Here ya go
caren.mie...@dako.com
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Drew
Meyer
Sent: Tuesday, February 09, 2010 13:22
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Dako Rep
Does
Hello Histonetters
We are having trouble with light staining from the hematoxylin. It is the same
lot number we have been in. We changed it out and still the same. All reagent
containers were emptied, cleaned and refilled yesterday. We have not changed
anything with the timings on our
Do you use city water in your wash stations? Have you had more snow/ice
than usual? If so the Water Tx Plant is putting more chlorine in the
water than usual. This will affect you HE.
Debbie M. Boyd, HT(ASCP) l Chief Histologist l Southside Regional Medical
Center I
200 Medical Park
Check pH of your washing water.
pH too low will result in not staining at all.
I'd clean the stainer as well.
Hello Histonetters
We are having trouble with light staining from the hematoxylin. It is the
same lot number we have been in. We changed it out and still the same. All
reagent
I am having trouble cutting FFPE liver sections. I have embedded the tissue
manually going from fomalin to water to increasing ethanol to xylene and to
paraffin. I can get good sections by soaking the block with ice cold water
before taking a few sections but then have to re-soak in order to
Hello to all in histoland. I had to come out of the box for this
question. What types of criteria do you have for verbal and written
counseling, as pertaining to histology functions. Any help in this will
be helpful.
Allison Scott HT(ASCP)
Histology Supervisor
LBJ Hospital
Houston, Texas
The criteria is simple = whenever what is described in the Competencies or
Standards of Performance is not met by the histotech.
1 verbal → 2nd verbal → written counseling.
René J.
--- On Tue, 2/9/10, Scott, Allison D allison_sc...@hchd.tmc.edu wrote:
From: Scott, Allison D
Hi everyone,
We have been trying to section gills lately and have come across
quite a few problems. Does anybody have any helpful hints for
fixing/sectioning gills? We are going to try to separate each
individual arch but the fish we use are very small so we don't know
how that will go.
If with small you refer to juvenile is different to an small adult. Both
will have supporting material for the gill arches but in juveniles they
should be easy to section after a good infiltration and using an adequate
paraffin wax to meet the tissue resistance.
If you are talking about a small
Question, when doing a smear for crystal indentification (Gout) are you
retaining the slide and for how long. How are you preserving it?
Thank
raj
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I would have a look at the haematoxylin stained section before you
differentiate.
Does it look OK? If it does then do not differentiate, blue only. (also
someone has not accidently put acid in the blueing solution? Check with
apH papers). You might try extending the Hx time.
If it still looks
Hey gang:
Here with some good news for once. I found out today that we WON our appeal to
JCAHO over our tissue retaining time. They are giving Mohs labs an OK not to
have to retain our tissue!! I guess it is 'processed' tissue instead of 'gross'
tissue. Retaining it doesn't does not help
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