Hello everyone, I want to introduce myself to all the histotechs here. I
have visited this forum before but I finally subscribed today. My name is
Valerie, but please call me Val. I am an histotechnologist living in Puerto
Rico. I got interested in the field of histology in 2008. I always loved
The new derm path lab I am associated with built their own computerized
specimen tracking system and I am pretty sure that the same multi unique
identifiers that are printed on the slides are printed on the blocks. They
have leica slide and block printers connected to accessioning and grossing
by
Is the Perma Red for hrp? If you switch to an alk.phos detection system you
could use fast red which is much redder than AEC. Dako sells ap/red
detection systems, but I prefer to use Vector Red for AP.
Patsy
Patsy Ruegg, HT(ASCP)QIHC
IHCtech
12635 Montview Blvd. Ste.215
Aurora, CO 80045
Morning All,
My chief pathologist has asked the following question. For all of those
doing Her-2 Neu staining for scoring with the Vias system. How many control
slides do you cut in advance and how long are they viable if kept
refrigerated?
Thanks in advance,
Rae Ann Staskiewicz
dear Val, first my english is not good. I can understandbut the grammar!
My way is similar- after studies I wanted to work in microbiologie.
But I´ve got a job in Pathologie. First time I was alone in the
laboratorie.I had to manage the routine...cutting,staining,preparation
and so
I have to imagine that you are doing the HIER in the FFPE sections? If you have
used autoclave unsuccessfully it seems that the epitopes are so cross-linked
that they do not respond to the treatment.
I would try a piece of fixed tissue before processing, cut it in a very thin
slice (about 2 mm
Hey there. I have done IHC on mouse placentae that have been fixed in NBF for
over 2 years and it took me 5-10 minutes of ProK (10 ug/ml in PBS) followed by
60 minutes of HIER in 10 mM citrate buffer (made sure PBS was at pH 6) in a
veggie steamer.
I had previously done this IHC in a
I have routinely seen that we obtain slightly different results (like 10-20%
variance) in using 35S dATP for TdT-catalyzed tailing reactions of
oligonucleotides from month to month as we use different batches (made fresh
monthly) of the 35S dATP. But on a few occasions over the years we have