Toggle navigation Home Team Team Media Collaborations Sponsors Acknowledgements Project Background Design CRISPR/Cas9 Strategy Experiments Notebook Results Perspective Interlab Study Parts Parts Basic Parts Composite Parts Human Pratices Overview Societal Issues of CRISPR/Cas9 Responsible Research and Innovation GMO regulation Integrated Practices Engagement Model Attributions Safety Contents 1 Thursday 7th July 1.1 Lab work 1.1.1 Visualization 1.1.1.1 PCR products migation 1.1.1.2 Cultures results Thursday 7th July Lab work Visualization PCR products migation By Caroline and Léa gBlocks screened the 06/07/2016 were put on migration. The usual protocol was followed. 20µL of each PCR product was added to 4µL of purple loading dye 6X. PHOTO GEL pas dans le cahier ! Cultures results There was no blue colony observed on xGal/IPTG + ampicillin mediums for transformed transformed pPS16_004, pPS16_007 and the pPS16_007 clone 6 gBlocks.
By Caroline and Léa
gBlocks screened the 06/07/2016 were put on migration. The usual protocol was followed. 20µL of each PCR product was added to 4µL of purple loading dye 6X.
PHOTO GEL pas dans le cahier !
There was no blue colony observed on xGal/IPTG + ampicillin mediums for transformed transformed pPS16_004, pPS16_007 and the pPS16_007 clone 6 gBlocks.
