Hello again my fellow histonetters, I was hoping someone could give me their
thoughts on this issue:
We receive Derm biopsy specimens in formalin containers. We gross the specimen
and place the cassettes with the tissue in it in a tray with 10% formalin.
Although we have grossing tables with ex
Hello
I am writing to request if you could send me the protocol of
Inmunohistochemical staining for reduce the Paraffin fluorescence. I saw
that the people use evans blue, but I don´t know how can I do?
Thank you
Good weekend
ALDANA VISTAROP
Laboratorio Biologia Molecular, Servicio de
I have used a keyboard at embedding, but no mouse. The other tracking uses I
have seen use scanning of bar codes or QR codes not keyboard or mouse entry.
Joelle Weaver MAOM, HTL (ASCP) QIHC
> From: donna.wil...@baylorhealth.edu
> To: histonet@lists.utsouthwestern.edu
> Date: Thu
Thank you Tom and Pat-
Here are the biopsy sizes:
I have my classes experimenting with specimen size to try to find what will
work best for our situation. My 1st block class has 2mm biopsy cores, 2nd
block has 4mm biopsy cores and 3rd block has 6mm biopsy cores- each about 2- 3
mm thick.
I w
Hi Adelle, Biopsy sizes will matter, but you might shorten some of these times,
but be sure to add at least one more Histoclear to make sure there is no
alcohol in it and at least one more paraffin to make sure there is no
histoclear carryover.If you go back to 70% at any time you will have to s
First of all THANK YOU for getting our field into a high school and teaching
the kids. This is a very good thing for all of us in the field.
Could you give us an idea of the size of the specimen you are attempting to
process? A great deal depends on the tissue size as to how long it can be l
Hello everyone,
I have been following and learning from this listserv for the past two years, I
have enjoyed all of the advice this forum presents. This is my first inquiry
for the group. I am a high school Anatomy and Physiology teacher and a grad
student at Thomas Jefferson (Philadelphia, PA
Our tracking system has everything there. We can create templates for various
scenarios based on what is needed. The barcodes are generated by the system.
It's a complicated system and takes a little time for data entry and such, but
it does work. Our microscopy area is not set up in it as of ye
Anyone know how to troubleshoot this Retic issue? The stain result is not
the usual continuous silver stain reticulin fibers. Instead the fibers are
more like dashed lines and the fibers are not visible throughout the entire
tissue, especially edges. Ventana benchmark machines being used with thei
