[Histonet] Formalin fixation of cells for
paraffinembedding?
Joanne Mauger
MAUGER <@t> email.chop.edu
Fri May 21 09:10:58 CDT 2004
Marsha,
I'm not sure about thyroglobulin, but I know S-100 positivety diminishes or disappears after alcohol fixation. If its well fixed in NBF first, the following alcs don't seem to hurt.
Jo
>>> "Marsha Linville" <marshal <@t> dcla.com> 05/21/04 09:52AM >>>
Joanne,
Would one of the antigens that you speak of that doesn't like alcohol
fixation be Thyroglobulin?
Marsha Linville
DCL Medical Laboratory
Indianapolis, IN 46268
(317) 874-1232
-----Original Message-----
From: Joanne Mauger [mailto:MAUGER <@t> email.chop.edu]
Sent: Friday, May 21, 2004 6:52 AM
To: eca9 <@t> georgetown.edu; histonet <@t> lists.utsouthwestern.edu
Cc: histonet <@t> lists.utsouthwestern.edu
Subject: Re: [Histonet] Formalin fixation of cells for paraffin
embedding?
To Eva,
Wrap the pellet in lens paper,and put it in a cassette to fix and process
with your tissues. I would skip the alcohol fixation and spin the cells down
in NBF, then proceed with processing and embed as usual. Some antigens don't
like alcohol fix.
Jo
>>> "Eva C. Andersson" <eca9 <@t> georgetown.edu> 05/20/04 03:18PM >>>
Hi everyone,
My lab wants to paraffin embed some cells to be used as positive
controls for immunohisochemistry staining.
We have a cell line growing but need a good protocol for fixing the
cells with formalin. Once the cells have been fixed the pellet will be
embedded in paraffin by our histopathology department.
Does anyone have a good and easy method for the fixation part?
We will deliver the pellet to the histopathology department in 70% ethanol.
Thanks in advance,
Eva Andersson
Research Assistant
Georgetown University
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