Freezing of C2C12 cells: Difference between revisions
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==Procedure:== | ==Procedure:== | ||
* wash the cells with 5 ml PBS | |||
* remove the PBS and add 2 ml TE | |||
* let it incubate for 3 – 5 min | |||
* stop the TE with 5 ml HS – media and resuspend the cells | |||
* pipette the cell suspension back in the FALCON tube | |||
* centrifuge the cells (1000 xg, 3 min at 4 ºC) | |||
* remove the old media | |||
* resuspend the cells 1 ml freezing media | |||
* quickly pipette the liquid in the cryo tube | |||
* put the cells in the freezing box and store this for one day at –80 ºC | |||
* place the cells one day later into the liquid nitrogen |
Revision as of 07:41, 24 October 2014
Materials:
- 15 ml FALCON tube
- PBS w/o Ca2+ and Mg2+
- TE in PBS
- Freezing media (10% DMSO + 40% serum + 50% DMEM)
- Pipettes and tips
- Glas pipetts
- cryo tube
- ice
- freezing box
Procedure:
- wash the cells with 5 ml PBS
- remove the PBS and add 2 ml TE
- let it incubate for 3 – 5 min
- stop the TE with 5 ml HS – media and resuspend the cells
- pipette the cell suspension back in the FALCON tube
- centrifuge the cells (1000 xg, 3 min at 4 ºC)
- remove the old media
- resuspend the cells 1 ml freezing media
- quickly pipette the liquid in the cryo tube
- put the cells in the freezing box and store this for one day at –80 ºC
- place the cells one day later into the liquid nitrogen