Hi César
we use mo-a-C4d, clone CL314 (Quidel A213) at 1.25 ug/ml (1:800) for
cryosections of kidney biopsies (indirect immunofluorescence), it won't work
on FFPE material (at least in our hands). For FFPE, Biomedica's rb-a-C4d
(BI-RC4D) works fine at ca. 6 ug/ml (1:30) after HIER in a high pH
Hi all,
I am lookin for a substitute for Technovit 7100 in our research (currently
on fish female gonad). Any help or suggestions about this point would be
very very appreciated.
Best regards
Jorge Tornero
IEO - Cádiz- Spain
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We get our from Alpco.
Angela Bitting, HT(ASCP)
Technical Specialist, Histology
Geisinger Medical Center
100 N Academy Ave. MC 23-00
Danville, PA 17822
phone 570-214-9634
fax 570-271-5916
No trees were hurt in the sending of this email
However many electrons were severly inconvienienced!
Hi Histonetters!
I hope everyone is having a great day. I have a new opportunity I want
to tell you about!
I am working with a brand new specialty lab opening in the Poughkeepsie
area. They are in need of 2 histotechs 1-junior and 1 senior tech.
for full time permanent day shift positions. The
Hello All,
How long is hematoxylin (we use Richard-Allen Heme 2) good for after it is
poured into a staining container? The stain gets used so infrequently I would
like to keep it as long as I can. We currently dump it weekly regardless of
use. Thank you.
-Kristen
Our's is from Zytomed, a polyclonal rabbit (a12-5000). We work with the
benchmark XT, 1:25 with amplifier.
Gudrun
-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von Cesar
Francisco Romero
Gesendet:
Hi All I just wanted to say thanks to everyone who has responded to my question
regarding formalin waste going down the drain. I appreciate it!
Have a great day!
Jessica Piche-Grocki, HT(ASCP)
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What I do Kristen if I use it infrequently is I get a large brown bottle, label
it with working hematoxylin. After I use the hematoxylin for whatever I am
using it for I pour it in the brown bottle, cap it tightly and store it on the
shelf or in a cabinet. Whenever I need it again I get it
Hi everyone,
When carrying out IF on frozen sections how long after the cutting the sections
should you leave the slides to dry and where before starting the staining
procedure?
Thanks a mill,
V
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We don't let our unfixed sections air-dry (room temp) long before fixing
them - a few minutes? For some people here I let them sit a few minutes
then just store them in the -80 for up to a weeks weeks before they fix
them and commence with their staining procedure. If the animals were
sorry, that should read for up to a few weeks.
--On Tuesday, March 24, 2009 1:00 PM -0400 Merced Leiker
lei...@buffalo.edu wrote:
We don't let our unfixed sections air-dry (room temp) long before fixing
them - a few minutes? For some people here I let them sit a few minutes
then just store
Vanessa,
The answer of how long is suitable, the answer is it depends.
Routinely, many will air dry over night, even over a fan, in order to achieve
the best adherence to the glass slide. We have found that we lose
immunoreactivity with some antigens if we let it go that long. Our routine has
Hi, does anyone know of a reference or service lab that does immuno staining
for PDGFR-a,b (platelet derived growth factor receptor alpha and/or beta.
Please note my new street address and phone number
Tim Morken
Technical Support Manager
Immunohistochemistry
Anatomical Pathology
Thermo
USLabs performs this test.
Jaime
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken,
Tim
Sent: Tuesday, March 24, 2009 10:39 AM
To: histonet
Subject: [Histonet] Reference or service lab that does
Does anyone know of a method to change the pH of tap water without going
through a lot of expense? Possibly a filter to put directly on the water line.
Thanks,
Toni
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]on
I was wondering if there are any clinical labs that use the LabVision line
of instrumentation, antibodies and reagents.
We are a small hospital that does about 30 predilute antibodies and are
considering changing from our current vendor/instrument.
I would appreciate good, bad experiences. I
We do 3 to 4 FNA's on a daily basis and no matter the site thyroid, liver ..Etc
we go through the time out procedure every time, yes it may a little bit
overkill for a palpable mass or using ultrasound guidance but none the less you
must do it just like labeling the lido cane when it is the
I'd go for the old AO 820. They can be used by any and everyone and its
nearly impossible to break them.
