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 Friday 22nd July 1.1 Lab work 1.1.1 Biobrick characterization 1.1.1.1 Low Fidelity Dreamtaq PCR of transformed DH5α with pPS16_002 1.1.1.2 High Fidelity Q5 PCR of transformed DH5α with pPS16_004 and pPS16_007 Friday 22nd July Lab work Biobrick characterization Low Fidelity Dreamtaq PCR of transformed DH5α with pPS16_002 By Mathilde A DreamTaq PCR was made with transformed cultures pPS16_002 following the usual protocol with Tm at 57°c and 5min for the initial denaturation. We divided up the PCR mix in 6 PCR tubes and added in each one a different clone from the transformed culture. The picked colonies were re-plated on a petri dish medium LB + Ampicillin (50µg/mL) + xGal/IPTG (1/1000). Results : PCR products expected were : Plasmid pPS16_002 Bande Size pb 960 The electropheresis on agarose gel showed absolutely no PCR products. From this day, transformed culture from the 22/07/2016 will be used for the PCR experiments instead of those from the 19/07/2016. High Fidelity Q5 PCR of transformed DH5α with pPS16_004 and pPS16_007 By Laetitia The PCR was performed following the usual protocol. 8 tubes were done: 5 clones of pPS16_004 and 3 clones of pPS16_007 The TM was at 60°C
By Mathilde
A DreamTaq PCR was made with transformed cultures pPS16_002 following the usual protocol with Tm at 57°c and 5min for the initial denaturation.
We divided up the PCR mix in 6 PCR tubes and added in each one a different clone from the transformed culture. The picked colonies were re-plated on a petri dish medium LB + Ampicillin (50µg/mL) + xGal/IPTG (1/1000).
Results : PCR products expected were :
The electropheresis on agarose gel showed absolutely no PCR products. From this day, transformed culture from the 22/07/2016 will be used for the PCR experiments instead of those from the 19/07/2016.
By Laetitia
The PCR was performed following the usual protocol. 8 tubes were done: 5 clones of pPS16_004 and 3 clones of pPS16_007
The TM was at 60°C
