Table of Contents
Cell reviving process is a method of the subsequent recovery of the cryopreserved cells.
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The steps of 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) The 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°C, with 5% CO2 and humid conditions.
Other related notes:
- Cell cycle checkpoints: https://thebiologyislove.com/cell-cycle-checkpoints/
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