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

(Low Fidelity DreamTaqPCR of DH5alpha transformed with pPS16_005 and pPS16_009)
(Low Fidelity DreamTaqPCR of DH5alpha transformed with pPS16_005 and pPS16_009)
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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 [[Team:Paris_Saclay/Experiments#Polymerase_chain_reaction|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.

Revision as of 10:01, 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.