Is anyone out there doing the PGP 9.5 on fresh or frozen tissue?
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I will be out of the office starting 07/08/2010 and will not return until
07/09/2010.
I am out of the office for the rest of today. I will reply tomorrow,
Friday, July 9th.
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Hi,
I am detecting Arc (Activity regulated cytoskeletal protein) protein in rat
brain slices.
I perfuse transcardially the animal with 0.1M PBS and than 4% PFA with 5%
sucrose. Post fixation in 30% sucrose 1% PFA. In some cases when i take out
the brain after the perfusion i make small cut or inc
I am looking for a condenser cooling fan motor for my Histo -Bath. Thank you
for any Help .
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We are currently looking at a overall computer system for our Hospital. My
point of this question is has anyone worked with and their feelings about the
following vendors for the AP application:
Meditech
Cerner
Quadra Med
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I you are going to choose to override the prompts, you had best revert
back to a schedule of changing solutions on a rotating schedule.
You probably had something like that in place with your previous
processor. I would call Leica to have them send out someone to help get
your processing optimiz
I have been asked about bringing this antibody in house and I was
wondering if anyone is staining for this using a Leica Bond stainer.
Any advice, tips, etc. would be appreciated. We are looking at getting
the antibody from Dako, cat# Z 5116. Thanks in advance for your help.
Martha Ward, MT (AS
The machine will work well only if it is set up well and the staff follows
all of the prompts. We set up ours with two stations of 80% alcohol in the
beginning to make sure it starts with a good graded series of alcohols.
Another thing to look at is the biopsy pad percentage. Setting it right
wil
We have helped that problem by being sure there is adequate graded
alcohols on the Peloris. There must be between 60-70%, 80-90%, and 95%
before you have the 100% alcohols. If the concentration's are too high
there is inadequate infiltration of the tissue's. We usually only use
the 2 hour and
To all you Peloris users, here is my delimma. When we follow the machines
prompt to change the solutions because of purity and we then process small
biopsies on the machine, it overprocesses the specimens. So the staff have been
overrriding the prompt to change the solutions causing specimens t
What Tony suggests is similar to what we do for reprocessing. If we have a
block that we embedded and attempted to section, only to discover that it's
not fixed well enough, we do the following:
1) print a new processing cassette
2) using a "dull" knife (we have an old, dull steak knife), run the
Having switched from an HSV I & II antibody cocktail to separate
antibodies for HSV I and HSV II, we have found (and the manufacturer has
confirmed) that the two separate antibodies cross react. Does anyone
know of antibodies against HSV I and HSV II that do not cross react?
Thanks,
Linda A. S
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