Hi All,
I am searching for a disposable blade holder for an older cryostat. It is
a Heidelberg HM 500 (Microm).
Thanks,
Jennifer MacDonald
Mt. San Antonio College
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Hello,
I need some help on how to remove the sucrose from mouse eye balls also I need
a good protocol for fixation and sectioning of mouse eye balls (without
detaching the retina from the rest of the eye section) for Immunohistochemical
staining.
Any help I would really appreciate it
Thank you
You mean chemical / fire shower?
Our hospital has a guy test it once a month and record it. And record on a tag
on the shower the date it was tested?
Tim Morken
UCSF PATHOLOGY
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From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwest
Does anyone have a QC log on the yearly fire shower testing they'd like to
share?
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Could I get some feedback on linear stainers?Has anyone had any
experience with the Leica ST4020?
We are going to purchase a linear stainer for a new MOHS laboratory.
Thanks,
Sandy Harrison
Histology Supervisor
VA Health Care Systems, Minneapolis
612-467-2449
_
We have it documented within the APLIS, when the order is placed within our
EMR,, for requisitions we have them document them on the requisition at the
time it is taking place with a sticker,, but since the most of our orders are
electronic it is part of the workflow, this is done for all specim
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Our OR and Breast Health staff have done pretty well getting on board with
this. We rarely have one that hasn't been documented.
We have a place on the requisition (located just under the date field so they
will see it) where time out of body (for the cold ischemic time), and time into
formal
Hello everyone,
Can you please share with me the EGFR primary antibody you use and what
pretreatment you use with itthanks in advance!!
Colleen Forster
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I just read on the Arraymold website that I am probably using the wrong type of
paraffin for constructing my TMAs. I used Richard Allen Type 9 but they
recommend Paraplast X-TRA from Leica or Blue Ribbon from Surgipath. I hope a
different paraffin solves the issues.
We have a label that we place on the original requisition documenting
the time the specimen was placed in formalin and the time it came out of
formalin(changed stations on tissue processor). When the
transcriptionist
transcribe the gross dictation they give the total number of hours the
specimen
Probably the paraffin wax surrounding the cores has not infiltrated them
perfectly and you have ended with a TMA block that cannot hold the cores
adequately.
My suggestion is to melt the block again and leave the cores in melted paraffin
during at least 1 hour and prepare new blocks that will ha
We constructed some TMAs for Validations and when I tried to section the TMA
blocks the sections shred. It's really hard to get a nice ribbon or even a
nice section. I don't know what I am doing wrong. Has anyone had problems
cutting TMAs before? Any solutions? We are using the Arraymold i
Earlier I submitted a question to histonet to ask about labels that
can be used to bind bone at the site of bone formation in aquatic
amphibians. Robert Schoonhoven kindly sent a response stating that
tetracycline has been used in mammalian systems. I also recently
found a paper (citation
We have recently moved to printed/barcoded labels for all of our slides. Each
pathologist has a mnemonic in our LIS (Meditech) that we use when assigning the
case. This mnemonic is picked up and printed on the slide label.
It has been a real help, especially on recuts and stains. We no longer
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