Hello,
I am here again. I am wondering if someone has good experience
embedding in gelatin-albumin for cryostat or vibratome sectioning.
Specifically we use brain tissue and is common in free floating techniques
non-attached parts of the same section float around and later that
generates all
I don not know any method for tattoo pigment removal. Aside from carbon black,
most of the red, yellow, blue and green pigments are metal salts and polarize
brightly. The inflammatory response may be vigorous, especially w repeat or
Re-do of a tattoo. In some cases a pseudo-carcinoma or KA
Hi:
I teach college human anatomy and physiology and would like to have a slide
or two of human skin with tattoos in cross section. Do you know where may I
get a hold of those? All I use these days is an illustration from the web.
Please, email me directly if you have constructive suggestion.
Hi everyone,
We are a smaller hospital that stores our blocks, slides and files off site
with a 3rd party storage facility. Does anyone have any information on fees
for storage of blocks, slides, records and how much they charge to pick-up and
deliver when needed and the names of any
Hi Histonetters!
Here is my latest blog post on the NSH - Fixation on Histology site:
"Strategies for Coping with the Shortage of Histotechs.
TGIF. Have a wonderful weekend!
Thanks-Pam
From: Fixation on Histology [mailto:hi...@nsh.org]
Sent: Friday, January 17, 2020 1:07 PM
To:
The only way I know of is through lasers
On Fri, Jan 17, 2020 at 12:25 PM John Garratt via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> It is a pigment (ie carbon) and not like a soluble ink, so good luck with
> that.
> You could consult your histotech text book on exogenous pigment
It is a pigment (ie carbon) and not like a soluble ink, so good luck with that.
You could consult your histotech text book on exogenous pigment removal and
give the recipe a go. I will certainly be interested in other histonet replies.
John
www.cpqa.ca
‐‐‐ Original Message ‐‐‐
On
Hello fellow histonetters,
We received a skin sample that has ink from a tattoo - the sample if from
tattooed skin. One of our pathologists would like us to see if we can get
rid of the tattoo ink from the sections before H staining. Does anyone
out there know how to do this?
Thank you,
Donna
Standard protocol for replacing microtome blades anybody have this or can help??
Thanks
S Kathy Baldwin ASCP, SCT
Memorial Hospital and Health Care Center
Pathology and Cytology Manager
Ph 812-996-0210
Fax 812-996-0232
CONFIDENTIALITY NOTICE: This e-mail message, including any attachments, is
Good Morning,
We have recently opened a new Histotechnologist position with WVU Medicine!
This position is eligible for a generous sign-on bonus, full comprehensive
benefit package, and a competitive salary range. I invite you to contact me
with any questions about this exciting
Some predictive text issues like lyse and nucleated.
Sent from my iPhone
> On 17 Jan 2020, at 8:24 am, Tony Henwood (SCHN) via Histonet
> wrote:
>
> Hi Jennifer,
>
> I have had excellent success with lysing the red blood cells (using Isotonic
> Ammonium Chloride) prior to cell block
Hi Charles
A method my EM scientist used many years ago was quite simplistic and he
thought it worked well.
You simply centrifuge the specimen, add a set volume of deionised water, mix
to lose the red cells, then add an equal volume of double strength normal
saline to create a suspension in
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