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 1.1.1.2 Sequencing of 1.2, FKBP, FRB 1.1.1.3 Purification on gel of gBlocks 3 and 4 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 IPS83 and IPS84 0,13µL of Dream Taq Polymerase 19,37 µL of H20 Colonies were put into sterile water, put through 5 minutes of denaturation before the addition of the mix. Annealing temperature was 57°c. After amplification, 1µL of each PCR product and 10µL of the DNA purple ladder were palced in wells and migrated at 100V for 30min. Sequencing of 1.2, FKBP, FRB Terrence and Léa Was sent : Clone Concentration size 1.2 11 392.66 3934 FKBP 3 272.37 3393 FKBP 4 404.65 3393 FKBP 5 204.87 3393 FRB 2 256.44 3347 FRB 5 129.86 3347 Purification on gel of gBlocks 3 and 4 Terrence and Mathilde After amplification, 50µL of each PCR product diluted 6 tumes with 10 µL of the gel loadding dye, and 10µL of the DNA purple ladder were placed in wells and migrated at 100V for 30min. The extraction was carried out with the usual protocol.
By Mathilde
Clones 7,8,9 and 10 of pPS16_016 were amplified following the protocol :
Colonies were put into sterile water, put through 5 minutes of denaturation before the addition of the mix. Annealing temperature was 57°c. After amplification, 1µL of each PCR product and 10µL of the DNA purple ladder were palced in wells and migrated at 100V for 30min.
Terrence and Léa
Was sent :
Terrence and Mathilde
After amplification, 50µL of each PCR product diluted 6 tumes with 10 µL of the gel loadding dye, and 10µL of the DNA purple ladder were placed in wells and migrated at 100V for 30min. The extraction was carried out with the usual protocol.
