Hello Karen,
Back in the old days of doing IHC manually on mostly fresh, frozen tissue I
would immediately place the slide with the frozen section into a coplin jar of
acetone to fix it. Keep the coplin jar of acetone in the cryostat. Leave it
in the acetone for only 10 minutes. Try
I agree with Barbara try fixing in cold acetone/ethanol mix even = if
just for a couple of minutes then go directly to buffer do not dry
after= fix, I would dilute the protease 1:4 with buffer (PBS or TBS
what ever u u= se) and do it for a short time. Enzyme digestion on
Thanks for the reply,
We are pre-fixing in a formalin substitute, but we'll give the acetone a try.
I have diluted the protease, but have not gotten any good results. We'll keep
trying with that as well.
We've tried multiple incubation times for the cytokeratin... From 5 minutes all
the way
I have tried this method as well and it works just as described below.
Sarah E. Lewis HT, ASCP
The Research Institute at
Nationwide Children's Hospital
Center for Gene Therapy
Neuromuscular Division
Rm WA3110
(614)722-2204
-Original Message-
From: Tony Reilly
Hi Karen,
It could be that your cytokeratin antibody only recognizes a formalin fixed
epitope conformation and enzyme digestion has nothing to do with it. Also try
fixing in formalin and then try the stain again with and without the diluted
enzyme digestion. Brief antigen retrieval (Citrate
Hello All,
A question was posed to me by our Cancer Resource Department...
I am wondering if you/lab has had experience with shipping tissue specimens
outside the country. We have a study where we may be doing this and they are
asking if we have to have a special permit to ship outside our
Hi All,
Does anybody have a protocol for Gram stain on FFPE mouse intestine
sections. We are looking to distinguish between Klebsiella and Vancomycin
Resistant Enterococcus (VRE). I would like to avoid using Picric acid as
some protocols suggest.
Thanks in advance.
Hi Ventana-users,
we have a special technical problem with our Ultra. It seems, that the
liquid in the waste-tube is sometime pressed out of the hole on the platform
like a fountain.
You can imagine the nice surprise, when the oil drops from the Ultra-roof
onto the carousel-top. Everything is
What detection kit are you using?
Sent from my iPhone
On Oct 2, 2013, at 10:47 AM, Bauer, Karen L. bauer.ka...@mayo.edu wrote:
Thanks for the reply,
We are pre-fixing in a formalin substitute, but we'll give the acetone a try.
I have diluted the protease, but have not gotten any good
In less than 8 hours I can get 96 Ihc stains done with our dako link and that
is two runs
Sent from my iPhone
On Oct 1, 2013, at 1:15 PM, McKenzie, Emily mckenzie.em...@mhsil.com wrote:
Hello all,
I am currently working on a Six Sigma Green Belt project and am looking for
some data. Can
We have had great success with the Twort gram stain.
From: Mesru T turke...@gmail.com
To: histonet@lists.utsouthwestern.edu
Date: 10/02/2013 10:13 AM
Subject:[Histonet] Gram stain
Sent by:histonet-boun...@lists.utsouthwestern.edu
Hi All,
Does anybody have a
Hi
Im looking for an acid phosphatase enzyme procedure that might be out there the
one we tried in the past was difficult to work up and get good reproducible
results.
Thanks
Helene D
Upstate University Medical
Syracuse, NY
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Histonet mailing
I am thinking there has to be a way to integrate the Validation into the
Optimization the vendor does. I think you should be able to make microarray
blocks/slides of at least 10 positive and more for ERPR per CAP during the
optimization. Now, the vendor will say they only do Optimization, but
Does anyone have an extra lever clamp for a Leica microtome? I'd be happy to
pay for it, and of course, for shipping!
Thanks,
Patty Lott
UAB CMBD Core Lab
205-934-2007
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According to our Receiving department, each country/institution has its own
permit requirements for receiving samples from outside of their own
country. It is up to the shipper to inquire of the receiver as to what
permits are needed to ship to that country (Germany, in your case). My
source
Needing a Histotechnologist (ASCP, QIHC certified) or Scientist
(Histopathology) for a Seattle area. Five years of experience in routine
histology including special stains, IHC and pathology knowledge. Send an
updated resume to yli...@numirabio.com to be considered. A full job
description
Dear friends,
I recall hearing at a conference (or maybe it was just a casual conversation by
an expert during a NSH symposium break) that vacuum and pressure in tissue
processing really accomplishes very little. I do believe that using heat and
agitation of the solutions provides more
Please share protocol for Triview from Zetta Corporation for Venatna.
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Hello All,
I have a Leica Cryocut 1800 with a Reichert-Jung 2020 microtome that has sat
for 8 years and went through a move from one academic building to another. I
am trying to section brook trout brain, but am having difficulty getting
consistent sections.
I will get a good section and then
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