(2nd attempt)?
To all:
I have a Neuro-Pathologist colleague that is looking to learn how to use a
sliding microtome. Is there anyone out there that would be willing to show him
the basics?
Walter Benton HT(ASCP)QIHC
Lab Operations Manager
Chesapeake Urology Associates
806 Landmark Drive,
Dear Histonet,
My name is Mari Yang and I am a doctorate student pursuing a degree in
Management and Organizational Leadership. I have the unique opportunity
to facilitate a study exploring the extent to which spiritual leadership
positively influences organizational commitment, productivity,
To embed the tissues with paraffin you HAVE TO dehydrate the tissue. This is
usually done with either ethanol of 2-propanol but essentially all dehydrants
will remove fat so you are right, the way to go is going frozen sections.René
On Thursday, March 24, 2016 2:24 PM, "Dessasau III, Evan
Hi Histonet, is there a way to process tissue for paraffin embedding without
using alcohol? One of the labs that send their
processing to us will be doing a study examining fat. I told them if they
want to look at the fat they will have to cut frozen sections but I'm
I would not recommend florescent pink, red or aqua. The colors that we
currently use are yellow, white, green, lilac, light pink (salmon), and orange
(on Printmate's only). We had many trials and tribulations when it came to the
barcodes actually scanning. We went through three different
Good morning everyone!
Do any of you have any advice regarding which color cassettes do not work well
with the barcode scanning systems currently in use today?
Thanks much!
Jeanine H. Sanders
Infectious Diseases Pathology Branch
Centers for Disease Control and Prevention
1600 Clifton Rd., NE
http://www.chicagonow.com/downsize-maybe/2016/03/never-let-a-doctor-plan-your-lunch/
Lester J. Raff, MD MBA
UroPartners
Medical Director Of Laboratory
2225 Enterprise Dr. Suite 2511
Westchester, Il 60154
Tel: 708-486-0076
Fax: 708-492-0203
___
Histonet
We use the syringe used for the smears and the syringe used for the aspirate.
We do not put it in an anti-coagulate. We simply let the syringe specimen clot
and place it in lens paper in a cassette and place in 10% formalin for
processing. If you are doing Flow Cytometry/Cytogenetic studies