Journal article
A method for freezing synchronous mitotic and G1 cells
Experimental cell research, Vol.170(2), pp.363-368
1987
DOI: 10.1016/0014-4827(87)90313-2
PMID: 3595736
Abstract
A modification of the protocol developed by Kawamoto, J C & Barrett, J N, Brain res (1986), in press [3] for freezing primary neuron cultures in a solution containing low sodium and high lactate and potassium concentrations was used to freeze synchronous mitotic and G1 CHO cells. After thawing, the cells behaved as if they had never been frozen with respect to cell growth, cell division, plating efficiency, and hyperthermic sensitivity.
Details
- Title: Subtitle
- A method for freezing synchronous mitotic and G1 cells
- Creators
- M. J BORRELLI - Univ. California, radiation oncology res. lab., San Francisco CA 94143, United StatesM. A MACKEY - Univ. California, radiation oncology res. lab., San Francisco CA 94143, United StatesW. C DEWEY - Univ. California, radiation oncology res. lab., San Francisco CA 94143, United States
- Resource Type
- Journal article
- Publication Details
- Experimental cell research, Vol.170(2), pp.363-368
- Publisher
- Elsevier; Orlando, FL
- DOI
- 10.1016/0014-4827(87)90313-2
- PMID
- 3595736
- ISSN
- 0014-4827
- eISSN
- 1090-2422
- Language
- English
- Date published
- 1987
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Radiology
- Record Identifier
- 9984064227802771
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