Answers are grounded in this paper and cite their sources.
Mouse fibroblasts of strain L (Earle) and human epithelial cells of strain HeLa (Gey) have been preserved successfully at −60° to −70°C for 6 and 7 months, respectively. Glycerol in the suspending liquid greatly increased the percentage of surviving cells. Solutions of glycerol (5% for strain L and 20% or 30% for strain HeLa) in a solution for maintenance of animal cells (MS), in balanced salt solution, or in serum (horse serum for strain L cells, adult human serum for strain HeLa cells), were of approximately equal value for the periods of preservation studied. The cells survived storage poorly at −60° to −70°C when suspended in undiluted serum or in 5% dextrose in water. Strain L cells were preserved in slightly greater numbers after freezing over a period of 1–1.5 hours than after freezing in 3-5 minutes; strain HeLa cells survived both freezing procedures equally well. Better preservation of both cell types resulted from storage at −60° to −70°C than at −20°C, and from thawing in 1–2 min. rather than in 30–60 minutes. The value of low temperature preservation for handling and maintenance of strain L and strain HeLa cells and for preservation of strain stability is discussed.
No takes yet. Share an insight, caveat, or question.
Scherer et al. (1954) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: