Abstract
A simple scheme for purification of murine myeloma cells from ascites fluid without loss of viability is presented. This is accomplished by repeated differential centrifugations followed by passage through a glass bead column. The cells so obtained are 99.9 per cent pure and 99 per cent viable in a large number of repetitions of this technic.
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© 1967 by American Society of Hematology, Inc.
1967
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