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 11th July 1.1 Lab work 1.1.1 Biobrick characterization 1.1.1.1 Electrocompetents and transformation by electroporation of BL21 1.1.2 Bringing DNA closer 1.1.2.1 DH5α transformation with ST1, NM, SP and TD Monday 11th July Lab work Biobrick characterization Electrocompetents and transformation by electroporation of BL21 By Charlène BL21 cells were grown up to OD600nm=7.14. They were then made competent and transformed with K1372001 extracted from clone 2 and pcl_TAA, pcl_TAG or pcl_Tq to create the following strains: BL21|K1372001+pcl_TAA BL21|K1372001+pcl_TAG BL21|K1372001+pcl_Tq Bringing DNA closer DH5α transformation with ST1, NM, SP and TD By Laetitia and Mathilde DS-NMcas, DS-SPcasN-, DS-ST1cas-N and DS-TDcasN- plasmids were resuspended with 5μL of sterilized water. 5 tubes were prepared : one control tube with only 50μL of DH5α heat-shock competent cells four tubes with 50μL of DH5α heat-shock competent cells + 1μL of plasmid The regular heat-shock competent cells transformation protocol was used. Petri dishes preparation : 200mL of LB Agar 130μL (50μL/mL) of spectinomycin Transformed cells were plated in duplicata (10μL and 50μL) on 8 plates. Control cells were plated on another plate.
By Charlène
BL21 cells were grown up to OD600nm=7.14. They were then made competent and transformed with K1372001 extracted from clone 2 and pcl_TAA, pcl_TAG or pcl_Tq to create the following strains:
By Laetitia and Mathilde
DS-NMcas, DS-SPcasN-, DS-ST1cas-N and DS-TDcasN- plasmids were resuspended with 5μL of sterilized water. 5 tubes were prepared :
The regular heat-shock competent cells transformation protocol was used.
Petri dishes preparation :
Transformed cells were plated in duplicata (10μL and 50μL) on 8 plates. Control cells were plated on another plate.
