We accept biopsies until 10:30 a.m. Monday through Friday. If it is an
extreme emergency, we will accept a later cut off time and someone stays to
take care of it. Yes, we will process transplant biopsies on weekends and
holidays. We do not process the biopsies at night.
Hazel Horn
Good morning,
I know all histotechs help cut and stain frozen sections. Is there any
organization out there that has the histotechnician gross the frozen section
tissue and place on the frozen section chuck to cut without the Pathologist in
the room. If anyone does this please tell me why?
You might try contacting Cell Signaling Technology in Danvers, MA. They
carry a rabbit mAb to ROS1 and I believe they have control slides that can be
used for validation purposes.
Richard
Richard W. Cartun, MS, PhD
Director, Histology Immunopathology
Director, Biospecimen Collection Programs
Is a candid control one that's taken when the fungus doesn't know you're
sampling it?
Sincerely?
Jay A Lundgren,
M.S., (HTL) ASCP
On Fri, Jan 10, 2014 at 11:58 AM, Webb, Dorothy L
I have one tech telling me that when the entire processor is changed the tissue
is too dry. We run a lot of fatty tissues, breast, etc on this processor. (Our
biopsies are run on a separate processor). Is this correct, or should we only
rotate reagents? No other techs complain. I have a hard
This depends on so many different factors, however, I prefer a frequent
rotation over a complete change.
Do what is best for your tissue!
Sent from my iPhone
On Jan 13, 2014, at 9:46 AM, Jb craiga...@gmail.com wrote:
I have one tech telling me that when the entire processor is changed the
This gets me back to another recent topic, soaking the blocks.
I've seen this a little in the past, just soak them on an ice block,tray for a
couple minutes and you'll be fine. To me, another indicator would be that if
you're getting dry tissue when changed but not later could there be some
Dear Histonetters,
I wonder if anyone has done myeloperoxidase stain on FFPE or frozen lung
sections?
I would appreciate any help.
Regards,
Mesru
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Fellow techs,
I have a per diem histo tech position in the Boston area. We are a
small uropath lab and the duties will include embedding, sectioning
and IHC's.
thanks,
Ron Martin
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Hi!
Can someone recommend literature about microwave processing. I'm interested
in the physical principles behind the process. And I want to get answers to
the questions: why is this microwave-assisted infiltration faster? What
happens to proteins /antigens under microwave radiation? Is there
Our pathologists prefer to perform all aspects of frozen section preparation.
We will stain for them, but they would rather gross and section themselves.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Perhaps you can get some literature from one of the vendors that sell that
technology.
Milestone Medical
Sakura
Walter Benton HT(ASCP)QIHC
Histology Supervisor
Chesapeake Urology Associates
806 Landmark Drive, Suite 127
Glen Burnie, MD 21061
443-471-5850 (Direct)
410-768-5961 (Lab)
This is the only way that a non-pathologist can gross tissue, whether
for frozen section or otherwise. They must meet CLIA standards for high
complexity testing and furthermore, CAP says that the exact nature of
the tissue grossed must be spelled out, along with nature of the
pathologists'
Gudrun,
A good overview is here: http://www.ebsciences.com/papers/mw_tech.htm
A couple old books:
The Microwave Cookbook for Microscopists, Boon and Kok
Microwave Applications in Pathology [Hardcover]
Anthony S. -Y Leong
This person also wrote a lot of articles back in the 1980's and
Hi Gudrun:
I recommend you to get The Microwave tool book by Login and Dvorak (1994) I
am also sending you under separate cover an article I wrote on the subject.
As to your questions, the practice of histology has concluded that:
1- the physical principle is that microwaves excite (shake) all
Actively looking to purchase - possibly two, in good condition. Thanks Vicki @
608-262-8534
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Yep,
We use a rtu from Leica on the Bond3 platform (PA0491) with EDTA (high pH)
antigen retrieval
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager Senior Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University
Hello histonetters!
Could I please get some help/advice/ideas on how to reduce recut/deeper
requests? What does your lab do to reduce that? Would you say embedding is
partially the problem? Such as small tissue embedded with bigger tissue? Etc?
What are the reasons they ask for recuts? The answer to that will give you some
ideas. For instance, did they not get a full face with margins the first time?
Was the section not readable? Was the stain inadequate?
Tim Morken
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