I have always found there are so many variables that having an expectation of
setting a set number is not always possible. I feel they should be compared to
their own standards and not of their co-workers. If they can cut or embed a
set number on a particular than they should maintain or
As well we have used mushroom and other moldy food products but it only
demonstrates the mold and not tissue elements. But you can mince tissue and
mix it with the fungus or mold so it one big segment and this gave more
desirable results.
Diana
-Original Message-
From:
In the past when we receive these samples there has been no issues cutting
them. Over the past few months there has been a tendency for these blocks to
shred into fine strips when cut. Almost like there was sand in the blocks.
Mollifex, decal, warm or cold, doesn't matter they still shred.
Is anyone using this module and are you willing to share any documents
regarding it. Or opinions on what think of it for a QA program
Sincere thanks
Diana
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There was a recent post for someone inquiring about cryomolds. I have not used
these and have researched them and found out the Sakura cryostat has a cryobar
with recessed ports to accommodate these molds. Has anyone used these on a
Microm microtome. Is there a problem removing the molds and
I did not know such a product existed until now. How do these molds work?
Diana McCaig
Histology Lab
Chatham Kent Health Alliance
80 Grand Avenue West
Chatham. Ontario
N7L 1B7
519-352-6401 (6604)
This email communication and any files transmitted with it may contain
confidential
I sent out a request for information a while back and am going to ask again
from a different approach.
I am finding problems with embedding blocks of bone marrow particles with or
without blood clot.
Does anyone have a special technique they would like to share to concentrate
the particles
Can anyone share with me their process for processing bone marrow aspirations
and embedding them in paraffin blocks. Currently ours are being spread out
throughout the entire base mold and makes it cumbersome to screen. Has anyone
used histogel or making a button and embed that instead of
Does anyone have spare reagent containers for a VIP5 they are willing to sell.
I am looking for 3 to use exclusively for warm water wash. We are located in
Ontario, Canada
Diana
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I know this topic has been beaten to death in the past and do realize it is
dependent on tissue
orientation, quantity of pieces in a block, and experience.
There are guidelines suggested by the College of Med Lab of Ontario in a
document Oct 2008
that indicates the expected minimum daily range
What is the shelf life of prepared 1% Alcian blue in 3% Acetic Acid?
Diana
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Is anyone willing to share their staining protocol for Cresyl Violet stain for
HP
Thanks
Diana McCaig
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We are going to be setting up a Leica 6025 Processor. Can anyone send me their
SOP and worksheets that you have created so I can use them as a reference and
modify them according to our usage. Would truly be appreciated as well as any
helpful tips or tricks you have encountered.
Diana
Does decalcifying tissue (Calex II) affect the antibody reaction for IHC in
bony tissue?
Diana
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What stain are you using for HP?--Giemsa. Warthin Starry or IHC.
Do you do them routinely or only when requested?
Are they done on an autostainer or with a kit?
Diana
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Can you please give me your routine for processing breast cases over the
weekend. Do you extend the time in alcohol to achieve the 48 hour
maximum, call someone in over the weekend, or just indicate on the
patient report that the fixation extended beyond the 48 hours limit for
HER 2, 72 hours for
Can you tell me what thickness you cut your routine slides for HE and
immuno (in particular lymph nodes).
Also, your protocol for cutting prostate needle core biopsies.how
many spares you cut and do you designate the level on the slide label if
multiple levels are submitted on one slide?
I was hoping to get information on why special stains are dehydrated,
cleared and mounted vs allowing them to be blotted dry, air dried then
coverslip.
Every procedure I have ever encountered always indicates to dehydrate
and clear but I have heard where some labs are blotting the slides ,
Would this work for auto cover slipping (tape film)if they were set in the
xylene reservoir prior to cover slipping?
Diana
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of E. Wayne Johnson
Sent:
Can you please let me know what options for counterstain there are other
than Nuclear Fast Red or a supplier who sells the prepared solution
Diana
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We have no tissue in a block and would like to take the negative control
and stain it for synaptophysin. We are using the Nemesis, Biocare Mach
4, AP protocol.
