(→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 | + | ==== 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