[Histonet] RE: Tissue fixation help
C.M. van der Loos
c.m.vanderloos <@t> amc.uva.nl
Mon Oct 3 01:43:19 CDT 2005
Angela,
Long time ago we thawed a frozen tissue sample directly in (room
temp.) NBF (24-48 hs). Morphology was kept surprisingly well. Sorry,
at that time phosphorylated antibodies were not even existant....
Chris van der Loos, PhD
Dept. of Pathology
Academic Medical Center M2-230
Meibergdreef 9
NL-1105 AZ Amsterdam
The Netherlands
phone: +31 20 5665631
Date: Fri, 30 Sep 2005 08:25:24 -0400
From: Angela McNabola <angela.mcnabola.b <@t> bayer.com>
Subject: [Histonet] Tissue fixation help
To: [1]Histonet <@t> lists.utsouthwestern.edu
Good Morning,
Does anybody on the histonet have any experience with taking tissue
that has
been snap frozen in minus 80, and then "thawed" out and formalin fixed
and
paraffin embedded?
I won't get into the reasons why we have to do this, but does anyone
have a
protocol (or just slowly thaw it out and fix it??). How did your IHC
turn out,
especially when using phosphorlyated antibodies? Did you get good
morphology of
your tissue?
thanks in advance!
Angela
Angela McNabola, MS HT(ASCP)SLS, QIHC
Bayer Healthcare
400 Morgan Lane
West Haven, CT 06516
203-812-5001
angela.mcnabola.b <@t> bayer.com
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