[Histonet] What is the best way to decontaminate a cryostat?
We have an old cryostat (without UV) with which we wish to produce sections
for subsequent laser capture micro-dissection - to extract RNA for our
functional genomics projects.
Naturally we need to keep the level of cross contamination between specimens
to an absolute minimum.
Could anyone tell me the best way to decontaminate a cryostat for this
purpose (what you use and how you do it).
Many thanks for your help.
Dr. Peter Bannister,
Thrombosis Research Institute,
Emmanuel Kaye Building,
London SW3 6LR.
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