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I must admit we just sort cells in a sterile fashion as we would for
culture experiments, provided the cells remain intact there is not a
big problem. There again if we extract RNA from cultured cells we
don't do RNAse-free cultures, and we certainly don't have any
RNAse-free people for fresh isolates. The main thing seems to be to
wash the cells well and make sure the RNAse protection in the lysis
buffer is adequate.
Have fun
Mike
...........................................................
Mike Salmon
Department of Rheumatology
The Medical School
University of Birmingham
Birmingham B15 2TT
United Kingdom
Tel: 44 (0)121 414 6780
Fax: 44 (0)121 414 6794
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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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