Team:LMU-Munich/Notebook/Protocols/7 Measurement of competence
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** This can be made by diluting 1 μl of NEB pUC19 plasmid (1 μg/μl, NEB part number N3401S) into 100 ml of TE | ** This can be made by diluting 1 μl of NEB pUC19 plasmid (1 μg/μl, NEB part number N3401S) into 100 ml of TE | ||
* Hold on ice 0.5 hours | * Hold on ice 0.5 hours | ||
- | * Heat shock 60 sec at | + | * Heat shock 60 sec at 42°C |
* Add 250 μl [[Team:LMU-Munich/Notebook/Protocols/8_SOC_medium|SOC]] | * Add 250 μl [[Team:LMU-Munich/Notebook/Protocols/8_SOC_medium|SOC]] | ||
- | * Incubate at | + | * Incubate at 37°C for 1 hour in 2 ml centrifuge tubes rotated |
** using 2ml centrifuge tubes for transformation and regrowth works well because the small volumes flow well when rotated, increasing aeration. | ** using 2ml centrifuge tubes for transformation and regrowth works well because the small volumes flow well when rotated, increasing aeration. | ||
** For our plasmids (pSB1AC3, pSB1AT3) which are chloramphenicol and tetracycline resistant, we find growing for 2 hours yields many more colonies | ** For our plasmids (pSB1AC3, pSB1AT3) which are chloramphenicol and tetracycline resistant, we find growing for 2 hours yields many more colonies |
Latest revision as of 13:21, 13 August 2010
Source:http://partsregistry.org/Help:Protocols/Competent_Cells
Measurement of competence