Hi guys,
I am wondering if anyone has much experience storing slides in buffer
(PBS-T) after retrieval for up to about 48hrs at 4C? Is it likely that they
will still stain? Or is it going to be entirely dependent on the epitope?
I'm optimizing research antibodies right now and I'd like to
Hi,
Do you know a way to stain damaged mitochondria in rat hearts after
ischemia/reperfusion by immunohistochemistry?
Thank you very much!
Felix
--
Felix Nagel
Ludwig Boltzmann Cluster for Cardiovascular Research
c/o Core Unit for Biomedical Research
Waehringer Guertel 18-20 - Leitstelle
Are you soaking your blocks in dilute ammonium hydroxide before sectioning?
Soaking too long will affect stain quality.
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902)
Glawon,
Thank you for your help. I appreciate it.
Betsy
-Original Message-
From: Glawon Flood [mailto:smoo...@gmail.com]
Sent: Tuesday, March 15, 2011 2:33 PM
To: Molinari, Betsy
Subject: Re: [Histonet] Bielschowskys Stain
Betsy,
I don't know of any modifications for Eager's but there
I just did this last week. I stored them in wash buffer overnight in
the frig. and they were fine =)
Sarah Goebel, BA, HT(ASCP)
Histotechnologist
Mirna Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas 78744
(512)901-0900 ext. 6912
-Original Message-
From:
Hello everyone,
I have an issue that I would like some help with. We are currently running
SMM-HC and E-Cad on Breast cores and specimens from a derm lab. With the
regulations being so strict regarding the processing times of breast
specimens, how are you all dealing with that when it comes
Hello out there in Histoland,
I'm looking for a procedure for making your own Gram controls. Any
assistance would be appreciated.
Thanks, Randi
/pre--- Horizon Health Network Disclaimer ---brbrThis e-mail
communication (including any or all attachments) is intendedbronly for the
use
Making you own...not sure how to do that, but Slim Jim's work in a pinch.
Walter Benton HT(ASCP)QIHC
Histology Supervisor
Chesapeake Urology Associates
806 Landmark Drive, Suite 126
(All Deliveries to Suite 127)
Glen Burnie, MD 21061
443-471-5850 (Direct)
410-768-5961 (Lab)
410-768-5965 (Fax)
Hey all,
There is a PRN position at Longmont United Hospital open. Working Mon-friday no
weekends no evenings.
I have attached the link to apply.
http://longmontunitedhospital.force.com/Careers/ts2__JobDetails?jobId=a0IA002ct4yMAAtSource=
thanks
Matt Lunetta HT(ASCP)
Longmont United Hospital
It makes sense that some epitopes might be more sensitive than others. For
48 hours, I would probably store in just PBS, and leave out the detergent
(I am assuming the 'T' in your PBST is Tween). Even though Tween is a weak
detergent, I would worry that long-term detergent treatment might dissolve
Randi,
I don't have a written procedure to forward to you, but this is what we do when
we make our gram controls. We use fresh tissue from an autopsy before it goes
in formalin (such as lung, we've used placenta before as well). Then put a
couple pieces of the fresh lung into containers
I'm looking for a mouse anti human S100 A1 antibody for IHC.
My vendor doesn't carry it anymore.
Anyone have one that they are using on FFPE tissue?
Could you send me ordering info or a copy of your data sheet?
Thanks,
Angie
Angela Bitting, HT(ASCP), QIHC
Technical Specialist, Histology
We seem to be constantly battling this as well. We have found that the quality
of the ethanol used in processing and staining can be an issue. We now purchase
ours from a company at www.UltraPure.com. The quality of the DI or distilled
water being used can also be an issue. We are currently in
Regarding CAP checklist, question ANP.23041. The operation of the imaging
system is performed by high-complexity testing personnel.
We have a question regarding the qualifications of the operators. The
operators of the Aperio system are simply scanning entire slides to make a
record for
For 10 years I ran Histology lab for a large University. We used the same
equipment and lab for both animal and human tissue.
I had to certify the lab with CLEA for human tissue at one point (and this
took serious work!). If you are already certified for human, using the more
strict regulations
Mark this is a new question and let me answer this for you from a
inspection point of view. Currently there are 15 to 18 new questions
that deal with predicative markers and the digital images, most of these
are QA/QC related. But the issue with images is that your people are
inspecting them.
Well I wouldn't try and use a Ph.D. in religous studies to qualify for high
complexity testing...
On Wed, Mar 16, 2011 at 4:36 PM, Mark Turner mtur...@csilaboratories.comwrote:
Regarding CAP checklist, question ANP.23041. The operation of the imaging
system is performed by high-complexity
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