Dear All,
I want to do immunofluorescence on formalin fixed paraffin sections, Can you
guys help me sending protocol how to do it ?
Thank you very much for your help.
BW
Anil
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1. Any feedback on the process for validating a new tissue processor? Finding
80 to 100 breast specimens that are large enough to divide up and retest
Estrogen and Progesterone would take a long time to complete. Also, how many
antibodies and specimens should be tested? As we all know, some
I am having to validate antibodies and was wondering if you have to do a
parallel study or just use known positive and negative tissue?
~Sabrina~
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I might also add that Neil Hand is co-speaking with myself and Philip Seifert
this year at the annual National Society for Histotechnology -
Symposium/Convention in Vancouver B.C. Our workshop is titled:
Resin Applications Forum: Methods for Processing, Special Staining,
Immunohistochemical
Becton-Dickinson Monoclonal antibody at 1:100 for 30 minutes after HIER
(citrate at pH6) with placenta as control.
René J.
--- On Mon, 3/12/12, Chakib Boussahmain chak_...@yahoo.com wrote:
From: Chakib Boussahmain chak_...@yahoo.com
Subject: [Histonet] CD34
To:
CAP has some guidelines as to the number of specimens and antibodies to test. I
think to remember that the lowest amount was 25 specimens, but I do not
remember about the antibodies but it makes sense to use only those your use to
work with.
René J.
--- On Tue, 3/13/12, Bliven, Laura
We also have a first generation Autostainer and I have had the same happen with
my machine. I believe it is definitely a mechanical issue. The engineer that
came out changed the motor driver unit and we haven't had a problem since. He
also told me that it can also be the belt drive on the
Google Color blind chart.
Then select images from the google menu.
You will get what you want.
Select the image and print on a color printer.
Viola! Done.
Stephen G. Ruby
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
You probably have to have someone administer it and verify it to make it
acceptable for CAP, though.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Stephen G. Ruby
Sent: Tuesday, March 13, 2012 11:37 AM
I will be out of the office starting 03/13/2012 and will not return until
03/19/2012.
Note: For Cytology issues, please call Molly at 8-421-5487, Eric at
8-421-5405, or Wanda 8-421-5426 For Histology / IHC issues, please call
Mario at 8-421-4961, Kiran at 8-421-5404, or general histology
Stacy Giroux (where?) asks: Our lab is currently transitioning from
the Brown Brenn gram stain due to no longer wanting to store picric
acid due to its potential hazards. Our pathologists have requested a
gram stain for paraffin embedded tissue that looks similar but does
not use picric acid or
Excellent! Happy to read the venerable Neil Hand is coming back to the
symposium, always a great speaker!
-Damien
On Tue, Mar 13, 2012 at 10:50 AM, Jack Ratliff ratliffj...@hotmail.comwrote:
I might also add that Neil Hand is co-speaking with myself and Philip
Seifert this year at the
Laurie asks: Does anyone know of any (free) online testing for
color blindness? Does anyone have an alternate method that they have
used to satisfy CAP requirements?
Here are some online Ishihara plates quickly found through Wikipedia:
Stacy,
I use a procedure that was published in the Journal of Histotechnology,
Vol 25, No2, June 2002. *Modifying the Modification: How to Redden Shy Gram
Negative.* It has worked for me consistently for many years without the
picric acid. It does use some acetone. I get the ragents from
You can switch to Tartrazine.
Nick Madary, HT/HTL(ASCP)QIHC
George Washington University
Pathology Core Laboratory
Ross Hall, Room 706
23rd and I Street NW
Washington D.C. 20037
202.994.8916
pat...@gwumc.edu
BEGIN:VCARD
VERSION:2.1
X-GWTYPE:USER
FN:Joseph Madary
I've been watching this thread with great interest I have been in
Histology for 30+ years now and am myself colorblind (at least according to the
Unites States Navy). I do see color even though I could not pass the old card
test (failed it 3 times). My problem is with shades of color. I
What a great story :-)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom McNemar
Sent: Tuesday, March 13, 2012 12:22 PM
To: 'Bob Richmond'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re:
Possible full-time position at a cancer diagnostic CLIA/CAP lab in San Diego:
Must be H.T.(ASCP)
Must have excellent cutting skills
Must have IHC experience (we use the BondMax)
LMD experience a plus or desire to learn (a must!)
prefer local candidate
email resume to:
paw...@yahooo.com
Hi,
I've read at a couple of places that you can't use the chemical test to
determine the end-point of decalcification if you used an ion-exchange resin
for the decalcification. I understand that calcium ions are captured by the
resin, therefore they can't be precipitated by the ammonium
Hello Techs,
I would like to get some feedback on the Dako Autostainer Link 48, using the
Flex reagents.
Thank you,
Cindy
Cynthia Bulmer HT(ASCP)QIHC
IHC Supervisor, CTPL
Waco, TX
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If you do that all the advantages of using the ion-exchange resin will be lost.
Simply determine the end point of the decalcification by other usual and more
traditional methods, like specimen bending or a pressure/penetration test.
You could also use X-ray with a Faxitron.
René J.
--- On Tue,
Looking for help againHas anyone been experiencing problems with the ink
printing coming off the Thermo Histoscreens after processing?
This information is confidential and intended solely for the use of the
individual or entity to whom it is addressed. If you have received this email
in
Happy almost Hump Day Everyone,
Does anyone use CPT code 88399 or 89240 for any type of unlisted or
miscellaneous pathology test or procedures? If so what type of test/procedures
are you using the code for?
Also is there a CPT code that can be used for gathering up pathology material
for
Greetings, friend!
http://metalgeek.zxq.net/response.php?urjluqjbahuma=79gjcewip=977ygoxab=38
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Almost exact same situation with me Tom. Navy refused my application for
Nuclear Engineering and made me a Medical Technologist instead. It
struck me as funny the first time I had to identify an eosiniphil. Then
I went to histolgy. Apparently the Navy didn't want me around things
that could
A long time ago I tried to use 88399 misc for prep work my techs were doing for
various test we sent out. We never got reimbursed for anything on that code.
Maybe others here had better luck than me with it. You seem to be thinking a
long the line I was about all the work we do that we don't
I love it. Great turn around time. Great crisp clean stains. And I think it's
easy to use. Some will say ah it has the off line Retrieval. But I like the
fact that the samples are submerged into a solution. Call me old fashioned?
I've used pretty much all of the platforms. They all have good
for those of you that use the ultraview alk phos red on their machines, do you
run the slides through
alcohols? we are having a lot of trouble with the staining, sometimes it is
good others no staining
at all on our mart 1s or pin4 prostate bxs.
I was told that we should not put them in
Hi everyone - Did I mention that Damien Laudier from Laudier Histology was a
guest last Sunday, March 11th on HistoTALK? Or that Vinnie Della Speranza from
MUSC Health will be our guest on Sunday, March 25th? No? Well, Damien Laudier
from Laudier Histology was a guest last Sunday, March 11th
I agree with Bob wholeheartedly as well as agree 100% and I am unanimous in
that!
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road
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