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Our normal procedure for stopping carry over is to run 10% sodium
hypochlorite between samples. This removals the fluorescence from
everything we've tried - but it doesn't work with TransFlouSpheres.
I'm analysing on an Elite, an XL and a Facscan.
Any suggestions as to how to stop these beads fluorescing.
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Graham Vesey
Australian Environmental Flow Cytometry Group
School of Biological Sciences, .-.--:_:\
Macquarie University, _/ \
Sydney, : AEFCG |
Australia NSW 2109. \_ /
Tel- 612 850 8150 '-''''\__/
Fax- 612 850 8174 V
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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;
Web