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You need the advice of an experienced technician. Probably you will be advised
to remove the paper after fixation and before trying to obtain either paraffin
or cryostat sections. You have a histology department that processes your
fixed tissues. Ask their technicians for advice.
Another w
Hi,
I've been trying to do hair follicle analysis in mouse skin sections for
the past couple of months.I usually fix the skin in Neutral Buffer
Formaline (NBF) for 24-48 hours and then send it to our histology
department to be embedded in paraffin blocks. However,i'm repeatedly
getting cross secti
Wrong all most complete recovery can be made with phenol 95 and water over 24
hours
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-Original Message-
From: Rene J Buesa
Date: Tue, 15 Nov 2011 21:14:20
To: ;
Subject: Re: [Histonet] is there a way to recover ruined tissues
Realy recovered? No
We recently purchased Cell Marque's Glut-1 antibody and it is not staining
correctly for us. Does anyone have a working protocol for the Benchmark Ultra?
Or is the antibody from another company work anyone?
Sandra Diaz H.T.
IHC Department, HMFW
The information contained in this message and a
Does anyone out there have any Spirochete Control tissue they would be willing
to trade or sell?
Thanks!
Jenny
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I use Leica cover slipper it is great, never gives problem
Mesruh
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On Nov 25, 2011, at 1:00 PM, histonet-requ...@lists.utsouthwestern.edu wrote:
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Is anyone using Arginase 1 on the Bond system? Where are you purchasing this
from? Is it staining well?
Thanks
Nancy
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