Hello every body,
First I would like to thank you all for your great feedbacks and attention
which is such a big improvement in my work, Thank you all!
Then, I was wonder if any one has experience on this tissue: rat hind paw skin
( which is hairless).
Any inputs will be appreciated, whether
Our laboratories are currently working on policies to address specimen
identification/labeling errors. This is to be a laboratory policy and will
include pathology. Would anyone be willing to share policies that they have
that address this and any punitive action that is mentioned? I know
If anyone wants to cut down on cutting injuries. Teach the new techs to
use two forceps instead of your fingers. I'm too old to change but I
know a tech who cuts this way and has never had an injury. It works
really well on automated microtomes. Anne
-Original Message-
From:
Has anyone tried to embed cells grown in tissue culture? I am trying to put
some tissue culture cells through same stress as tissue would go through.
Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and then
fix for extended time with NBF but that doesn't quite seem fair.
Making cell tissue blocks
Cells:
. Harvest and fix in formalin* for at least 3hrs or overnight (10 fold
more formalin)
. HAVE A NICE VISIBLE SIZE PELLET (1 confluent T75 minimum or 1 T175)
. Remove formalin* and wash 2x's in cold 1x PBS
. Cover cells with some 1x PBS and
Hi all... sending out for a colleague...
After implementing the Vantage system, a lot of their ISH slides have a
purplish to bluish haze on the slides. Not all of them, but some and it seems
to be consistent. No problems before Vantage. They were using the longer
labels from Ventana for
Karen,
We experienced a similar problem with the ISHs at our laboratory a few months
ago with the Kappa, Lambda, Eber and HPV. Our pathologists were complaining of
a blue crystal-like precipitate on all ISH slides.
Our Ventana Technical Specialist recommended that we try the NO ALCOHOL
I spun down the cultured cells and then used a product called histogel. It kept
them protected through the VIP, paraffin embedded like cell block buttons and
was able to cut regular paraffin sections. I believe that I purchased the
histogel from American Mastertech.
Joelle Weaver MAOM, HTL
Mike,
For EM work we fix, scrape the plate into a microtube, centrifuge at 1800 rpm
for 10 min and then embed in Histogel or agar. Processing after that is as
usual. They look fine by EM. I'm sure they would look fine by paraffin
processing as well.
Tim Morken
Supervisor, Electron Microscopy
Dear Histo Folks,
I am in the process of setting up a brand new histology/IHC laboratory on the
campus of the Uganda Cancer Institute in Kampala, Uganda in conjunction with
the Fred Hutchinson Cancer Research Center. As you can imagine, we need
anything and everything as supplies and small
Thanks for all the great replies!! While I have you all worried about my cell
pellets ;-) Does anyone have a good anti-HuCD20 that works well for FFPE
tissues (cells).
Thanks!
Mike
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Congratulations Sarah
Sincerely,
Toysha N. Mayer, MBA, HT(ASCP)
tnma...@mdanderson.org
Instructor/Education Coordinator
Program in Histotechnology
School of Health Professions
MD Anderson Cancer Center
713-563.3481
Message: 1
Date: Wed, 27 Nov 2013 19:13:05 +
From: Sarah Dysart
I'm currently designing a new GI lab. Any advice on grossing stations? The
only name I know is Mopec. Is that the best one to go with or are there better
ones out there? Thanks!
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I think that's the best - you can charge for rides - up and down!!
Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org
www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA 30342
This e-mail, including any attachments is the
http://www.thermoscientific.com/en/products/pathology-work-stations.html
Douglas A. Porter, HT (ASCP)
Grossing Technician
IT Coordinator
Cancer Registrar
CAP-Lab, PLC
2508 South Cedar Street
Lansing, MI 48910-3138
517-372-5520 (phone)
517-372-5540 (fax)
In which animals works also this antibody ?
Thanks
On Mon, Dec 2, 2013 at 11:20 PM, Jan Shivers shive...@umn.edu wrote:
Dako's MAC 387 (cat. #: M0747)
On Mon, Dec 2, 2013 at 2:09 PM, Jackie Ferracone
ferra...@vet.upenn.eduwrote:
Hi All,
Looking for good macrophage markers for equine
Sad news. I received an email over the weekend from a histotech, that Chris van
der Loos died on Nov. 26, 2013. I was able to talk with the NSH office today,
and got it confirmed. There is information about Chris on the NSH webpage as of
later this morning.
I've had it to work in cat, cow, dog, fox, horse, otter, pig, and raccoon
in my lab.
According to vendor - it's supposed to also work in guinea pig, monkey,
rabbit, and rat, but I have not tried it in those animals
Needs either enzyme digestion or heat antigen retrieval.
Best regards,
Jan
Very sad news indeed. He will be missed dearly!
Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
2855 Gazelle Ct.
Carlsbad, CA 92010
760-603-2371
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
This is very sad.
Chris was knowledgeable, with a wonderful sense of humour and always had time
for his colleagues.
He will be missed
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager Senior Scientist, the Children's Hospital at Westmead
Adjunct
I had the privilege and good fortune of getting to know and swap ideas with
Chris after spending a few weeks with him in Breda back in 2001.
Never short of advice and always willing to help and learn from others.
To use an Australian expression he was an absolute Cracker of a guy.
Cheers
Jim
I agree
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager Senior Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney
Tel: 612 9845 3306
Fax: 612 9845 3318
Pathology Department
the
Hi Leila
As no one seems to have responded to your email I will add a few items.
I used to do some work on wound healing on mouse footpads so circumstances
are the same.
If you are looking for melanin routine fixation and processing should be
finem, melanin will remain.
Only thing is that the
Hi,
There are a few ways of doing this. Perhaps the easiest is scraping the
cells off while it is still in the media. Transfer it to a centrifuge tube and
spin it down. Pour off the supernatant add formalism vortex it and centrifuge
it again and pour off the supernatant again and add
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