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.

Hosted by www.Geocities.ws

1