.. 50ml
Sodium hydroxide 1%... 0.5ml
Filter and use within 15 minutes.
On Thu, Jun 20, 2024 at 9:31 AM Greg Dobbin wrote:
> Good day John,
> Very nice to hear from you again! I have been consulting your textbook in
> my investigations!
> Sorry about the brevity of the
re they using "at another
> lab" to get correct red amyloid that is green (dichroic, not fluorescent)
> with crossed polars?
> *John Kiernan*
>
> https://www.schulich.uwo.ca/anatomy//people/faculty/emeriti/kiernan_john.html
> = = =
>
te ethanol, 6 dips
each.
Dip the slide 10 times in a coplin of xylene.
Continue dehydrating the other slides.
Coverslip the slides.
*Greg Dobbin*
1205 Pleasant Grove Rd
Route 220
York, PE C0A 1P0
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pieces of tonsil, pancreas, small bowel and liver.
*Greg Dobbin*
1205 Pleasant Grove Rd
Route 220
York, PE C0A 1P0
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Decant formalin off into formalin waste containers and the remaining tissue
go into a red bag (red signifying destined for incineration). As the O.R.
does with fresh tissues for disposal.
*Greg Dobbin*
1205 Pleasant Grove Rd
Route 220
York, PE C0A 1P0
Use a formic acid based decal solution and MAKE SURE the specimen does not
fix (formalin fixation) longer than 32hrs (false negatives result). Use 70%
ETOH to manage the fixation time (ie fix for 24 hours, decal for 4 hrs,
place in 70% ETOH until it gets put on the processor. Hold in 70% ETOH for
and then
run slides on your IHC platform as you would -without the dewax step
obviously. :-)
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*If God made a drink better than whiskey he kept it for himself! *
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We use the same. Our protocol is ER2 for 15 mins. We have 3 washes after
polymer.
Greg
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*If God made a drink better than whiskey he kept it for himself! *
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Since images cannot be attached, if any of you feel you have some
experience that I may find helpful...please email me directly and I will
attach the image to my reply.
Thanks again,
*Greg Dobbin*
Chief Technologist
Anatomic Pathology
Queen Elizabeth Hospital
Charlottetown, PE, Canada
!
Any ideas?
Thanks,
*Greg Dobbin*
Chief Technologist
Anatomic Pathology
Queen Elizabeth Hospital
Charlottetown, PE, Canada
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the control section perform? As expected or same artefact?
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*If God made a drink better than whiskey he kept it for himself! *
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http
issue discards.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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specimens are split between Cytology and
Histology...the histo specimens go directly into formalin.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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until they can be processed into paraffin.
My questions:
Is anyone else doing this??
Is 70% ETOH still a viable option for labs in this situation?? And…
Is there another idea and/or more information out there that could help us
in this regard??
Thank you,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove
director was looking for suggestions for quality
indicators to report and while I feel like our cold ischemic average time
is impressive at ~17 mins, she says that is pretty standard for everyone.*
Thanks,
Greg
--
*Greg Dobbin*
Chief Technologist - Anatomic Pathology
Queen Elizabeth Hospital
,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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unostainer. Hope this helps.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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comparisons between old
and new processors (the downside of what is otherwise an exciting time!).
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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e reagents then it is a
defective valve or line for that reagent.
I hope this was helpful.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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Garratt wrote:
> Evaluation of Virus Inactivation by Formaldehyde to Enhance Biosafety of
> Diagnostic Electron Microscopy
>
>
> https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353909/
>
>
> It is nice to have a reference.
>
>
>
> John
>
> On Thu, Aug 6,
Hi Amy,
Formalin fixed tissue is no longer infectious...unless you are talking
about prions (eg scrapie, BSE, etc). So there should otherwise be no
concerns or additional precautions required.
Cheers,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything
,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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that switch
should be an easy and cost-effecient thing to try first.
Good luck,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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stain) would likely remove parts or all of the section.
All the best,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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not drain out on standing and does not drain or evaporate when baking
at 60C. If the slide with trapped water is put on the instrument with
trapped water, the dewax step will lift much of the tissue.
Cheers,
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything
ons with the same AR (eg
1:10, 1:25 and 1:50). Once you get close to where you think the intensity
should be you can try modifying the AR protocol to improve the sensitivity.
Good luck,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation its
tonsil kept in
> formalin before processing? Could over fixation be the issue?
> I have found that maintaining tight control of control tissues is
> important which includes minimum and maximum fixation time.
>
> John
>
> Sent from ProtonMail Mobile
>
>
> On Tue, May 7,
this schedule that is particularly concerning?*
Thank you,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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think its a big deal.
