| Cryopreservation of cells | ||||
| 1. Allow the cells to attain 70% confluence 2. Repeat the steps from 1-8 3. Discard the supernatent and suspend pellet in 2ml of cryomedium using a sterile pipette. 4. Transfer it to a cryovial and label it appropriately 5. Leave the vial in the freezer (4'C for 1 hour) and transfer it to -20'C for 24 hours and finally to liquid nitrogen. |
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