Marek: Freeze-down/Thaw

Overview

This short protocol describes how to freeze down and thaw (or bring up) mammalian cells (e.g. HeLa, KEK293, CHO, Jurkat T cells).

Materials

List reagents, supplies and equipment necessary to perform the protocol here.

• 10-50 ml centrifuge tube
• cryo tubes
• DMSO, Tissue culture (TC)-tested (e.g. Sigma, D2650)
• Cell culture medium (depends on cell line/cells)
• Trypsin-EDTA (e.g. from PAA, L11-004) - for adeherent cells
• Freeze-down medium
  • 6% DMSO (some people prefer 10%)
  • Cell culture medium (you can use 100% fetal calf serum (FCS) instead of cell culture medium)
• Basic TC centriguge (0 - 2500 rpm)
• Freeze-down box (this could be simply made from a small styropore box and cotton or from two styropore racks from 15-ml centrifuge tubes )

Freeze-down (suspension cells)

1. Centrifuge at 1000-1200 rpm for 4-5 min at RT.
2. Suck out the medium.
3. Resuspend cells in appropriate volume of freezing medium (e.g. 1.5 ml for 1.8ml Cryo-tube).
4. Transfer cells into freeze-down box and place at -80 gr.C.

*Leave over-night at -80 gr.C.
*You can store cells at -80 gr.C for 6-12 months.
*Transfer cells into liquid nitrogen a day later for longer storage (1-20 years or so).

Freeze-down (adherent cells)

1. Wash cells with PBS.
2. Add thin layer of Trypsin-EDTA on cells (approx. 1ml for 90 mm Petri dish)
3. Observe cells under microscope until these are rounded.
4. Add serum-containing medium and resuspend cells. Transfer into centrifuge tubes.
5. Centrifuge at 1000-1200 rpm for 4-5 min at RT.
6. Suck out the medium.
7. Resuspend cells in appropriate volume of freezing medium (e.g. 1.5 ml for 1.8ml Cryo-tube).
8. Transfer cells into freeze-down box and place at -80 gr.C. (Comments as for suspension cells).

Notes

1. List troubleshooting tips here.
2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
3. Anecdotal observations that might be of use to others can also be posted here.

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