Hello Histonet,
Our exclusively retained client has opened several new opportunities across
the U.S., and I wanted to reach out regarding a few specifics and see if
anyone would be interested in learning more.
Our client is a global leader in cancer diagnostics and we are looking for
individu
I would like to poll the Histo group concerning cytology specimens. The
discussion has come up about when to discard a fluid after processing,
and fluids that have no orders. Also, because we are a contracted
service for the hospital, and are not connected to their LIS. Cytology's
that are ordered
Hi Everyone,
I am trying to help out a coworker with a survey on types of tissue and
controls needed for both clinical and research labs. She has a short
deadline by next Monday.
She if in charge of the OriGene Technologies tissue division. If you could
take a few minutes to fill in the survey
UT Path located in the medical center (Houston) is currently looking for a
Medical Technologist that is able to work on an as needed basis, hours are
negotiable. Duties include, but not limited to performing molecular testing
using the Hologic Panther system, this could lead to a full time posit
Good Morning- can anyone give me a recommendation for a predilute PAX2
antibody? The one I was using has been discontinued and the replacement
product does not seem to perform very well. I will be using it on the Bond
III. Thanks in advance!
Jeff Robinson, Senior Histotechnologist, Sierra Pa
We keep our spill kits in unobstructed cabinets with bright yellow signage on
the wall above. We have no problem getting to them as needed, and have never
had an issue in many, many CAP inspections.
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Latest post:
http://www.chicagonow
What you need to do is to communicate to everybody where the kits are, and
place them where it is more convenient for you. Once everybody knows the
location, a good sign is always a plus.René
On Tuesday, June 14, 2016 10:15 AM, Anne Murvosh via Histonet
wrote:
Do spill kits need to be
It seems to me you are processing too much unless the slices are 3mm thick or
more.I suggest you to cut the dehydration to 45 minutes (the sequence seems
OK)Reduce the pure 2-propanol to just 2 changes (30 min is OK)Add 1 change of a
mixture 1:1 of 2-propanol and xylene + 2 xylene stepsthen to p
Good afternoon,
I am having a few issues getting nice morphology from both liver and heart
tissues. I currently work only with CNS tissues (brain, spinal cord, DRG,
etc.) but recently, our research team have become interested in
immunostaining some peripheral tissues, including the heart and liver
Do spill kits need to be out where anyone can see them, or can I put it in a
cupboard with a sign on the door? I need to move mine and there's very little
room. Thanks Anne
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Good morning everyone:
I seem to be having problems with over-processing of brain tissue.
I use a VIP6 processor.
I start off with 1 hour each of 30%, 50%, 80%, and 95% isopropanol.
Then half-hour each of three changes of absolute isopropanol.
Then half hour each of three changes of xylene.
Then h
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