Ann Specian (where?) asks about Epredia Xylene Substitute:
>>We are thinking of changing from xylene to this substitute. Does anybody
have any Processing protocols using Epredia Xylene?substitute that they
could share?<<
Well, what’s in it? You’re asking your readers to look it up for you.
I
Here's the opinion of an 85 year old pathologist who in the course of his
training spent a year doing histochemical research. In my experience,
pathologists aren't allowed much input in the selection of controls.
Anyone doing special stains needs to be able to evaluate the control slides
for
>
> Re: [Histonet] Modified Davidson
>
> The formula for "modified Davidson's fixative" that I used was three parts
tap water, three parts reagent alcohol, two parts 37% formaldehyde ("strong
formalin"), one part glacial acetic acid. Best mixed under a fume hood.
At 85 I must be one of the last
>
>
> I recall learning the technique of using 1% periodic acid to brighten up
> dismal hematoxylin staining, when I was a resident at Johns Hopkins in
> 1970. I don't know where the histochemist I learned it from got it, though
Bob Richmond
Maryville TN
John Kiernan asks:
>
> >>Bob, Why weren't they routinely buffering (or at least neutralizing) the
> formalin fixatives at Johns Hopkins as recently as 1970? - It had all been
> in the scholarly books (by Pearse, Lillie, etc) for >10 years, and was also
> in Lee Luna's 1968 Manual of Histologic
This 84 year old pathologist recalls the histopathology laboratory at Johns
Hopkins Hospital around 1970, when I was a pathology resident there.
Histotechs, often laboratory clerks, sat in front of rows of 400 mL Stender
dishes, smoking cigarettes while they hand-stained slides, often carrying
>
> Gudrun Lang in Austria asks:
>
>>Has anyone experience with Sudanblack B on paraffin slides for staining
[lipofuscin]? A doctor wants the demonstration of the lipoid content of
foamy cells or granulocytes in lung. I've found protocols that have
incubation-times from 10 minutes to over-night.
>
>
> I used a cryostat, a large, very primitive cryostate (long fleece gloves)
> at Washington University in St. Louis in 1962, in a laboratory doing the
> quantitative histochemistry techniques developed by Dr. Oliver Lowry before
> then. We cut very thick sections, around 50 or 100 µm as I
>
>
> My experience with anti-roll plates is mostly with the old International
> cryostats of days gone by. Pathologists usually disdained anti-roll plates
> and used an artist's brush to keep the section from rolling, but more
> proficient users depended on them. I learned to use them in a
>
>
> I was surprised that Dr. Freida Carson doesn't have a Wikipedia bio. Can
> somebody take care of that?
Bob Richmond
Samurai Pathologist
Maryville TN
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
>
> Christie Saunders MLS(ASCP)CMQIHC, MOHS Histotechnician in Ohio, asks:
>
> >>I may have a silly question, but I truly do not know the answer to this
> question. I work in a MOHs lab and need to know if there's a particular way
> to store unprocessed tissue in a fridge or freezer in some way
>
> Victoria Spooner at Bassett Healthcare in New York state asks:
>
> >>Does anyone have cutting protocols for mastectomies for gender dysphoria
> they would [share] with me? How many blocks are submitted per breast?<< How
> do they compare [to] mastectomies for tumor?<<
>
I don't know of any
Patients should not be given formalin. You can transfer the specimen to 70%
alcohol, and hope they don't drink it.
If you're in one of those unusual pathology services where photography is
permitted, I wonder if you could offer the patient a photograph of the
specimen by e-mail.
Bob Richmond
Dorianne Bonello, Allied Health Practitioner (MLS), Histology Laboratory -
Pathology Health-Mater Dei Hospital, on the island of Malta asks:
> >>We are experiencing freezing artifacts on our frozen sections.
> Basically, we are seeing cavity-like structures under the microscope,
> mostly
>
> Anne Murvosh HT at Advanced Dermatology asks: >>I was wondering if 10%
> formalin needed to be kept in a flammable cabinet. We never have before,
> but I wondered if we were doing it wrong or if regulations have changed.<<
>
> Formalin and neutral buffered formalin (3.7% formaldehyde in water)
>
> Bouin's fixative has no business being used in a spray bottle. It's a very
> toxic material that shouldn't be aerosolized.