>
> First how would you handle the issue given the frisge has been restored ?
>
>
>
>
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
___
l for both ER and PR. It
seems to me that if the internal control is staining adequately, then
perhaps interpretation will not be an issue. I am curious, does anyone have
a different take on relying the internal control as a guide in this
particular situation??
Greg
--
*Greg Dobbin*
1205 Pleasant G
and no
additional retrieval.
Cheers,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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Hi Dr. Cartun,
It has been many years since I worked in EM but I my recollection is that
tissues could remain in 2% Glut indefinitely without detriment (for EM
purposes). However, Osmium tetroxide had to have a limited exposure.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A
? Could a new person be putting undiluted Bond Wash
in the bulk container?
Let us know what you find out. Good luck.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself
1:100 with ER-2 for 30 mins.
Clone is the V600E from Spring BioScience
Looks great for uis and we are performing well on EQA surveys.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself
Spring Diagnostics. We run it on the Bond platforms at 1:100 with ER-2
> (high pH) for 30 mins.
>
> Greg
>
>
>
> --
>
> *Greg Dobbin*
> 1205 Pleasant Grove Rd
> RR#2 York,
> PE C0A 1P0
>
>
>
> *Everything in moderation...even moderation itsel
Here in Charlottetown we are using V600E (VE-1) clone (Monoclonal) from
Spring Diagnostics. We run it on the Bond platforms at 1:100 with ER-2
(high pH) for 30 mins.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself
Pass The General MLT Certification exam, as our MLT exam includes Histology
and Microbiology. :-)
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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cases.
Thank you for your time!
Greg
--
*Greg Dobbin, MLT*
Chief Technologist,
Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
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of intensity
over two years even. For me, the antibody expires long before the any
deterioration of signal is noticed.
In your case, if you are using a commercially prepared diluent, then start
looking at extended times left out of the fridge, a malfunctioning fridge,
contamination, etc.
Greg
--
*Greg
Hi Laurie,
We are purchasing the antibody only from Roche/Ventana and optimizing it
for use with our detection system (Bond Refine Detection kit) and the
Bond-III stainer. Ask your Ventana person about buying the Ab only.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
not be an issue if you
are able to obtain good sections. Have you stained these poorly infiltrated
specimens with H? Are you certain you have good sections with all tissue
components represented? That would be my main concern.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
the drawer.
Hope this helps,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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with your Director to find that balance
between cost (ie more slides = increased cost) with confidence (how many do
you need to see in order to feel confident that the stain is performing as
expected).
I hope this helps.
Sincerely,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE
No pretreatments for anything that is not formalin fixed. I think 95% ETOH
for a fixative but but others may have a better idea than I.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself
have any
adverse affect on the stainability of AFB organisms if present?
Thank you,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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marrow
specimens only stains plasma cells it does *NOT* stain B-cells. So this is
likely why LN tend to be negative. Maybe one of our Histonet-contributing
pathologists would like to elaborate? :-)
Greg
--
*Greg Dobbin*
Chief Technologist,
Anatomic Pathology
Dept. of Laboratory Medicine,
Queen
ould be for me to
share our protocol. Let me know if you would like me to send that to you.
Cheers,
Greg
--
*Greg Dobbin, R.T.*
Chief Technologist,
Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902)
, in a box,
wrapped, stacked, etc)?
Thank you,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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before processing. We use the
same slides for Special Stains and don't have this issue there.
I need some new suggestions to try! All ideas welcome.
Cheers,
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself
for pick up.
Greg
--
*Greg Dobbin*
1205 Pleasant Grove Rd
RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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in the freezer for a little longer to avoid freezer burn.
Cheers,
Greg
--
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RR#2 York,
PE C0A 1P0
*Everything in moderation...even moderation itself**!*
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tact Leica Tech
support to try to figure out what went wrong the first time. If it is not
corrected, then you are back to suspecting a pre-analytic issue (assuming
you are not seeing this uneven-ness in other IHC specimens). I strongly
encourage use of tissue controls on every patient slide.
Cheers,
Greg
-
Judith,
The red chromagen is suseptible to "fading" if stained slides are left in
either alcohol or xylene for too long. Check to make sure that everyone
involved is following the same procedure for the dehydraytion, clearing and
mounting of the stained slides.
Greg
--
*Greg Do
Buy yourself a roll of WHMIS labels. Get ones that are sufficiently large
to be easily read while still fitting on the side of the secondary
container. All necessary info will be captured there once you check the
right boxes, etc.
Cheers,
Greg
--
Greg Dobbin, R.T.
