[Histonet] Alcohol fixation and immuno

[Lynette Pavelich]

Normally, we used regular charged slides, but we found some slides from Surgipath to help with those "hard to stay on" type tissues.  They are called "Apex", Superior Adhesive Slides.  Product # 00084.  They are frosted on one end, and come in different colors.  That product # is Pink.
They are not always 100%, but nothing is!  A challenging but wonderful field!

hope this helps,
Lynette

>>> Rene J Buesa <rjbuesa <@t> yahoo.com> 2/2/2010 1:03 PM >>>
Exactly!
Your tissue suffer (that is the appropriate word) a double fixation, probably partial in  both, but the formalin step will cross link the proteins requiring epitope retrieval.
René J.

--- On Tue, 2/2/10, Martin, Erin <Erin.Martin <@t> ucsf.edu> wrote:


From: Martin, Erin <Erin.Martin <@t> ucsf.edu>
Subject: [Histonet] Alcohol fixation and immuno
To: "histonet" <histonet <@t> lists.utsouthwestern.edu>
Date: Tuesday, February 2, 2010, 10:24 AM


Good morning everyone,
We occasionally receive specimens that were fixed in alcohol but processed on our machine, which starts in formalin.  In our typical antigen retrieval we either use a 95 degree waterbath for an hour or enzyme for 5 minutes.  On alcohol fixed tissues this chews up the tissue but we get staining.  If we repeat the stains with no retrieval to try to minimize the damage, we get very weak or no staining at all (in a general sense - I'm not speaking about any particular antibody).  Is this because we have a small degree of formalin fixation because of the formalin step on the processor?  Enough to require some retrieval but not as much as formalin fixed tissue?  Has anyone else run into this problem?  If so, how did you solve it?

Thank you for you help!
Erin Martin
UCSF Dermatopathology

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