[Histonet] Formalin fix---then freeze?
KMIN (Kathy Mink)
minkk <@t> zgi.com
Tue Jul 13 11:35:26 CDT 2004
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 <@t> umdnj.edu]
Sent: Tuesday, July 13, 2004 10:31 AM
To: KMIN (Kathy Mink)
Cc: histonet <@t> 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
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voice: (732)-235-4583; fax: -4029
mcauliff <@t> umdnj.edu
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