Team:TU Darmstadt/Protocols/Metabolism
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<span style="font-size:200%;"><span style="color:#00689D;">Protocols Metabolism</span></span> | <span style="font-size:200%;"><span style="color:#00689D;">Protocols Metabolism</span></span> | ||
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The following page give an overview of the standard protocols used by the team Metabolism in iGEM PET.erminators project 2012. | The following page give an overview of the standard protocols used by the team Metabolism in iGEM PET.erminators project 2012. | ||
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+ | = Protocols Metabolism = | ||
== In vivo == | == In vivo == |
Revision as of 14:23, 9 September 2012
Protocols Metabolism
The following page give an overview of the standard protocols used by the team Metabolism in iGEM PET.erminators project 2012.
Contents |
Protocols Metabolism
In vivo
Production of chemically competent cells
Production of chemically competent cells
- Inoculate 10 ml of LB-Media with an E. coli colony and incubate at 37 °C overnight
- Inoculate 200 ml of LB-Media with 2.5 ml of the overnight culture
- Incubate the culture at 37 °C until an OD600 of 0.5
- Cool the cells on ice for 5 min
- Centrifuge the cells for 10 min at 5000 rpm and 4 °C
- Resuspend the cell-pellet in 32 ml pre-cooled CaCl2 solution (Do not vortex!)
- Add pre-cooled CaCl2 solution to 200 ml
- Let the cells repose on ice for 1 hour
- Centrifuge the cells for 10 min at 5000 rpm and 4 °C
- Resuspend the pellet in 10 ml cryo-solution
- Decant 200 µl of competent cells in a 1.5 ml tube
- Store the tube in an -80 °C freezer
Solutions
- CaCl2
- 5.55 g CaCl2
- Add di H2O to 1 L
- Sterilize by autoclaving
- Cryo solution
- 0.278 g CaCl2
- 10 ml glycerin
- Add di H2O to 50 ml
- Sterilize by autoclave