Sincere thanks
Diana McCaig
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Is anyone willing to share with me their quality assurance/management
program for pathologists.
Sincere thanks
Diana
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Hi
Does anyone using PowerPath have a turn around time report?
Diana McCaig
Histology Lab
Chatham Kent Health Alliance
80 Grand Avenue West
Chatham. Ontario
N7L 1B7
519-352-6401 (6604)
This email communication and any files transmitted with it may contain
confidential
Can you tell me how long you let your IHC slides air dry at room
temperature and how long you put them in the oven prior to staining?
Thanks
Diana
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We are trying to validate a Biocare decloaker and have found when we use
122 degrees for 30 seconds we get great signal, but distorted
morphology.
If we reduce to 90 degrees for 45 minutes, the signal is significantly
decreased but the morphology is good.
What protocols are you using?
We are using Biocare Smooth Muscle Myosin-Heavy Chains (AP Protocol
using Warp Red and previously Vulcan Fast Red)on the Nemesis auto
stainer.. Lately we have notice considerable background staining. Any
suggestions. The slides almost look like in the old days when you put
too much albumin ( as
Does anyone have a method for identifying uric acid crystals in gout on
a tissue sample.
Diana
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Does anyone have a procedure for a combination MTS/VG elastic stain that
they would be willing to share?
Diana
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I am looking to purchase diastase to use for the PAS/DIASTASE stain. I
see there are many options in the catalogues. What is recommended?
diana
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If you do a run of several immunos today and you run a negative control,
and there is a request for additional immunos tomorrow, would you run
another negative control with the additional slides. They are being
stained on a stainer and not manually,
diana
Does anyone run a HE control prior to staining a frozen section?
Diana
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Hi
We have been doing a PAS stain on the same control block and same
reagent supplier for a long time.
Yesterday when we ran the slides, they failed to stain
We opened new bottles of Periodic Acid and Schiff's Reagent and recut
fresh controls
Still, we are unable to get any staining.
Can someone provide me with a supplier of tissue marking dyes for use on
the grossing bench.
Diana McCaig
Histology Lab
Chatham Kent Health Alliance
80 Grand Avenue West
Chatham. Ontario
N7L 1B7
519-352-6401 (6604)
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Can anyone share with me their procedure for AB-PAS for Barrett's
Esophagus.
With thanks
Diana
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We have been notices folds and wrinkles in the needle cores biopsies
that do not seem to be affected by increased soaking. I am inclined to
think it has to with processing. Currently they are done with the
routine surgical specimens .What is the preferred schedule for needle
cores? Is it best to
I think there is confusion regarding the original question posed. They
were not asking about the HPS stain. Some hospitals use an
eosin/saffron stain in their routine HE. I had another lab recently
asking about the formula to prepare this solution instead of eosin. Any
advise?
Diana
Is there a minimum time for prostate biopsies to be fixed. Does
fixation times affect PIN4's?
Diana
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Can anyone advise me on cassette labelers that print 2D bar codes?
Preferences or suggestions what to look for.
Diana McCaig
Histology Lab
Chatham Kent Health Alliance
80 Grand Avenue West
Chatham. Ontario
N7L 1B7
519-352-6401 (6604)
This email communication and any files transmitted
In the past, when we made up 1% Alcian blue in 3% acetic acid (using
bottle distilled water), the pH was always 2.5. We did not have to
modify it to get the proper pH. Still using the same powder, we are
getting a pH of 2.1. I hate to adjust it because it seems to affect the
staining. Any
We had a series of PIN 4 cocktail immuno stains and got a poor reaction.
I am afraid to cut deeper in the block and miss the area of concern.
I have determined the problem was due to the heat bar not being turned
on.
What can I do the slides to reverse the process and restain them. The
DAB
Can someone provide me with the guidelines (Canadian) for scoring ER/PR
and what the preferred antibody is for determining this. I see there
are several clones.
Diana
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What should the pH range be for Scott's Tap Water?
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