[Histonet] AO-860 Sliding Microtome + OCT Embedded
Caroline Bass
cebass <@t> buffalo.edu
Sat Sep 24 12:29:31 CDT 2011
I've tried something very similar with fresh brain tissue. I snap froze the tissue and then mounted it on the dry ice stage with little problems. But when I cut the tissue it thawed instantly on the knife and turned into a mess, even the thicker sections. You need to maintain the sections at a cold temperature outside the block as well, so a freezer room could help.
Of course this technique works perfectly with formalin fixed sections.
> Message: 5
> Date: Fri, 23 Sep 2011 15:35:36 -0400
> From: Francis OBrien <francisobrien2007 <@t> gmail.com>
> Subject: Re: [Histonet] AO-860 Sliding Microtome + OCT Embedded
> Tissue?
> To: Rene J Buesa <rjbuesa <@t> yahoo.com>,
> histonet <@t> lists.utsouthwestern.edu
> Message-ID:
> <CAKmFSPfJPkRpO-yxPOwgrZg=5MrhHO5GN5hc2gNmKBpXvdc3gA <@t> mail.gmail.com>
> Content-Type: text/plain; charset=ISO-8859-1
>
> I would be using the freezing stage with dry ice.
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