmid pPS16_003 containing the Gblock 2.1, plasmid pPS16_004 containing the Gblock 2.2, plasmid pPS16_006 containing the Gblock 3.2 and the plasmid pPS16_007 containing the Gblock 4.1 from 3mL of overnight culture. Plasmids were resuspended in 100μL of Milli-Q water. DNA stored at -20°C.

Interlab Study

Preculture of device one transformed DH5a

By Lea

Two colonies were inoculated inside of two tubes of 3mL of liquid LB medium containing 30 µg/ml Chloramphenicol. The tubes were incubated at 37°C overnight.