We use Dissect-Aide seems to work really well especially with lymph
nodes too.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of White,
Lisa M.
Sent: Thursday, June 20, 2013 1:23 PM
To:
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lee Peggy Wenk
Sent: Friday, June 21, 2013 3:19 PM
To: White, Lisa M.; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Fatty Fixation
What exactly is wrong with the fatty specimens?
If the nuclei look smudgy
What exactly is wrong with the fatty specimens?
If the nuclei look smudgy, with no nuclear detail, then it has not been
fixed long enough.
If the fat is still in the tissue and you cannot section it on a microtome,
then the tissue has not had enough time during processing, especially length
The answer is time, time, time (36h)
René J.
From: White, Lisa M. lisa.whi...@va.gov
To: histonet@lists.utsouthwestern.edu
Sent: Thursday, June 20, 2013 2:23 PM
Subject: [Histonet] Fatty Fixation
Does anyone have a method they will share to fix fatty specimens? Does
anyone utilize a stir
; histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Inviato: Giovedì 20 Giugno 2013 22:38
Oggetto: Re: [Histonet] Fatty Fixation
The answer is time, time, time (36h)
René J.
From: White, Lisa M. lisa.whi...@va.gov
To: histonet@lists.utsouthwestern.edu
Sent: Thursday, June 20, 2013 2
