Does anyone know a retic stain that does not use uranyl nitrate?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Hi Histonetters,
I am having a very hard time in setting up the MDM-2 antibody on our Ventana
Benchmark XT's. I am using clone SMP14 from Becton Dickinson, which was working
fine on the Labvision. I have tried everything (even incubating overnight at
4ºC) and I am out of idea's. Maybe I should
Beautiful reply!
Sent from my iPhone
On May 29, 2012, at 4:58 PM, Cheryl tkngfl...@yahoo.com wrote:
Hi Ann-
May we assume you've confirmed this is happening at embedding and have ruled
out any floaters happening during cutting?
When embedding, keep Kimwipes or other tissues around,
Interesting thread about block alignment. Bernice makes a good point about
Newcomer's level, and the possible effects of benchtop or floor not being
level; perhaps the stage-mounted tools are preferable. We have a stage-mounted
tool, which brings me to another point.
Before this type of tool
Speaking of block alignment, when this topic comes up, someone invariably pipes
up... Hey, is your head on straight?
Eric
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
I find it sad that there are so many messages to unsubscribe following the
great certification debacle that has been on here the last couple of days. I
personally just find it tedious that on a server set up purely for histology is
where we are discussing whether or not histology is a
Haven't had that checked lately. How about you? I know my mom may have had
something to say to that effect back in high school..
Bernice Frederick HTL (ASCP)
Senior Research Tech
Pathology Core Facility
ECOGPCO-RL
Robert. H. Lurie Cancer Center
Northwestern University
710 N Fairbanks Court
I personally found the discussions on certification enlightening and
occasionally entertaining.
The opinions expressed are simply opinions - I do not judge them as nasty or
tedious.
If I am not interested in a discussion thread, I simply do not read it.
tg
-Original Message-
Join The National Society for Histotechnology in Orlando, FL this August for a
One-Day Forum on Troubleshooting Stains! NSH has recruited two of its highest
rated speakers to bring you this one day forum where attendees will learn good
practices for both HE and IHC Staining. The morning
We got an A+ rating.
Bernice Frederick HTL (ASCP)
Senior Research Tech
Pathology Core Facility
ECOGPCO-RL
Robert. H. Lurie Cancer Center
Northwestern University
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
b-freder...@northwestern.edu
-Original Message-
From:
Congratulations!!
WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC 29406
843-847-4586
843-847-4296 fax
This email and any files transmitted with it may contain PRIVILEGED or
CONFIDENTIAL information and may be read or
Hi Histonetters!
I hope you area having a great Friday and looking forward to a fun filled
weekend. I have a new position that I want to tell you about. I am working
with a lab in eastern TN that is setting up a brand new histology lab! This
is a permanent full time day shift position and my
I realize that this is a controversial topic, bu t I'm looking for a
definitive answer to the question of who can perfrom IHC and ISH in
Florida. I ask this because, in addition to attempting to comply with the
Federal CLIA regs governing labs, Florida has personnel licensure regs that
cover our
Hello Histonetters,
We are looking for someone who have a lot of experience in writing SOP
policies for Histology IHC (ie.CAP check-list). You can do them at
home (if your retiree) or in our lab. We will pay your service.
If you know someone who might be interested please tell them to
contact
Does anyone have a method/protocol for Pinkus’acid orcein-giemsa stain?
Thanks and good weekend to all
Luis Chiriboga
Experimental Pathology Core Laboratory
New York University School of Medicine
___
Histonet mailing list
Reagents:
Sol.A = water 30mL + 95%EthOL 70mL + HCl 0.6mL + orcein 1 g
Sol.B = HCl 0.3mL + absolute EthOL 97mL
Sol.C = Giemsa solution (0.05% eosin + 0.8% azur 5) 0.6mL + water 100mL
Sol.D = 0.001% eosin Y in 95%EthOL
Method:
sections → 70%EthOL → A x ½ to 1 hour → rinse → 95% EthOL a few dips →
I am presently writing a job description for the above position. Does anyone
have such a person in their lab? Could you share with me their job
description/salary range, etc.
Thanks
Nita
Nita Searcy, HT/HTL (ASCP)
Scott and White Hospital
Division Manager, Anatomic Pathology
2401 S. 31st.
Does anyone know a retic stain that does NOT use uranyl nitrate?
Individuals who have received this information in error or are not authorized
to receive it must promptly return or dispose of the information and notify the
sender. Those individuals are hereby notified that they are strictly
18 matches
Mail list logo