Good morning all. I am in the process of designing a new lab. We have grown
beyond our walls and will be moving to a new building. If anyone has any great
suggestions or ideas they would like to share I'd love your input!
I'm still looking for a couple of tech too!
Thanks,
Linda
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Good Morning,
Our team here at Personify has recently been partnered with a World Leader
in Cancer Diagnostics who is going through a large expansion due to their
recent and continued success in the Immunohistochemistry market. Due to this
expansion we are currently seeking Histotechs who
Congratulations on your move to a new building and the opportunity to
have a fresh start in a new lab.
The first thing I would suggest is to NOT blindly depend on a laboratory
design firm to design your lab. Consider the design and operation of
your new lab like you would buying a new car.
Thanks. I am going to try that ice rink: tip. :-)
What I do to keep my blocks from sliding all over the place now is put a
kimwipe on my wet ice. They can cool and I also like to hydrate my blocks
a little. I feel it gives me a better looking section histologically. my 2
cents as well. ;o)
Happy Monday Histonetters,
I'm wondering if anyone can share a protocol for running SOX-10 on the Ventana
BenchmarkXT?
(On FFPE tissue)
Thanks,
Angie
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I section EDTA-decalcified mouse tibias frequently, and I find it helps if the
paraffin is very very cold during sectioning - if the tissue starts shredding
again, I press a large piece of ice to the block for a minute to cool it down
without having to remove the block from the microtome. It
Hello Everyone,
We are in the process of working up Napsin A. I was wondering what tissue
others are using for multi tissue blocks to validate the anitbody? Thanks,
Jessica Piche-Grocki, HT(ASCP)
Waterbury Hospital, CT
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Hi Linda,
We designed one from scratch without having a previous Path Lab in the
hospital before. We are doing a workshop to that end at NSH in Seattle
(WS 50). If you cannot attend the workshop, I will be happy to help in
any that I can.
Steve
-Original Message-
From:
Thanks Tim!
Steve
-Original Message-
From: Podawiltz, Thomas [mailto:tpodawi...@lrgh.org]
Sent: Monday, September 13, 2010 12:38 PM
To: Feher, Stephen; Blazek, Linda; Histonet
Subject: RE: [Histonet] new lab design
FYI,
I have been to Steve's lab. They have a great layout. A lot of
FYI,
I have been to Steve's lab. They have a great layout. A lot of time and effort
was spent in the design of it and it shows.
Tom Podawiltz HT (ASCP)
Histology Section Head/Laboratory Safety Officer
LRGHealthcare
603-524-3211 ext: 3220
-Original Message-
From:
Steve's workshop at NSH last year was a good intro to lab design. The most
significant take-away was that they did many, many modifications on paper
before they ever did anything for real...and all with LEAN principle driving
the design.
Tim Morken
Supervisor, Histology, IPOX
UCSF Medical
We are using a Lung Adenocarcinoma as a daily control. Although I have noticed
that normal lung macrophages will pick it up.
We ran our validation of the antibody using a multi tumor block (contains
various tumors from various organs) and a multi normal tissue block to ensure
that it stained
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Herrick,
James L. (Jim)
Sent: Friday, September 10, 2010 2:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Liver Processing Question
Hello
We recently built our new facility from the ground up. Having worked in
various histology labs, I knew what works and what doesn't work. Planning
the lab around work-flow is crucial. I started the design by simply writing
the name of each room I wanted constructed on a sticky-note. These were
Hi Loralee,
Thanks for your response. What did you use for the multi normal tissue block?
Kidney?
Also for the multi-tumor block did you just use tumors from organs that you
knew were negative for Napsin or did you use both positive and negative tumors?
Thanks,
Jessica
I am using aqueous mounting media, faramount, for the first time. The slides
I coverslipped several days ago look dry. Will soaking in water remove the
coverslip?
Margaret Perry HT(ASCP)
Dept of Veterinary and Biomedical services
Box 2175
South Dakota State University
Brookings SD 57007
Hi Jessica,
Our control for this antibody is normal lung, adenocarcinoma of the lung,
and thyroid. We use this same block for other stains too (TTF-1,
sufactant-A, EMA, etc.) but if I were going to make a control block specific
for this antibody, I would want to include a squamous cell carcinoma
Timothy,
We have the B/R 9700 ProCycler to recycle alcohol, xylene, and formalin. The
Advantage must be a newer model. About 70 gal of alcohol, 40 gal of xylene,
and 20 gal of formalin is recycled every 3 months. This recycler is easy to
use and works well for us. As with any equipment, you
We are just getting started with our Digital slide scanner and I am looking for
help. Anything you would be willing to share in terms of SOPs, Policies in
regards to CAP and validation forms used when you are initially validation the
machine would be helpful.
Thanks,
Mighnon Lashus, HT (ASCP)
Hi Histonetters,
I need some advice as my group is tasked to procure tissue from surgery sites
off-campus. Logistics within those other hospitals
do not allow a liquid nitrogen source, and my health and safety folks have
asked us to consider using a Dry Shippers or cryoport for snap
Thanks to everyone who gave some input on the X50, it helped a lot and has me
thinking twice about that particular piece of equipment.
Carlos
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