Difference between revisions of "Team:Paris Saclay/Notebook/July/5"

(4,1 and 2,2 transformation)
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4.1 clone 6 extracted DNA (which presented a good size strip on electrophoresis)
 
4.1 clone 6 extracted DNA (which presented a good size strip on electrophoresis)
  
6 clones of each of the other transformations pPS16_001, pPS16_002, pPS16_003, pPS16_005 and pPS16_006 were placed on culture in 4mL of LB added to Ampicillin (50
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6 clones of each of the other transformations pPS16_001, pPS16_002, pPS16_003, pPS16_005 and pPS16_006 were placed in 4mL of LB added to Ampicillin (50µg/mL) at 37°C, 180RPM.  For 2.2 just 2 clones were cultivated because there was not more colony.
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Revision as of 13:32, 12 July 2016

Tuesday 5th July

Lab work

Visualization

Transformation of DH5α|pPS16_004 and DH5α|pPS16_007

The 04/06/2016 transformations show white colony growth for G-blocks 4.2 clone 3 and GFP1-9 (clone 1), but blue colonies only for 4.1 clone 3.

Thus this last G-block 4.1 clone 3 was transformed again following the same protocol as the 21/06/2016 with : 50μg of competent DH5α cells 4.1 ligation product in 5μL of the plasmid puc19 4.1 clone 6 extracted DNA (which presented a good size strip on electrophoresis)

6 clones of each of the other transformations pPS16_001, pPS16_002, pPS16_003, pPS16_005 and pPS16_006 were placed in 4mL of LB added to Ampicillin (50µg/mL) at 37°C, 180RPM. For 2.2 just 2 clones were cultivated because there was not more colony.