Does anyone know of any similar IHC courses on the east coast? I'd love to
attend this one, but won't be able to swing the travel costs. Thanks!
Message: 1
Date: Tue, 14 Jan 2014 08:41:40 -0800
From: Workshop IHC workshop...@gmail.com
Subject: [Histonet] IHC wet workshop anouncement
To:
Classification: UNCLASSIFIED
Caveats: NONE
Hi LeAnn, Please note my response below.
-Original Message-
From: Bassett, Juan L CTR (US)
Sent: Wednesday, January 15, 2014 7:39 AM
To: 'Michael LaFriniere'
Cc: 'stonet-boun...@lists.utsouthwestern.edu'
Subject: RE: Frozen sections
Hi Juan,
I am not sure of any ASCP guidelines nor jurisdiction over CLIA requirements.
It is my understanding all US laboratories have to follow the CLIA set
guidelines for performing all laboratory testing. Qualified HT or HTLs can
gross complicated (high Complexity) testing under specific
Thank you so much. These tips seem very helpful. Could you give me your
protocol? Times in temps in the impregnation step. And your measurements for
each reagent in the developing solution. I use acidulated water and I usually
get the pH at about 3.8. I am staining for h.Pylori. Like I
I need to do FISH with the universal bacterial probe EUB338. I am not
too familiar with FISH. Can we fix the sample with NBF or is 4%
paraformaldehyde better? The samples are acellular dermal matrix. A
quick lit search shows people using 4% paraformaldehyde, but the
histologist that will be
I just wanted to see what others in the histology world might be experiencing.
We have seen a marked increase in the percentage of HER2 cases resulting as
Indeterminate, when
we compare our last year patient predictive marker results to this year's
results.
The clone we are using is CB11 from
That is an interesting observation, as we have seen something of the same thing
and we use the Dako Herceptest.I would be interested in hearing others
responses as well. Thank you for asking the question.
Martha Ward, MT (ASCP) QIHC
Manager
Molecular Diagnostics Lab
Medical Center
Consider the ASCO-CAP guideline and scoring changes for Her2/ FISH, not sure of
the timeframe for your trend in increased positives, but my pathologist has
indicated that I should expect more positive and equivocal cases, so perhaps
related to categorizing of DX, rather performance or clone
This is my first time working in a GLP/GMP lab, Ive only been here for 6
months.
We cut a variety of tissue. At trimming is where they decide what tissue to go
in what cassette and so one cassete could have 4-6 different types of tissue.
And on the other hand we do osteoinduction studies, and
I am looking for a procedure and product to use for decontamination after a
potential TB case, help please!
Tanya G. Abbott RT (CSMLS)
Manager Technologist, Histology/Cytology
St. Joseph Medical Center
Reading, PA 19603-0316
ph 610-378-2635
fax 610-898-5871
email: tanyaabb...@catholichealth.net
Hello,
I know this subject had been looked at many times. I just want to see if I am
correct before I start doing anything different.
1. 88342 , not much change . We can still just bill once per site, per case.
This is per single antibody per Specimen. If I have a case with two parts and
Need to decon my cryostat
Tanya G. Abbott RT (CSMLS)
Manager Technologist, Histology/Cytology
St. Joseph Medical Center
Reading, PA 19603-0316
ph 610-378-2635
fax 610-898-5871
email: tanyaabb...@catholichealth.net
This electronic mail and any attached documents are intended solely for the
I am new to MMA plastic bone technique. Some one gave me his protocol, in which
has NaOH and d-water to wash MMA mixture before drying it in CaCl2. But others
told me I don't need to do the destabilization step. Could any expert in this
area to tell me if this step is necessary? And why have to
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