Team:TU Darmstadt/Protocols/Chemically competent cells
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== Chemically competent cells == | == Chemically competent cells == | ||
- | The [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Bacterial_transformation transformation | + | The [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Bacterial_transformation transformation] of ''E. coli'' with plasmid DNA via [https://2012.igem.org/Team:TU_Darmstadt/Protocols/Heat_Shock_Transformation heatshock transformation] requires chemically competent cells. |
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== Materials == | == Materials == | ||
=== Equipment === | === Equipment === |
Revision as of 16:35, 16 September 2012
Contents |
Chemically competent cells
The transformation of E. coli with plasmid DNA via heatshock transformation requires chemically competent cells.
Materials
Equipment
- -80°C freezer
- Incubation shaker
- Centrifuge (cooling cababilities required!)
- photometer
- Ice water bath
Chemicals & consumables
- Ice and/or liquid nitrogen
- Falcon tubes
- dYT Medium (50 ml p.c.)
- ice cold 100mM CaCl2
Procedure
- 2mL preculture E.coli in DYT-medium
- incubate preculture overnight at 37°c
- inoculate 200 mL with the preculture
- incubate at 37°C and 150 rpm till an OD600 of 0.4 - 0.6 is reached
- incubate cells on ice for 15 min
- centrifuge the culture at 4°C and 3000 x g for 10 min (the following steps are done on ice)
- resuspend cell pellet in 10mL ice cold 100 mM CaCl2
- incubate on ice for 1 hour
- centrifuge the culture at 4°C and 3000 x g for 10 min
- resuspend cell pellet in 10mL ice cold 100 mM CaCl2
- incubate on ice for 1 hour
- centrifuge the culture at 4°C and 3000 x g for 5 min
- resuspend cell pellet in 2mL ice cold 100 mM CaCl2 and 15 % (v/v) glycerine
- incubate on ice for 30 min
- aliquot the cells à 100µL
- store at -80°C
References
- Mandel, M. and Higa, A.: Calcium-dependent bacteriophage DNA infection. J Mol Biol, 1970, 53, 159-162