The storage of cells from different tumor lines in a mechanical freezer at -80 degrees C. Comparison to cryopreservation in liquid nitrogen.
Mariusz Z. Ratajczak, David A. Kregenow, Wojciech Kuczyński, Janina Ratajczak, Alan M. Gewirtz
Abstract
Mariusz Z. Ratajczak, David A. Kregenow, Wojciech Kuczyński, Janina Ratajczak, Alan M. Gewirtz
Abstract
This paper demonstrates that it is possible to store cells from different tumor lineages in a mechanical freezer at -80 degrees C. Tumor cells cryopreserved without controlled-rate freezing in medium containing 10% dimethyl sulfoxide (DMSO) and 10% Bovine Calf Serum (BCS) for 6 months displayed similar post-thawing viability as cells cryopreserved in liquid nitrogen at -196 degrees C. We recommend this method of cryopreservation as a convenient and less expensive alternative to liquid nitrogen storage. Further studies concerning the maximum storage time at -80 degrees C and studies comparing the optimal composition of the storage medium will further define the limitations and potential of this method.
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This paper demonstrates that it is possible to store cells from different tumor lineages in a mechanical freezer at -80 degrees C. Tumor cells cryopreserved without controlled-rate freezing in medium containing 10% dimethyl sulfoxide (DMSO) and 10% Bovine Calf Serum (BCS) for 6 months displayed similar post-thawing viability as cells cryopreserved in liquid nitrogen at -196 degrees C. We recommend this method of cryopreservation as a convenient and less expensive alternative to liquid nitrogen storage. Further studies concerning the maximum storage time at -80 degrees C and studies comparing the optimal composition of the storage medium will further define the limitations and potential of this method.
Key concepts: Cryopreservation, Liquid nitrogen, Dimethyl sulfoxide, Nitrogen, Chemistry, Andrology, Biology, Cell biology