In Newfoundland Canada the scale is $32-42 / hour.
Elizabeth
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Hello Histonetters,
Anyone have a spirochete control block(s) they would like to trade?
Thanks,
Tim
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In my experience with the Leica coverslipper, I have to hand coverslip all
Ventana slides. It throws more than it coverslips. I have tried running them
down quickly and avoiding Xylene on the labels, but that works only marginally
better.
Ashley Troutman BS, HT(ASCP) QIHC
Does anyone have a go to stain for Mast Cells besides Tol Blue? We are
trying to demonstrate the presence of mast cells in human arteries ffpe.
Also, what would be a good positive control to use for mast cell staining,
we used NH Skin and got maybe a few mast cells but I would like to use
I use histoclear in the last step of dehydration and have no problem with
the arm picking up the slides. If I leave the slides for more than one hour
in the last histoclear and if the histoclear covers the labels, then the
glue of the label dissolves and interferes with the arm picking up the
I have an opening position for histotech.This is a full time and permanent
position; if you are interested please call me or e-mail your resume. Thanks
Tunde Ajibade BS, HTL(ASCP)QIHC
Histology Supervisor
Medical Center Hospital
Odessa,TX
Email:tajib...@echd.org
Tel:432-640-2348
Go to http://stainsfile.info/StainsFile/stain/cell/aldtolblue.htm for a
reliable method. It still uses toluidine blue, but the staining is not
based on metachromasia and mast cell granules are dark blue. Most
toluidine blue samples will work, but occasionally one doesn't. Fisher
brand is OK as
I use to have a problem with the labels from the Ventana slides on the
Leica Coverslipper. I now use the Trubond 200 slides which are a little
wider (76x26mm instead of the standard 76x25mm) this keeps the labels
from hanging off the sides and it seems to work on the Leica
Coverslipper.
Sandra
During residency, we prepared frozen sections by placing OCT and tissue on a
precooled specimen disc and then putting a heat extractor on top, which both
rapidly froze the tissue and created a flat surface.
This seemed to work best when the heat extractor was slightly larger in
diameter than
A good one that I used to use was the Naphthol AS-D Chloroacetate-esterase
which stains the non specific esterase activity in mast cells. It is a
pain to run, but it is one of the most beautiful. A bright red mast cell
against a pale background. We got it from Vacca, p 530-533.
On Tue, Nov 1,
Igor,
I perform Mohs which is a frozen section procedure. There are a couple of
things that could help you. You do not have to leave the slides out to
airdry for an HE only do this is a specfic procedure requires it. Do not
places slides strait into water. As Kim, stated some people use a
I am out of the office until 11/07/2011.
I will respond to your message when I return. If you need immediate
assistance please contact 800-248-0123 or
tech.supp...@leica-microsystems.com
Note: This is an automated response to your message Histonet Digest, Vol
96, Issue 1 sent on 11/1/2011
Our tissues are frozen in OCT. I use Super Frost Plus slides from Thermo
Scientific and store the sections in the fridge until I need them. After
leaving them out on the bench for an hour I start my HE with 1 min running
water and so on. I rarely lose sections with these slides.
Daniela
Has anyone had good results staining for luciferase in FFPE tissue? If
so, what antibody did you use.
Thanks!!
Julie
Julie Randolph-Habecker, Ph.D.
Director, Experimental Histopathology Shared Resources
Fred Hutchinson Cancer Research Center
1100 Fairview Ave N, DE-360
Seattle WA
may I ask why you are not fixing them? Even the stain the 1st gentlman was
doing(Beta Gal) recomended to have a formalin fixation apllied first.
There are many ways to get to the same show as we all know, But in my
experiance air drying frozen sections will dry out and cells can autolyse as
You have to soak it in holy water, then all H311 will break out
Sorry, I couldnt resist.
From: Randolph-Habecker, Julie jhabe...@fhcrc.org
To: histonet@lists.utsouthwestern.edu
Sent: Tuesday, November 1, 2011 6:49 PM
Subject: [Histonet] Luciferase IHC
Hi all,
Is it possible to do an immuno with DAB detection and counterstain it
with alcian blue at the end to detect Goblets cells? I've tried it and
the DAB disappears under the staining.
Thanks,
Daniela
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