[Histonet] Frozen section artefact

Adam Boanas a.boanas <@t> epistem.co.uk
Wed Sep 26 01:37:26 CDT 2012

Hi again,

In your opinion is it better to fix frozen sections prior to storage in -80 or following removal from -80 prior to a run?

-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu [mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Hobbs, Carl
Sent: 25 September 2012 18:37
To: histonet <@t> lists.utsouthwestern.edu
Subject: Re: [Histonet] Frozen section artefact

Assuming that you are fixing fresh-frozen tissue sections:

Tissue is autolysing.

Use Formalin for 10 mins or 1:1 acetone:alcohol for 10 mins.

Imho, acetone is not a fixative..it's a delipidizer.

5 mins in that mixture is too short a time for the alcohol to be an effective coagulant fixer.

However, a longer time in alcohol may well mask your Ag sites.

I see this artefact in acetone fixed frozen sections, often.

When immunostaining for MHCs in muscle, no fixation is required but, if DAPI/Hoechst is included....nuclear streaming will be seen.

Always try several fixing fluids to get the best results on any new Ab.

 I may be wrong....happy to be corrected.

Curious always,


Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu

This message has been scanned for malware by Websense. www.websense.com

More information about the Histonet mailing list