Chief Technologist,
Anatomic
)
benchmark for all to strive for as their minimum.
Cheers,
Greg
--
Greg Dobbin, R.T.
Chief Technologist,
Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
*Everything in moderation...even
that
will work with my printer??
Thank you,
Greg Dobbin
Chief Technologist,
Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
*Everything in moderation...even moderation itself
Are you soaking your blocks in dilute ammonium hydroxide before sectioning?
Soaking too long will affect stain quality.
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894
really not trying to be sarcastic in anyway.
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work
Thanks Joyce. This excerpt supports what I had said- noting the
difference between the negative (or deletion) control (which is what I
was addressing in my reply) and the negative tissue control.
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine
The Bond does do ISH. In fact it utilizes the same detection kit so you have
only to buy the probes, not the additional detection kit that could (depending
on your volume of ISH requests) expire.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen
the other 9 positions remain functional.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem
Cynthia,
Hematoxylin will inactivate the peroxidase (link) in the tissues. You must go
back and re-do the link step and hopefully the antigenic sites will still
accept more streptavidin (or similar) conjugated antibody.
Cheer.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept
I should add that the DAB step may also have quenched all of the linked
peroxidases even before the hematoxilin was added (which would finish off any
that remained).
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box
some feedback on this one.
Thanks so much,
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I
as far as I am aware. I have no experience with the
affects on histological preparations.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find
Hey Pam,
No problem, I will. Nice to hear someone south of our border has heard
of Canada's smallest province!! :-)
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894
reports, 2 years? 20 years?? What are others doing in this
regard?
Thanks.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find
experience.
good luck.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have.
- Thomas
I agree with Renee. It will proabaly be at least as costly to have to
re-validate everything!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
.
Thank you!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have.
- Thomas Jefferson
Almost always receive on time. I can think of only one instance in a
year and a half where anything was on back order (it was an antibody).
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A
Alcohol based suggests to me an absence of formalin. In which case,
epitope retreival is not indicated.
Also, you didn't say if it had been working and stopped or if this was
a new marker for your lab.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine
I echo Joyce's comments!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have
drab Wednesday afternoon.
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have
Oh my gosh! You're right. My day is suddenly not so drab!! LOL
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work
-coverslip slides. But since I switched to using the premium
grade year round (as opposed to only in the more humid months, which is
what I was doing to try andsave money!) I have had almost no glitches at
all!
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept
trying to make sure that the tissue is flat in the mold (ie pressing the
tissue down). Has anyone else out there have any similar experience with
this problem? Is the solution as simple as cutting smaller pieces into
the cassette at the time of trimming?
Thanks.
Greg
Greg Dobbin, R.T.
Chief
I am positive no freezing spray being used.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I
Yes. ??
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have.
- Thomas Jefferson
Hi Vanessa,
Yes! I have our eosin staining down to just 10 secs! I am considering
just letting the slides hover over top of the eosin for a minute instead
of actually dipping! LOL
Very strong indeed.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen
I echo everything Julie said!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more luck I seem to have
I guess I would have to echo that as well!
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I work, the
more
for subsequent processing.
I look forward to reading your knowledgeable replies.
Have a nice weekend everyone.
Sincerely,
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894
300.
Format: Mouse ascites
Size: 0.1, 0.5 and 1 mg
Expiration: One year from date of QC release.
Storage: Store at 2-7°C. Do not freeze!
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
The CV5030 works very well for us-as long as we spend a little more
buying the higher grade coverslips that don't tend to be affected by
humidity as much.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
). Hopefully the 4% paraform. works. Is methanol
fixation an option??
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
I find that the harder I
instruments (they know who they are) require you to buy an entire
separate detection system to do ISH and so if your volumes for ISH are
low, you will waste a lot of money in expired kits.
Cheers.
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth
Hi Folks,
What's out there? What's hot and what's not? Anyone using their
cytology autostainer for histology special stains? Welcome all input
(including vendors).
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O
Hi Paula,
You really have to tell us which instrument you are using to get a
concise answer. Other details like how the slides are dewaxed for
instance would also definately help.
Regards,
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth
Hi Jennifer,
Your Ventana Application Specialist should be more than willing to help
you thru this process. I demo'd an XT last year and I recall
double-staining was very straight forward. Unfortunately the details of
which were not retained by me!
Good luck.
Greg
Greg Dobbin, R.T.
Chief
accomplished his mission!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
And in the end it's not the years in your life
that count. It's the life
of this response
necessarily addresses either CAP or CLIA regulations).
Cheers!
Greg
Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385
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