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 Wednesday 24th August 1.1 Lab work 1.1.1 Visualization 1.1.1.1 Gel Electrophoresis of Gibson (fragment 3 + fragment 4) and GFP in PSB1C3 1.1.1.2 pPS16_002 (1.2) clones 8 and 14 and pPS16_014(SgRna Nm) clone 12 Extraction 1.1.1.3 Transformation of pPS16_010 (FRB) in pJET and pPS16_014 (SgRnaNm) in pJET Wednesday 24th August Lab work Visualization Gel Electrophoresis of Gibson (fragment 3 + fragment 4) and GFP in PSB1C3 By Terrence Clone 6 and 8 seems correct for the Gibson. Clone 2-4-7-11 are correct. pPS16_002 (1.2) clones 8 and 14 and pPS16_014(SgRna Nm) clone 12 Extraction By Terrence The extraction was carried out following the usual protocol. Result of the extraction Nano drop : size (ng/µL) 260/230 260/280 1.2.14 47.81 1.64 1.84 1.2.8 834.5 2.40 1.99 SgRna Nm 12 124.21 2.00 1.89 Transformation of pPS16_010 (FRB) in pJET and pPS16_014 (SgRnaNm) in pJET By Terrence First we made a ligation with Component Volume (µL) Reaction Buffer 10 PCR Product (FRB or Nm) 1 pJET1.2/blunt 1 water, nuclease free 7 T4 DNA Ligase 1 Then we transformed 2µL of ligation product into 50 µL of competent cells, following the usual protocol.
By Terrence
The extraction was carried out following the usual protocol.
Nano drop :
First we made a ligation with
Then we transformed 2µL of ligation product into 50 µL of competent cells, following the usual protocol.
