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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