Source: Contributed by Nanci Donacki Abstract: Provides detailed protocol for establishing a working cell bank Date Added: 2002-05-14 Date Modified: 2004-04-27 Purpose To describe the preparation of a Working Cell Bank Safety See SP 09-001 for lab safety considerations for the cell culture lab. Equipment -
Laminar Flow Hood -
Freezers, -70oC or Rate-Controlled Freezer -
Liquid Nitrogen Freezer Materials -
Cryovials, 1.8 ml (Nunc or equivalent) -
Cryovial rack (Nunc or equivalent) -
Sterile Centrifuge tubes, 50 ml (VWR # 21008-146 or equivalent) -
Fetal Bovine Serum, heat inactivated (BioWhittaker # 14-503F or equivalent) -
Sterile DMSO (Sigma # D2650 or equivalent) -
Sterile Pipets of appropriate sizes -
Ice -
Permanent Marking Pen -
Lab Coat -
Latex Gloves -
70 % alcohol or equivalent -
Trypan Blue, 0.4% (GIBCO # 630-5250AG or equivalent) -
Hemocytometer -
Nunc Freezing Container (# 5100-0001) -
Freezer Log Procedure -
The Master Cell Bank must be tested for sterility and viability before the Working Cell Bank is prepared/ -
The Working Cell Bank consists of 50 vials of cells at 5 x 106 cells/vial. -
The day before freezing, refeed the cells with fresh medium, or add additional medium to suspension cultures to ensure that they are in log phase of growth. -
Chill the Freezing medium on ice. -
Label with cryotubes with the cell line name, the cells/vial, and the date. Include on the label that the vials are the Working Cell Bank. Place the vials in the cryotube rack and place the rack on ice. -
Prepare a single cell suspension, use trypsin for adherent cell line. -
Take an aliquot for a cell count. Count the cells using a hemocytometer, according to the current revision of SP 05-009. Determine the viability using trypan blue stain, according to the current revision of SP 09-005. NOTE: The cells must have greater than 90% viability before proceeding. If the cells are less than 90% viability, do not freeze. -
Transfer the cell suspension to centrifuge tubes. -
Centrifuge at 1000 rpm for 5 minutes, 2-8oC. -
Siphon off all the medium. -
Slowly add chilled freezing medium to yield 5 x 106 cells/ml. Resuspend the cells in the freezing medium by gently pipetting. -
Place the tube on ice. Dispense the cells, 1 ml/vial, into the labeled cryovials. Recap vials tightly. Complete all vials. -
Place the vials into the Nunc Freezing Container. Replace the lid. -
Place the Freezing Container in the -700C Freezer overnight. -
Transfer the vials to the vapor phase of the liquid nitrogen freezer. -
Record the cell line information and location in the Freezer Log. Protocol Online
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