Hi,
how the FISH signals in FFPE tissue can be strenghten? by standard procedure
only weak signals for EGFR can be obtained, so far I tried different time in
Vysis protease 1 (45, 60, 70 min), for other probes 70 min works quite well on
our FFPE, but not for EGFR? what other modifications can
Hi,I wonder what is the way of removing shavings/trimmings from the cryostat in
other lab?, with the wet paper? gauze?, household vacuum cleaner - yes I saw
this in one lab!?thanksIrena
___
Histonet mailing l
we prefer filtration of urines through 5 mikron policarbonate filters
Irena Kirbis
Ljubljana, Slovenia
> To: bryan.wat...@neiurology.com
> From: dkb...@chs.net
> Date: Tue, 25 Oct 2011 09:46:06 -0400
> Subject: Re: [Histonet] Urine cytologies
> CC: histonet@lists.utsouthwestern.edu;
> histonet-
we made a cell block from cell line by following procedure:
- centrifuge cell suspension
- fix the sediment overnight in formalin (for tissue fixation) - optional, the
button will be anyway fixed by subsequent procedure
- centrifuge and decant the formalin
- add few drops of liquid agar (not too
Hi,
we have Arraymold more than a year now and we prepared around 10 TM's with it,
it is really simple, easy and effective, however
we found instructions to keep contructed TM overnight on 37 degrees uneffective
since recipient and donor paraffin were not blend enough, we keep our TM's
overnigh
Dear all,
could anyone out there provide a scientific reason for wearing gloves handling
slides with FFPE sections and FIXED cytology slides? I could understand that by
wearing gloves we could prevent epithelial contamination of cytology slides but
I would like to know which microorganism could
Greetings to all,
so far we handled wet-fixed cytology slides as health risk free without gloves,
however there is no data regarding this on the net (or at least I wasn't able
to find it). I would appreciate response on safety policy in other cytology
labs regarding fixed cytology slides and/or
I guess that you're staining these fix slides by Papanicolaou?, perhaps the
smears are too thick?,
we process daily different kind of smears and always prepare one fix and one
air dry smear for Pap and Giemsa staining and occasionaly we have an issue only
very muccous samples which can coming
so far we have good experiencies with it, it's very easy to use eg. it's easy
to prepare and construct TM, however we still struggle how to handle prepared
TM in order to keep all punches on the cut sections, it seems that this part
request some additional adjustment - at what temperature and h
how to prevent spots coming off during sectioning TM's? we do sometimes facing
problems sectioning TM's, they're just falling apart?
thanks for any hints
Irena
> From: hfe...@jhmi.edu
> To: sette...@umdnj.edu; ahut...@dh.org; histonet@lists.utsouthwestern.edu
> Date: Tue, 21 Dec 2010 16:13:31 -
I would recommend methanol or ethanol for fixation, smears itself can be
culprit of inconsistent staining
Irena
> To: histonet@lists.utsouthwestern.edu
> From: heather.mcl...@webmail.co.za
> Date: Wed, 24 Nov 2010 19:42:51 +0200
> Subject: [Histonet] carnoys fluid
>
> Dear Histonetters,
>
> We
for removing erythrocytes from hemorrhagic cytology samples we use filtration
of bloody suspension through membrane filter with pore size 20 mikrons, you can
find an article in Cytopathology. 2007 Jun;18(3):175-9. Epub 2007 Mar 27.
it is worth trying!
regards
Irena
> From: tmcne...@lmhealth.o
there are different slide preparation techiques used in cytology labs -
ThinPrep methodology, cytocentrifugation, membrane filtration are the most
often used, technique depends on pathologists preferencies and equipment and
experiencies of the lab!
hope this helps
Irena
> From: sjkit...@live.
Dear Valerie,
I can only agree that Papanicolaou stain is very tricky, having 20 yrs
experiencies with it! looks very simple but you need to know some basic rules.
first of all the slides should be hydrated at the beginning of staining
procedure since the hematoxylin is water based stain!
it se
14 matches
Mail list logo