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It would have to be quantitative.
There is lysis of dead cells by protease. Does that safely preserve all
viable cells ? If yes, what are the best conditions ?
I was told it can be done by density gradient, but I cannot figure out how
that should work.
Many thanks for your opinions.
Ralph M. Bohmer
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CD-ROM Vol 3 was produced by Monica M. Shively and other staff at the
Purdue University Cytometry Laboratories and distributed free of charge
as an educational service to the cytometry community.
If you have any comments please direct them to
Dr. J. Paul Robinson, Professor & Director,
PUCL, Purdue University, West Lafayette, IN 47907.
Phone: (765)-494-0757;
FAX(765) 494-0517;
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