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

(Visualization)
Line 15: Line 15:
  
 
Each PCR Product was put to migrate on an agarose gel.
 
Each PCR Product was put to migrate on an agarose gel.
 +
10µL of blue ladder was used, and the wells were filled with 1µL of PCR preparations.
 +
 +
PCR products expected were :
 +
{| class="wikitable"
 +
|-
 +
!'''Plasmid'''
 +
!pPS16_001
 +
!pPS16_002
 +
|-
 +
!'''Band Size (bp)'''
 +
|1007
 +
|1007
 +
|}
  
 
===Biobrick Characterization===
 
===Biobrick Characterization===

Revision as of 15:09, 28 July 2016

Thursday 28th July

Lab work

Visualization

Low Fidelity DreamTaqPCR of DH5a|pPS16_001, DH5a|pPS16_002, DH5a|pPS16_005 and DH5a|pPS16_009

By Mathilde and Laetitia

PCR was performed on 6 clones for each plasmid.

Thus, the PCR mix was done for 24 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. 10µL of blue ladder was used, and the wells were filled with 1µL of PCR preparations.

PCR products expected were :

Plasmid pPS16_001 pPS16_002
Band Size (bp) 1007 1007

Biobrick Characterization

BL21 electrocompetent cells in glycerol stock

By Charlène

1 mL of each clone cultured yesterday were put in 500µL of glycerol 60%. They were conserved at -30°C.