I have also used this system and worked it up on the N
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210
From: histonet-boun...@lists.utsouthwestern.edu
Sorry email cut off. I worked it up on the Dako Autostainer Link 48.
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210
From: histonet-boun...@lists.utsouthwestern.edu
Good morning,
We are looking to purchase some little metal/stainless steel baskets
with expandable lids used for processing larger specimens. We just
found out EMS does not sell them anymore. Does anyone here in
histo-land know where we can find these?
Thanks in advance,
John
Hi Histonetters!!
Right Place, Right Time, Right Opportunity!
Sometimes your next career move is just a matter of being in the right place at
the right time and ready for the next opportunity.
Odds are that if you are contemplating a job change for whatever reason –
better compensation, a
I believe there is no chance for retrieval. DNA or RNA is degraded by
hydrochloric acid. You would need some glue to stick the fragments ;).
Gudrun
-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von
Everyone,
We are having a heck of a time orienting GI biopsies but esophageal biopsies in
particular, during embedding. If anyone could share their secret for getting
these tiny specks of semi-transparent tissue oriented, we would greatly
appreciate it.
Sabina Sylvest
Department of Pathology
There is a very fine Technical Note by I. Dimenstein in the last issue of the
JOH that can help you solve this problem.
René J.
--- On Thu, 9/24/09, ssylv...@cinci.rr.com ssylv...@cinci.rr.com wrote:
From: ssylv...@cinci.rr.com ssylv...@cinci.rr.com
Subject: [Histonet] Orienting GI biopsies
I've posted a number of times about the Histobath. I don't know
anything new besides the stuff I've already posted.
Melanie S. White, MT(ASCP) asks:
P.S. Are there any other Samurai Pathologists available? We need one.
Hey, find me a way to get a South Carolina medical license at the age
of 70
Sabina Sylvest at Cincinnati Children's Hospital asks:
We are having a heck of a time orienting GI biopsies but esophageal biopsies
in particular, during embedding. If anyone could share their secret for
getting these tiny specks of semi-transparent tissue oriented, we would
greatly appreciate
Hi, Would anyone using SOX10 antibody please tell me where they buy it? If
you have a procedure that you would be willing to share as well I would be very
appreciative. Thank you!
Erin Martin
UCSF Dermatopathology
___
Histonet mailing list
Does anyone have a protocol for the Steiner and Steiner stain that does
not use Uranyl Nitrate? Our EHS department will not allow us to order
this chemical anymore because it is too expensive to dispose of. If
anyone has any methods of disposal that are not too pricey I would be
interested in
Check with Newcomer Supply as they have a Modified Steiner Kit without
Uranyl Nitrate.
Jodie Robertson, HT(ASCP) QIHC
Pathology Sciences Medical Group
Histology Day Supervisor
Chico, CA 95926
-Original Message-
From:
I would like to share a room for the NSH Symposium/Convention in
Birmingham to help save on costs. I have a room reserved at DoubleTree
from Friday - Wednesday, but if you already have a room reserved and are
looking for someone to share costs, I can do that too.
Send me an email at
Not us!!
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Richard
Cartun
Sent: Thursday, September 24, 2009 13:38
To: Histonet
Subject: [Histonet] MSI testing
How many of you that do IHC and/or PCR testing
Hello,
I've tried a dozen times to get good fluorescent CD31 staining (endothelial
marker) on frozen mouse liver sections.
I'm using the standard pharmogen Anti-CD31 primary with a secondary FITC
label, and get a very weak (though noticable) signal.
My question is regarding
it seems when I use guniea pig-anti-doublecortin (DCX) with secondary antibody
from invitrogen goat-anti guinea pig Alexa 488 or 568. I always get staining on
blood vessel-like structures.
Anyone has such experiences before? Do goat-anti-guinea pig IgG will cross
react with rat IgG ?
Or
Two questions (if anyone can answer):
(1) What tests are you doing if you in fact have a 'molecular lab'?
(2) Who runs the tests...Histotech or CLS ?
Thanks!
Maria Katleba HT(ASCP), MS
Pathology Dept. Mgr.
Queen of the Valley Medical Center
707-294-9229 cell
707-252-4411 x3689
To all,
I would like to know what everyone is doing with the cap survay now that it is
scoring staining performance and not detremining a diagnosis. Our paths want
us to score then and they not be involved. Is this what everone else is doing?
Edie
DISCLAIMER:
This message is intended for
Technologists can certainly be trained to do the scoring properly but our
pathologists score them and are fully involved in the evaluations, as well as
reviewing challenge slides for submission. There are also sometimes
interpretation questions that have to be done on-line that the pathologists
Gudrun is absolutely correct. The HCl destroyed your nucleic acids. The best
decalcifier for RNA or DNA is EDTA.
Teri Johnson, HT(ASCP)QIHC
Managing Director Histology Facility
Stowers Institute for Medical Research
1000 E. 50th St.
Kansas City, MO 64110
Joyce,
You might have some luck calling the following places:
Physician's Reference Lab, Overland Park, KS - Donna Miller
Shawnee Mission Medical Center, Overland Park, KS
North Kansas City Hospital - N. KC, MO - Nancy Warren
University of Kansas Medical Center, Kansas City, KS - Timothy
I would appreciate comments from anyone using this fixative for bone marrow
cores. Specifically I am interested in learning how long you are fixing your
samples in B Plus.
Manufacturer recommends at least two hours but we are seeing artifacts that
concern me that 2 hrs may be insufficient.
I would recommend you try to embed them on edge.
Even if very small, you will be surprised how many are correctly
embedded
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at
Nikki,
The sensitisation step, from my experience, improves the silver
deposition on the bacteria and decreases background staining. Margeson
Chappman (1996 Use of Zinc Formalin as a Sensitizer in Silver Stains for
Spirochetes J Histotechnol 19(2):135-138) substituted zinc formalin for
uranyl
Edie,
What a challenge.
I would strongly recommend you give it a go.
I like to score fixation, processing and staining quality of slides I
and my staff produce.
It allows us to have control over the science of histotechnology not the
pathologists (they have enough to worry about - the diagnosis,
Hi all,
Just a note to say that I will be leaving next week for Birmingham
Alabama for the NSH conference.
It has taken me 30 years to get to a NSH and I am really looking forward
to it.
I hope to see you all (I will be the old, short, bald guy with the
Aussie accent)
Regards
Tony Henwood JP,
Hello!
I wonder if anyone knows if copper pigments can be stained in 3 micron FFPE
human liver core biopsies using a Rhodanine Copper staining method? The
procedure suggests 6- 8 microns. Our small amount of tissue core biopsies are
cut at 3 microns and if possible we would not like to cut
Dear Histonetters,
I think everyone on the Histonet would like to hear about all the creative,
cost effective, and HIPPA-compliant ways labs can dispose of slides and
blocks that have exceeded their retention limits.
Does anyone use an outside company that disposes of glass slides and/or
I am attempting to renew my HT ASCP certification for the first time and I
was wondering if taking the Anderson Continuing Education course (Molecular
Diagnostics: Fundamentals, Methods, and Clinical Applications-they list it
as providing 36 hours) would fulfill the requirement completely. I
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