Liz,
Could it be due to the presence of residual wash water or previous solution
diluting the stain to give patchiness? On the same thread, insufficient
agitation of the slides in the solutions? You do not say if staining is by
hand or automated as this may be a contributor.
Whilst I have no
I have had this problem on a GI recut!! The first time through, the staining
was perfect. The pathologist requested recuts, and I was cutting surgicals, so
I put it in the back of the line up on my already melting ice bath to cut
later. The recut was terrible. Nuclear staining was very weak!
I would also be interested in the answers to this.
Cindy
Cindy Pyse, CLT, HT (ASCP)
Laboratory Manager
X-Cell Laboratories
20 Northpointe Parkway Suite 100
Amherst, NY 14228
716-250-9235 etx. 232
e-mail cp...@x-celllab.com
-Original Message-
From:
Hi Everyone,
Years ago, my lab used to put eosin in the processor to lightly tint the
smaller mouse tissues. I can't remember which station we put it in (I think it
was the 2nd 100% ethanol). Also, back then my lab didn't do any IHC; will the
eosin affect any IHC that might be done (I am
Good morning,
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Hi Histo World,
We are currently looking at how we process cell blocks and were wondering if
anyone had a procedure they would be willing to share with us. Currently, we
spin the fluids down in formalin and put the entire button in a biowrap and
process that. This leaves our cell blocks very
Need help please..does anyone have a colon block, or would be will ing to
cut me a few slides of colon, that has stained positive (which is actually no
staining) for the MSI antibodies; MLH1,PMS2, MSH6, MSH2 ?
Thanks!
Kenia Lynch, M.T./H.T.
Histology/Molecular Supervisor
Caldwell
The only immunostaining any residual eosin in tissue might affect is if you
do immunofluorescence. Eosin does fluoresce. Others can address any
effect on IHC.
Gayle Callis
HTL/HT/MT(ASCP)
Bozeman MT
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Eosin won't interfere with binding of antibodies, but eosin is
fluorescent. You might want to consider that.
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Histologist needed in Austin TX
We have a full time day position opened for a HT or HTL (ASCP) registered
histologist; requires 3 years experience and strong embedding and cutting
skills. Experience in muscle enzymes, EM and IHC preferred. If you are
interested in learning new techniques
With different products the toxicity level will vary. Write in the diamond the
highest toxic level even if that is not the most abundant.
By doing so you cover all inside the drum regarding their toxicity. I do not
see the need for the emergency phone but if they told you to so so, do it.
René
Hi Kim,
try 10cc of the prediluted Eosin (you use in H E staining) in your last 100%
before your Xylene on the processor. By putting it in the last absolute it will
not wash out. Your first Xylene will end up a little pink but your eyes will
not strain as much trying to fine the tiny tissue
Eosin on processor can be done with dirty eosin waste saved from the stainer;
adding eosin powder sounds like a mess.
Especially helpful for orienting small samples with a sidedness, skin GI GU
oral, cornea
No common down sides for routine HE, PAS, Trichrome, or IHC even with Red
chromagens.
We
Looking for a reference lab offering the above.
Thanks,
Linda A. Sebree
University of Wisconsin Hospital Clinics
IHC/ISH Laboratory
600 Highland Ave.
Madison, WI 53792
(608)265-6596
FAX: (608)262-7174
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You might want to try www.phylogenyinc.com.
On Nov 28, 2012, at 10:54 AM, Sebree Linda A lseb...@uwhealth.org wrote:
Looking for a reference lab offering the above.
Thanks,
Linda A. Sebree
University of Wisconsin Hospital Clinics
IHC/ISH Laboratory
600 Highland Ave.
Madison, WI
Hi Histonetters!!
I hope you are having a great day. I have a quick question. Is ASCP
certification required in order to work in the state of Michigan?
Happy Holidays !!
Thank You!
Pam Barker
President/Senior Recruiting Specialist-Histology
RELIA Solutions
Specialists in Allied Healthcare
Supposedly eosin used to color small specimens, or put in the
processor, fluoresces enough in tissue sections to interfere with
fluorescent stains.
I've seen safranin O (from the microbiology lab) used to mark small
surgical specimens like GI biopsies. I don't know whether you can put
it in the
This morning I decided to pH our DI water, which came out higher than it
should. I then did an experiment where I cut a kidney and floated it on three
water baths - one a bit basic, one a bit acidic, and one neutral. I cut two
sections for each waterbath - one was picked up right away, and
Does anyone know what the CAP is requiring to validate a new tissue processor?
Thank You
Helena Howe
ProMedica Laboratories
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Hope you had a great Thanksgiving!
I am currently working on multiple openings in the tri-state area:
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NY
Histology Supervisor w Hospital Hartford CT
Histology Supervisor
Quick question for Histoland. I am having a debate about DAB disposal. Our
general manager ( non lab background) insists that the liquid DAB can go
into a biological hazardous waste. I disagree, it is a chemical and needs to
be disposed in the chemical hazardous waste. What is everyone else doing
It should be separate.
Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org
www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA 30342
This e-mail, including any attachments is the property of Saint Joseph's
Hospital and is
Great full time opportunity for a Histotechnician in Yuba City! North Valley
GI is looking for certified HT or HTL to join their laboratory . HT
candidate must meet the following criteria:
* Meet CLIA Grossing Requirements : CFR 493.1489,
http://wwwn.cdc.gov/clia/regs/toc.aspx/
Chemical hazardous waste.
Sent from my iPhone
On Nov 28, 2012, at 12:44 PM, Cynthia Pyse cp...@x-celllab.com wrote:
Quick question for Histoland. I am having a debate about DAB disposal. Our
general manager ( non lab background) insists that the liquid DAB can go
into a biological hazardous
You are right and your general manager is wrong (as they usually are when
dealing with histology issues!).
René J.
From: Cynthia Pyse cp...@x-celllab.com
To: histonet@lists.utsouthwestern.edu
Sent: Wednesday, November 28, 2012 3:44 PM
Subject: [Histonet] chemical disposal
Quick question for
You will also need to validate all of the IHC stains and special stains that
you do on these tissues. You can take samples from each tissue type and run
them in parallel on both machines. Then test all of your special stains and
antibodies that you have in your inventory.
:)
Helen
I have an investigator wanting to make microarrays from some frozen OCT blocks.
I seem to remember reading a way to do this. Can someone please point me in the
right direction?
Thanks
Donna Reynolds, HT (ASCP) Chief IHC Core Lab
Dept. Cancer Biology,
Univ. Tex. M.D. Anderson Cancer Center
I don't think it is necessary to test every single stain or antibody you do to
validate a new tissue processor. Most of the time the only thing changing is
the machine, not the chemicals you use. The point of validation is to prove
that the system gives you the same results as the old
Separate and chemical hazardous waste!
Steven Mello,HT(ASCP)
Sent from my iPad
On Nov 28, 2012, at 4:48 PM, Rene J Buesa rjbu...@yahoo.com wrote:
You are right and your general manager is wrong (as they usually are when
dealing with histology issues!).
René J.
From: Cynthia Pyse
We are a small pathology in the Sacramento area (Placerville) looking
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Hi All-
Looking for a happy person and a good cutter, preferrably the same person!
A short day shift temp, M-F from ASAP through the Friday before Christmas.
Fill up the bank account and be home for the holidays. Experience with small
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