Difference between revisions of "Team:Paris Saclay/Notebook/August/4"

(Thursday 4st August)
(Visualization)
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The purification was carried out on DH5alp|pPS16_003, DH5alp|pPS16_004 and DH5alp|pPS16_007 following the usual [[Team:Paris_Saclay/Experiments#Purification|protocol]]. But, I forgot to dilute the sample with the Buffer NT3 with 100mL ethanol befor I began the purification and so no DNA was present on the 0.8% agarose gel.   
 
The purification was carried out on DH5alp|pPS16_003, DH5alp|pPS16_004 and DH5alp|pPS16_007 following the usual [[Team:Paris_Saclay/Experiments#Purification|protocol]]. But, I forgot to dilute the sample with the Buffer NT3 with 100mL ethanol befor I began the purification and so no DNA was present on the 0.8% agarose gel.   
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==== pPS16_004, pPS16_006 and pPS16_007 ====
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''By Caroline''
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Q5 PCR was carried out following the usual [[Team:Paris_Saclay/Experiments#Q5PCR|protocol]].
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[[File:T--Paris_Saclay--160804_gel_pcr.jpg|400px|thumb|right|Result of the PCR]]
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{{Team:Paris_Saclay/notebook_footer}}
 
{{Team:Paris_Saclay/notebook_footer}}

Revision as of 10:03, 22 August 2016

Thursday 4th August

Lab work

Visualization

DNA Extraction of pPS16_001, pPS16_002, pPS16_003, pPS16_009,DS-NMcasN-, DS-TDcasN-, DS-SPcasN-

By Caroline, Naiane, Mathilde and Laetitia


Extraction was done on:


Puc 19 containing Clone
pPS16_001 2, 9
pPS16_002 4, 7, 11
pPS16_009 7
pPS16_003 4
DS-NMcasN- 7, 11
DS-TDcasN- 1
DS-SPcasN- 1


The extraction was performed using the ChargeSwitch-Pro Plasmid MiniPrep kit from Invitrogen. We followed this protocol.

Stock of glycerol for pPS16_001, pPS16_002, pPS16_003, pPS16_009 and DS-NMcasN-

By Naiane, Mathilde and Laetitia

Stocks of glycerol were made with:

  • 700 µL of culture
  • 300 µL of glycerol (60%)

PCR Clean-up with the NucleoSpin kit

By Caroline

The purification was carried out on DH5alp|pPS16_003, DH5alp|pPS16_004 and DH5alp|pPS16_007 following the usual protocol. But, I forgot to dilute the sample with the Buffer NT3 with 100mL ethanol befor I began the purification and so no DNA was present on the 0.8% agarose gel.

pPS16_004, pPS16_006 and pPS16_007

By Caroline


Q5 PCR was carried out following the usual protocol.

Result of the PCR