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Do you currently find the sensitivity of your flow cytometer limiting? Are
there flow cytometric techniques that should but don't work for microbes? Does
the future lie in better instrumentation or in better dyes? Please remember to
include in any correspondence the make and model of flow cytometer that you
use.
If you would like to offer your opinions then you can Email me on:
hlr@aber.ac.uk
or if you prefer you can fill in the feedback form on my website:
http://pcfcfh.dbs.aber.ac.uk/
If anyone else expresses an interest in this information then I will Email a
summary to the list or to interested individuals. If you want your views to
remain anonymous please let me know.
Of course any very recent (1995) (p)reprints in this field that you think we
should include would also be most welcome.
Snail address:
Dr Hazel M. Davey,
Institute of Biological Sciences,
Edward Llwyd Building,
University of Wales,
Aberystwyth,
SY23 3DA
WALES, U.K.
Many thanks in advance for your help,
Hazel
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| Dr. Hazel Davey (hlr@aber.ac.uk), Univ. Wales, Aberystwyth, UK, SY23 3DA |
| WWW : Flow Cytometry | Welsh | Brewing : http://144.124.112.37/index.htm |
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