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 21th July 1.1 Lab work 1.1.1 Biobrick characterization 1.1.1.1 K1372001 from clone 2 digestion 1.1.2 Visualization 1.1.2.1 1.1.3 Get DNA Closer 1.1.3.1 Thursday 21th July Lab work Biobrick characterization K1372001 from clone 2 digestion By Alice and Terrence We made a digestion of K1372001 plasmid following this protocol. We used EcoR1 and Pst1 fast digest enzymes. After incubation, 3.3 mL of loading dye is added to digestion products. We put in wells 10µL of DNA ladder and 20 µL of digestion products. We set the eletrophoresis machine at 100V for 25min. Digestion products expected were : Band size (Bp) Plasmid 1590 Insert 2029 Visualization By Get DNA Closer By
By Alice and Terrence
We made a digestion of K1372001 plasmid following this protocol. We used EcoR1 and Pst1 fast digest enzymes. After incubation, 3.3 mL of loading dye is added to digestion products. We put in wells 10µL of DNA ladder and 20 µL of digestion products. We set the eletrophoresis machine at 100V for 25min.
Digestion products expected were :
By
