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1 Department of Biological
Sciences, Kent State University, Kent, Ohio
A technique is described for the rapid isolation
of principal cells from enzymatically dispersed
rat caput epididymidis by differential sedimentation into calf serum. Sedimentations
were prepared in common glass separatory
funnels. Sperm-free, principal cell populations
that were 66.6% pure and averaged 106 cells
were isolated after 10 minutes of sedimentation.
This represents a twofold enrichment in principal cells over that achieved in the dispersed
tissue suspension. Based on dye exclusion
tests, viability of principal cells after separation
was 90%, suggesting that the cells are well
suited for physiologic study.
Key words: epididymis, principal cell, rapid isolation
Submitted on February 25, 1980
Revised on December 1, 1980
Accepted on February 26, 1981
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