Difference between revisions of "Team:Paris Saclay/Notebook/July/28"

(Low Fidelity DreamTaqPCR of DH5alpha transformed with pPS16_005 and pPS16_009)
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''By Laetitia ''
 
''By Laetitia ''
  
PCR was performed on 6 clones for DH5a|pPS16_005 and 6 clones for DH5a|pPS16_009.
+
PCR was performed on 6 clones for DH5a|pPS16_005 and 6 clones for DH5a|pPS16_009.  
 +
 
 
Thus, the PCR mix was done for 12 tubes following the usual protocol.
 
Thus, the PCR mix was done for 12 tubes following the usual protocol.
 +
 
Each clone was taken off from the petri dish (27/07) soaked in a PCR mix and finally re-plated on a Petri dish (LB+AMP+X-Gal+IPTG.
 
Each clone was taken off from the petri dish (27/07) soaked in a PCR mix and finally re-plated on a Petri dish (LB+AMP+X-Gal+IPTG.
 +
 
PCR was done with a Tm at 57°C.
 
PCR was done with a Tm at 57°C.
 +
 
Each PCR Product was put to migrate on an agarose gel.
 
Each PCR Product was put to migrate on an agarose gel.
  
  
 
{{Team:Paris_Saclay/notebook_footer}}
 
{{Team:Paris_Saclay/notebook_footer}}

Revision as of 10:00, 28 July 2016

Thursday 28th July

Lab work

Visualization

Low Fidelity DreamTaqPCR of DH5alpha transformed with pPS16_005 and pPS16_009

By Laetitia

PCR was performed on 6 clones for DH5a|pPS16_005 and 6 clones for DH5a|pPS16_009.

Thus, the PCR mix was done for 12 tubes following the usual protocol.

Each clone was taken off from the petri dish (27/07) soaked in a PCR mix and finally re-plated on a Petri dish (LB+AMP+X-Gal+IPTG.

PCR was done with a Tm at 57°C.

Each PCR Product was put to migrate on an agarose gel.