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Lynn Burton
Lab Assoc. I
Animal Disease Lab
Galesburg, Il 61401
From: Burton, Lynn
Sent: Tue 3/24/2009 10:31 AM
To: histonet-bou...@lists.utsouthwestern.edu
Subject: formalin neutralizers
What is everyone using to neutral their formalin? Who has the best
Hi Rene,
I love LabVision products! Hopefully they won't be ruined by Fisher(I
would put in names of all acquisitions but it would take too long to type)...
Noelle (LabVision cheerleader)
Noёlle Linke M.S., HTL(ASCP)QIHC
Manager, Histology Services
Department of Pathology Laboratory
Hi,
Has someone tried an antibody that would detect CD31 on mouse tissues
using 10% NBF and not Zinc formalin?
Thanks,
Lizbeth Kelly, HT(ASCP), Q-IHC
Histology Department
Human Genome Sciences, Inc.
14200 Shady Grove Road
Rockville, MD 20850
240-314-4400 X2325
Fax: 301-354-4176
30 min at room temperature
René J.
--- On Tue, 3/24/09, Vanessa J. Phelan vjp2...@columbia.edu wrote:
From: Vanessa J. Phelan vjp2...@columbia.edu
Subject: [Histonet] IF
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date: Tuesday, March 24, 2009, 12:17 PM
Hi everyone,
The final program is available for the California Society for
Histotechnology annual symposium. The symposium is scheduled for May
14-17 in Millbrae.
If you are interested I can send you a word document or a pdf file. It
will be posted on the CSH website in the next day or so.
We use ours for a few weeks, but we do filter it before use.
kristen arvidson arvidsonkris...@yahoo.com
Sent by: histonet-boun...@lists.utsouthwestern.edu
03/24/2009 07:48 AM
Please respond to
arvidsonkris...@yahoo.com
To
histonet histonet@lists.utsouthwestern.edu
cc
Subject
[Histonet]
Hi, all
I have a question about how to QIHC certificate. We have several
bilogical scientists work as full-time employee doing IHC
staining. But none of them has HT certificate. In this case, can
they get QIHC certificate? What kind of courses need they to
take?
Thank you,
Ann Fu Lab
Hi all. Having a bit of an internal debate here, so I would like to get
the opinions of some of you in Histoland, please. Here are the
questions:
1.When fixing with 10% NBF, for how long should you fix and what
volume ratio of fixative:tissue should you use?
2. At what
1. Generally 24 hrs for 2-3 mm thick piece. At least a 10:1 formalin:tissue
volume.
2. Room temp or 4oC - I've heard debates, and I've heard it doesn't matter,
but we do it at 4oC.
--On Tuesday, March 24, 2009 4:54 PM -0400 Jacqui Detmar
det...@lunenfeld.ca wrote:
Hi all. Having a bit
Hello Histonetters,
Have a new project that wants to stain CD20 in mouse samples. One is
brain and the other heart. Has anyone done this CD marker in mouse? if
so, would you be willing to share with us!
Thanks in advance,
Colleen Forster
U of MN
Hello,
We do IF's on renal biopsies and skin. We were getting our antibodies
and Protein Block from ThermoShandon which is now Lab vision. We are
now not getting our supplies when needed. We have Protein Block on
order and were told we would not get any until end of April, which was
then
I am looking for help/advice for using our automated immunostainer the
Microm HMS 710i .(Our user manual says Richard Allan Sci and the labels on
the side say LabVision, we have calls into Thermo's LabVision department but
they are unsure if they can assist us)
Specifically, one of our problems
This is what we use:
Neutralization and Disposal of Formalin Fixative
10% Formalin can be neutralised with sodium bisulfite or concentrated ammonia.
The reaction with ammonia results in the formation of hexamethylenetetramine
(commonly known as hexamine or methenamine). This can then be safely
From the ASCP Board of Registry webpage:
www.ascp.org/bor
Click on Qualifications
Click on IHC
There are 3 routes. To summarize, all experience must be within the last 5
years, in a US lab, Canadian lab, or CAP/JC accredited lab:
1. ASCP certified technologist + 6 months full time IHC experience
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