Thank you all for the great response.  What would we do without the histonet?  You guys are wonderful.

Kathy Mink

-----Original Message-----
From: Geoff McAuliffe [mailto:mcauliff@umdnj.edu]
Sent: Tuesday, July 13, 2004 10:31 AM
To: KMIN (Kathy Mink)
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Formalin fix---then freeze?


Hi Kathy:

    This method is very do-able, is common and does make sense; you get 
the benefits of fixation (better morphology) and benefits of frozen 
sections (fat stains, immuno stains). I would suggest throwing in a 
cryoprotection step (20-30% sucrose overnight in the refrigerator) after 
washing out the formalin and, of course, rapid freezing to avoid ice 
crystal artifacts.

Geoff

KMIN (Kathy Mink) wrote:

>Hi,
>
>I have been asked an unusual (stupid?) question and hope someone can help.  Is it possible to formalin fix a tissue and then put it in OCT and freeze it to cut frozen sections?  I know it doesn't make much sense but apparently a contract we have was worded this way (obviously not proof read by the pathologist) and now I need to treat the tissue this way if possible.  Help!
>
>Kathy Mink
>
>
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>  
>

-- 
--
**********************************************
Geoff McAuliffe, Ph.D.
Neuroscience and Cell Biology
Robert Wood Johnson Medical School
675 Hoes Lane, Piscataway, NJ 08854
voice: (732)-235-4583; fax: -4029 
mcauliff@umdnj.edu
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