Re: IHC storage alcohol
|From:||Robert Schoonhoven <email@example.com>|
We usually store our tissues in 70% ETOH at 4oC after fixation until
they can be put on the processor. I have also had tissues shipped to me
from Europe and Canada in phosphate buffer (not PBS) after 48 hour NBF
fixation with no loss of antigenicity of cell cycle markers. I can't
really say how other antbodies would be affected.
Jan Shivers wrote:
> Usually the tissue samples I receive have been optimally fixed (time-wise)
> in formalin and promptly embedded into paraffin. Today I received a call
> from a researcher out of state who wants to send me some samples, but cannot
> get his fixed tissue processed into paraffin within a 24-hour period after
> start of fixation. He wants to know what storage alcohol he should switch
> the samples into until embedding, and I became brain-dead. Can someone help
> me out here PDQ? Is it 70% ethanol or some other percentage? Is there a
> better storage medium than ethanol? I have received some cases in PBS
> (post-formalin-fixation), but those staining results were less than optimal.
> Any help would be greatly appreciated.
> Jan Shivers
> Univ. of Minn. Vet. Diag. Lab
Laboratory of Molecular Carcinogenesis and Mutagenesis
Dept. of Environmental Sciences and Engineering
University of North Carolina
Chapel Hill, NC 27599
Don't go around saying the world owes you a living; the world owes you
nothing; it was here first.
Mark Twain [Samuel Langhornne Clemens] (1835-1910)
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