Hi,
I want to destain hematoxylin (Shandon's Gill II). How to do that?
Thanks in advance,
V. Neubert
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Just want to buy some slides for our brain sections. Pre-fixed before cryostat
section.
normally 10 um -40 um.
Thanks very much !
s/#Disclaimer
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hello,
I was sarching for a paper from Journal of histotechnology. Unfortunately
the paper doesn't show up on medline and I can't seem to find an archive for J
Histotech that goes back that far. I wish somebody could help me .
The paper is: Okia, Zelda, Tihan, Tarik, Kane, Philip.
If you are a member of the NSH you can ask the article from them and they will
send you a pdf file
René J.
--- On Mon, 5/4/09, 伍治 woods1...@yahoo.cn wrote:
From: 伍治 woods1...@yahoo.cn
Subject: [Histonet] Journal of histotechnology paper searching
To: Histonet@lists.utsouthwestern.edu
Date:
Hello Histonetters,
The Louisiana Society for Histotechnology is pleased to announce
the 26th Annual Symposium/Convention:
Your Histeaux Surplus Package
June
We use Crystalmount. You don't even have to coverslip. Just make sure you
evenly distribute the mountant on the slide and let it dry. We usually put it
on a hot plate for a bit. This leaves a hardened shell around the tissue. The
slides can be read like this too. If you really need a coverslip,
We had a paraffin plug in the waste container, which caused a
malfunction of the unit and contamination of our reagents. We paid for
CBG to come out and perform and thorough PM before we used it again. We
have had the unit for about 7 or 8 years and this is the first time this
happened.
Laurie
Can someone provide me with the guidelines (Canadian) for scoring ER/PR
and what the preferred antibody is for determining this. I see there
are several clones.
Diana
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That makes sense. Know I can see where the processor may be responsible
for the carry over. This is a good thing to know if and when looking for
new tissue processors.
Mike
-Original Message-
From: Mark Tarango [mailto:marktara...@gmail.com]
Sent: Saturday, May
Would anyone be willing to share what they do for lab safety as far as
teaching, and keeping up with what is requested by CAP? Since I have chemicals,
I have been nominated to be in charge of the Chemical Hygiene manual which now
consists of all training for the lab and so forth. What are you
Hi All,
We have a morgue attendent who does not fit into the XXL gloves. Does
anyone know a vendor who can provide XXXL GLOVES latex (powder free)
prefered, but will take any other brand too.
I do really appreciate the help!
Thanks
Nirmala Srishan
Holy Name Hospital
Teaneck NJ 07666
1) Acid alcohol: I use several drops of concentrated HCL in 95% ethanol (1%
HCL in 70% alcohol well too). Simply dip your rinsed slides (or sections)
into solution a couple of times, rinse and check them... a dip in water with
about 10drops of ammonia should follow as well...
2) Saturated picric
Hello everyone!
I work with a scientist who insists on using primary antibodies directly
conjugated with FITC or Texas Red for IHC. In my past experience these
directly conjugated antibodies didn't give a strong enough signal for
use in IHC (I've seen them used only for FACS analysis). I
Any good HE stain will reveal the eosinophils.
René J.
--- On Mon, 5/4/09, Jan Shivers shive...@umn.edu wrote:
From: Jan Shivers shive...@umn.edu
Subject: [Histonet] (canine) eosinophil IHC
To: histonet histonet@lists.utsouthwestern.edu
Date: Monday, May 4, 2009, 3:41 PM
Hello all,
I'm asking
Acid alcohol. It may not remove all of it but it will remove the majority.
On Mon, May 4, 2009 at 5:32 AM, V. Neubert histonet.nos...@vneubert.comwrote:
Hi,
I want to destain hematoxylin (Shandon's Gill II). How to do that?
Thanks in advance,
V. Neubert
Jennifer,
In the past, upon occasion when need arose, I'd use directly conjugated primary
antibodies. Mainly biotin or dig or peroxidase but also FITC directly to
primary. Then can look at it fluorescently or come back with an anti-FITC of
some kind (several are good). Used these for my
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