David

That does work, we have done it here on mouse muscle and liver,  but there are 
some problems to fixed and then frozen tissue.  The tissue  on occasion does 
not stay on the slide as well once it sectioned, even with plus slides.  

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
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-----Original Message-----
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of David Burk
Sent: Thursday, March 20, 2014 9:55 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Oil Red O staining question

Experts!

 

Is there any reason you would not consider formalin fixation followed by 
cryoprotection/cryosectioning for Oil Red O (or bodipy for that matter) 
staining of mouse muscle? 

I ask as many folks seem to have difficulty in the flash freezing aspect of 
tissue collection and end up with lots of ice crystal damage. While the above 
method is still subject to freezing artifact it does at least negate the 
'rushed collection' part of the process.

 

The literature favors flash frozen tissue but we've done successful staining of 
liver that has been fixed then cryoprotected prior to staining and things 
looked fine. Is there an issue with tissue adhering to slides after sectioning 
or some other reason this method is not preferred?

 

I value your opinion as I am wondering why one would choose one approach over 
the other.  Let's pretend tissue antigenicity isn't a factor - only section 
quality and lipid droplet staining.

 

Thanks for your comments!

 

David

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