I am taking a chance that this is still a working email!! I came across an
old post on histonet regarding Xylene subs with a linear stainer. I was
wondering if you made the switch, and if so could you share the brand and
your H&E protocol. I have had some issues with Eosin bleeding, slides very
eo
You can contract for services to another lab or hospital and depending
upon the terms of the contract, you may be able to bill the patient.
For example, you send all of your HER2's and ER/PR to another lab to be
stained and quantified into a score. You may contract with the other
lab for them to c
Hi,
I do hope you are looking at cross sections of the wing and not the
flat. That would be very difficult indeed. For good cross sections I would
try a "Swiss Roll". This is a way of demonstrating a large amount of cross
sectional area in small space. Take the membrane and fix it by submersion
Does anyone know where I can obtain the MIN6 beta cell line derived from mouse
pancreas? They are listed and used in many papers but do not list the source. I
have tried ATCC and suggested cell banks in ECACC (England), DSMZ (Germany),
and JCRB (Japan) but they are not listed.
Thanks,
Page
I will be out of the office starting 07/02/2010 and will not return until
07/13/2010.
Please contact Kelly Miner at 617-871-5122 if you have any questions
regarding clinical trial samples.
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Histonet@lists.utsouthwestern.edu
htt
Hall's bile stain - not really a stain but a reaction, like the Perls
prussian blue reaction for iron - uses trichloracetic acid and ferric
chloride to oxidize yellow-brown bilirubin to bright green biliverdin.
Or so I've been told - I've never seen one.
Something I've wondered about for a long ti
We have a contract with the hospitals, this comes from our billing manger.
We bill the hospitals, then they bill the patient.
Cindy Pyse, CLT, HT (ASCP)
Histology Supervisor
X-Cell Laboratories
e-mail cp...@x-celllab.com
-Original Message-
From: histonet-boun...@lists.utsouthwestern.ed
This paper can also be downloaded, indirectly, from the CAP's website:
_http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165-134.7.e48_
(http://www.archivesofpathology.org/doi/pdf/10.1043/1543-2165-134.7.e48)
Happy (re-)validating,
Joe
--
Message: 12
D
Histonetters:
If you do some work for another hospital (Histology) can you bill the hospital
or do you have to bill the patient directly? Is there a statute or Regulation
out there about this?
Thanks
Pathology Supervisor
Kathy Baldwin, SCT (ASCP)
Memorial Hospital and Health Care Center
sbald..
SuSa has a high mercuric chloride content, and tissues fixed in high mercury
fixatives do not require secondary fixation in picric acid (Bouin). The
mercuric chloride fixes in a manner which improves staining with acid dyes.
For Masson's trichrome on tissues fixed with simple formalin variants
In a recent article written by 4 pathologists, including Dr. Elizabeth Hammon
and Dr. Patrick Fitzgibbons, the recommendations are now including testing with
a lab that has validated it's assay against clinical outcomes. How is everyone
planning on fulfilling this requirement inasmuch as we are
Bouin's is used as a mordant in this stain.
Beatrice Sullivan, HT(A.S.C.P.) HTL , AAS, CLSP(N.C.A.)
AP Supervisor
Shore Memorial Hospital
609-653-3590
mohamed abd el
hi all
i'm going to stain some slides of small intestin which were fixed in susa.
i'm going to stain it by Massons trichrome.
i have read that slides should be secondry fixed in Bouin's or saturated picric
solution.
does it mean fixation of processed tissue after cutting with microtom??
how lo
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