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 Monday 22th August 1.1 Lab work 1.1.1 Visualization 1.1.1.1 Low fidelity Dreamn Taq PCR of pPS16_016 Monday 22th August Lab work Visualization Low fidelity Dreamn Taq PCR of pPS16_016 By Mathilde Clones 7,8,9 and 10 of pPS16_016 were amplified following the protocol : 1,5µL of Green Buffer 1µL of dNTPs 1µL of each primers 1151 and 1151 0,13µL of Dream Taq Polymerase 19,37 µL of H20 Colonies were put into sterile water, and were put trhough
By Mathilde
Clones 7,8,9 and 10 of pPS16_016 were amplified following the protocol :
Colonies were put into sterile water, and were put trhough
