Sorry, I should have included it.
ANP.22760 Are new lots of antibody and detection system reagents tested in
parallel with old lots? (NOTE: New lots of primary antibody and detection
system reagents must be compared to the previous lot using an appropriate panel
of control tissues.)
Mary Sue,
Our hospital regular releases gallstones to patients and/or their doctors. We
make a record of it in our computer system as to where and to who the
gallstones were sent/released to.
Karen Sly BS Biology
Pathology Department
Central Michigan Community Hospital
Mt Pleasant MI.
Please
Hi All,
Does anyone out there know a lab that is able to do a Human Herpes
Virus, Type 6 immuno?
Thanks for any help on this. We haven't been able to find a reference
lab that does this.
Carole
Carole Fields, HT (ASCP)
Histology Supervisor
Northside Hospital
Atlanta, GA 30342
carol.fie...@norths
Hi all,
How would you handle a request from a surgeon, f= or release of
gallstones or any tissue, to a patient? Assuming a 'Rele= ase of
Tissue' request form, indicating the biohazard staus of the tissue,is
signed by the patient, is this commom practice?
Thank
Jennifer,
What do you wish to accomplish histologically? Do you only wish to see the disc
material? Do you care about the cranial and caudal vertebral bodies? Are you
wanting to perform IHC? Please tell me a little more so that I can provide you
with a more detailed options. I am assuming t
Problem, if you store it in alcohol, you compromise the potential for IHC, and
other tests. It somehow messes with the antibodies.
But I am no expert Supposedly its why people switched to formalin fixation
instead of alcoholic fixatives
Maria Katleba MS HT(ASCP)
Pathology Dept. Mgr
Que
Reuel,
Do the opposite and turn up the temp on the waterbath and let the section float
out a little before the wax starts to break up. You can even gently use the
forcepts to tease out any folds and this will definitely help to release any
wrinkles in the cartilage. Then, make sure the sect
Sara,
Funny that this comes up now. I attended a meeting last week and this was
one of the topics. It was suggested that the tissue be stored in 70%
alcohol. I personally have not done this but I am going to start doing
this.
Beatrice Sullivan, HT(A.S.C.P.) HTL , AAS, CLSP(N.C.A.)
AP Supervisor
S
Sometimes placing them on a hot plate at about 60C will help get out the
folds, the paraffin needs to melt and the sections need to turn clear
then take it off the hot plate. If you leave it too long on the
hotplate the articular cartilage may fold over on itself.
Liz
Elizabeth A. Chlipala, BS,
Hello,
We are using our appropriate antibody control tissues run side by side to do
the antibody and detection system lot tests. One using the old lot number of
reagents and one with the new lot number of reagents.
TTYL,
Daryl Mikita, HT(ASCP)cm
Wyoming Medical Center
Anatomical Pathology
1233
Thank you all so much for the guidance! I appreciate all of the input.
Sincerely,
Cristi
From: Lee & Peggy Wenk
To: Jeff Birkner ; Rene J Buesa ;
Histo Net ; Cristi stephenson
Sent: Wed, June 16, 2010 6:18:15 PM
Subject: RE: [Histonet] alcohol monitoring
Y
Hi histonetters
Was wondering if anyone saw the new gui= delines for breast Cancer
specimen handling ? I am sure you have.&nbs= p; What my Pathologist
is wondering is if you have a large specimen and do = not use all the
tissue for processing what would the agent be
Hello histonetters especailly hard tissue group
I have a pig femoral head bone tissue embedded in paraffin and I have a hard
time getting rid of the folding problem. I tried to remedy by lowering my
temperature to 38 C and putting them in 5% alcohol before placing them in water
bath I still hav
Mike,
We have the Print Mate and 5 Slide Mates. We are not connected to our
LIS - we use it as a stand alone process. Everything is set up very
basic and the system works very well for us. Feel free to contact me
offline.
Laurie Colbert
Huntington Hospital
Pasadena, CA
(626) 397-8620
-Ori
Is anyone using the Thermo Slide Mate & Print Mate with CoPath as your
AP LIS? I am trying to decide if I am going to look at this as a stand
alone process or integrate it with my AP LIS. I would like to hear from
those that use it both ways and if it is okay to contact you off line.
Thanks,
Hi Brandy,
I have recently had the opportunity to build a Path lab from scratch.
In the design we decided to completely separate the grossing area from
the microtomy and IHC area of the lab. We built a "room within a room",
made it negative pressure, installed 2 Thermo elevating grossing
stations
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