The Basic steps of the cell-reviving process 1) Cryopreserved Cells [with DMSO (Dimethyl sulfoxide)] were collected from the -80°C. 2) Then the cells were thawed rapidly in the water bath at 37 °C for 30-45 sec to protect the cells from DMSO. 3) The cells were transferred into a 15 ml falcon which already contains 6 ml of media [DMEM (Dulbecco’s Modified Eagle Medium) + 10% FBS (Foetal Bovine Serum) + 1X penicillin-streptomycin solution]. 4) The centrifugation was performed at 1100 rpm for 5 minutes. 5) The Supernatant was discarded in the beaker containing a small amount of bleach and water. The pellet was collected. 6) T he pellet was washed with media to remove the trace of DMSO. 7) The cells are resuspended in 1 ml of media. 8) The cells were transferred to the T-25 flask which already contains 4 ml of media. 9) Finally, the cells were observed under the microscope and kept in the incubator at 37°...
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