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Updated: May 24, 2026

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Freezing Human ES Cells
Published on: October 12, 2006
A simple freezing medium for serum-free cultured cells
1GENE BANK, The Institute of Physical and Chemical Research, (RIKEN), 3-1-1 Koyadai, 305, Tsukuba-shi, Japan.
Cytotechnology
|February 24, 2012
Summary
Methylcellulose protects serum-free cultured cells during freezing and thawing. A new simple freezing medium containing methylcellulose and dimethylsulfoxide is effective for cell cryopreservation.
Area of Science:
- Cell biology
- Cryopreservation techniques
- Biotechnology
Background:
- Serum-free cell culture is crucial for reducing variability and simplifying downstream processing.
- Cryopreservation is essential for long-term storage and transport of cell lines.
- Protecting cells from freeze-thaw damage is a significant challenge in cell culture.
Purpose of the Study:
- To evaluate the protective effect of methylcellulose on serum-free cultured cells during cryopreservation.
- To formulate a simple and effective freezing medium for serum-free cell culture.
Main Methods:
- Cells cultured in serum-free medium were frozen using a newly formulated medium.
- The formulated medium contains methylcellulose (0.1%), dimethylsulfoxide (10%), and a base serum-free culture medium (e.g., MEM).
- Cell viability and recovery after freeze-thaw cycles were assessed.
Main Results:
- Methylcellulose demonstrated a protective effect against the detrimental impacts of freezing and thawing on serum-free cultured cells.
- The formulated medium, comprising 0.1% methylcellulose, 10% dimethylsulfoxide, and a standard serum-free medium, proved suitable for freezing these cells.
- High cell viability was observed post-thaw when using the methylcellulose-based freezing medium.
Conclusions:
- Methylcellulose is an effective cryoprotective agent for serum-free cultured cells.
- A simple, methylcellulose-based freezing medium can be readily prepared for preserving serum-free cell cultures.
- This formulation offers a practical solution for maintaining the integrity of cells in serum-free conditions during cryopreservation.

