MahnaziGEM (Talk | contribs) |
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Plasmid pZA11 were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit | Plasmid pZA11 were extracted using the [[Team:Paris_Saclay/Experiments#InvitrogenPlasmidExtraction|"Charge Switch-Pro Plasmid Miniprep"]] kit | ||
+ | |||
+ | ====Gibson Assembly of segments 1 and 2==== | ||
+ | ''By Mahnaz'' | ||
+ | |||
+ | Two preparations were made : | ||
+ | * the 1-2 Gibson assembly product tube : 1,12µL of purified segment 1 and 0,56µL of purified segment 2 + 0,85µL of digested pSB1C3 + 7,47 µL of sterile water + 10µL of NEB Builder Hifi DNA Assembler Master Mix | ||
+ | * the control tube : 0,85µL of digested pSB1C3 + 17,47 µL of sterile water | ||
+ | |||
+ | Gibson products were incubated 1h at 52°c. | ||
+ | |||
+ | ====Transformation in DH5α with the 1-2 Gibson assembly product==== | ||
+ | ''By Mahnaz'' | ||
+ | |||
+ | The transformation was performed following the usual [[Team:Paris_Saclay/Experiments#Heat_shock_competent_cells|protocol]] with 2µL of plasmid. | ||
+ | * 50, 150 and 350µL of the transformed DH5α with the 1-2 Gibson assembly product were plated on 3 plates of LB + chloramphenicol (30µg/mL) | ||
+ | * 350 µL of each Gibson assembly control and transformation control were plated on 2 plates of B + chloramphenicol (30µg/mL) | ||
+ | |||
+ | Petri cultures were incubated at 37°c overnight. | ||
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} |
Revision as of 16:47, 20 September 2016