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{{Team:Paris_Saclay/notebook_header}} | {{Team:Paris_Saclay/notebook_header}} | ||
− | =Wednesday 22<sup> | + | =Wednesday 22<sup>nd</sup> June= |
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− | ==== | + | ====Heat-shock competent cells (cf. [[Team:Paris_Saclay/Experiments#HeatShockCompetent|protocol]])==== |
''By Marion'' | ''By Marion'' | ||
At 10am OD was 0.3. At 1pm OD was 0.46. At 3pm OD was 0.62. | At 10am OD was 0.3. At 1pm OD was 0.46. At 3pm OD was 0.62. | ||
− | The solution was put on ice 10min (stop the OD). After, it was centrifuged 10min at 4°C at 3000rpm. The pellet was resuspended in 80mL ice-cold TB and incubated on ice for 10min. The solution was centrifuged again at 4°C at 3000rpm. The pellet was resuspended in 20mL ice-cold TB and DMSO was added at 7% of the final concentration (1.58mL of DMSO for 21mL of TB+cells). The solution was incubated on ice for 10min and then distributed in tubes, frozen in liquid nitrogen and stored at -70°C. | + | The solution was put on ice 10min (in order to stop the OD). After, it was centrifuged 10min at 4°C at 3000rpm. The pellet was resuspended in 80mL ice-cold TB and incubated on ice for 10min. The solution was centrifuged again at 4°C at 3000rpm. The pellet was resuspended in 20mL ice-cold TB and DMSO was added at 7% of the final concentration (1.58mL of DMSO for 21mL of TB+cells). The solution was incubated on ice for 10min and then distributed in tubes, frozen in liquid nitrogen and stored at -70°C. |
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===Interlab study=== | ===Interlab study=== | ||
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''By Lea and Caroline'' | ''By Lea and Caroline'' | ||
− | No colony grew on the Petri dish. Transformations have to be | + | No colony grew on the Petri dish. Transformations have to be done again. |
− | + | The [[Team:Paris_Saclay/Experiments#ElectroCompetent|usual protocol]] was followed but this time 2µL of plasmids were taken, a new solution of antibiotic Cm was used and a positive control was added (a pSB1C3 plasmid). | |
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} |
Latest revision as of 13:05, 9 October 2016