>
As Dr. Steve McClain suggests, dilute acetic acid - 3 to 5%, white vinegar,
is quite sufficient for preparing tissue for inking, and isn't toxic and
messy like Bouin's
Vikki Baker (or Amy self) - where? - asks:
> >>We recently had an incident which led us to review our policy on frozen
> section QA. In your institution does the same pathologist who did the
> frozen section read the permanent [paraffin] sections? Also if they do
> then who is the pathologist
>
> Merissa (where?) asks; >>I am doing some planning for a new project and
> wanted to get opinions on fixation of large pieces of tissue. We will have
> human shoulders, where we want to preserve the rotator cuff/joint. Cutting
> the tissue with a saw will damage the soft tissue, so we were
>
> The edition of the "AFIP Manual" - Manual of Histologic Staining Methods
> of the Armed Forces Institute of Pathology, Third Edition - most of us are
> familiar with was edited by Lee G. Luna. I recall buying a copy of it in
> 1968 when I was a resident. I now have a copy of what I think is
>
> In answer to a query about tissue Gram staining, Tony Henwood adds
> instability of the iodine solution to the long list of reasons why tissue
> Gram staining doesn't work very well.
>
The Gram stain done on smears is of course one of the most useful
microtechniques in microbiology, but
>
> Brad Ringer, HTL (ASCP). histology manager at Springfield Clinic in
> Springfield IL asks:
> >>I'm curious to know how many levels your lab cuts on the following
> biopsies: prostate core, cervical, vaginal, bladder, and anus biopsies. I
> ask this because we are currently (and have been
In response to several questions and responses about amyloid staining:
I’ve always understood that sections for amyloid should be cut at 8 µm, but
could never get a histotech to cut them that thick.
I recall that unstained paraffin sections on the slide are usable for about
a month after
Michelle (where) asksi: >>We have a question about staining for H-Pylori
Using Quick Stain (Periodic acid 1%, Alician Yellow, Sodium Metabisulfate,
Toluidine Blue stock, Sodium Hydroxide) we notice what clearly looks like
the H-Pylori purple stained clusters, but after dehydration in 100% alcohol
Galina Deyneko (where? asks: >>Does anybody have experience how fix the
tissues for successful glycogen ? detection in murine and humane
cardiomyocytes. I am wondering maybe the trace of methanol in 10% formalin
will dissolve glycogen?? - What would be better process for paraffin
embedding or use
Steve A. McClain, MD at McClain Labs in Smithtown NY notes:
>>...to avoid incomplete sectioning...: ink the specimens well, using
acetic acid (vinegar) to fix the ink, thereby making the ink easier to see
in the block.<<
I don't like ink for this purpose, because it clutters up the microscopic
Tanya G. Abbott, Pathology Manager, PennState Health St. Joseph in
Reading, Pennsylvania asks:
>>Suggestions for where to buy good Giemsa controls for H. pylori?<
What I've always found satisfactory is to watch for positives in your own
material, evaluate them as possible controls, and use
Richard w. Cartun, MS, PhD, at Hartford [CT] Hospital asks:
>>What has been your experience with Hologic's Cellient instrument for
preparing cell block specimens? I understand that it is very good for
pauci-cellular specimens. However, I am concerned about using these
preparations for
Carole L Johnson, HT(ASCP)cm, QIHC(ASCP)cm at UCH/Memorial Central Hospital
in Colorado Springs asks:
>>We have been using ethanol in our lab and would like to change to using
reagent alcohol for the obvious reasons of cost and regulatory headaches. I
have been tasked with creating a
Scott A. Lindrud, MLSCM(ASCP)CTCM, Histopathology Technical Specialist at
Carris Health in central Minnesota (apparently not part of the Mayo Clinic
system) asks:
>>I was wondering if anyone would be willing to share their experience with
weekend Histology coverage for smaller Pathology labs?
Dawn Olszewski asks: >>I have been tasked to find a better solution to
transport extremities from the OR to histology. We have tried cardboard
boxes (no longer allowed) and plastic totes on rollers (too big to store
and absorb odors from the legs).<<
Mopec offers >>Pathport 3 is a stainless
I usually had hematology technologists assisting me back when I was doing
bone marrow biopsies long ago. I trained more technologists than I
remember. You always have to remind the patient that you're going to be
talking a lot because you're training a new assistant, but that it isn't
going to
Freezing sprays for frozen sections in cryostats are deplorable, but try
and get pathologists to give them up. I think that's probably why the CAP
has been reluctant to ban them.
During my career in pathology I saw more than one case where frozen
sections were inadvertently cut on tuberculous
Betsy Molinari HT, ASCP at the Texas Heart Institute in Houston asks:
>>I have a researcher that wants to stain Purkinje fibers and has requested
a Mallory-Azan stain. I have no experience with this stain. I have looked
online for information but am reaching out to you for personal advice.<<
Michelle (Shelly) Aono (at Auburn in Alabama) asks: >>Does anyone have any
experience changing from HemoDe to VWR Xylene Substitute? Did you have to
extend your processing times? By how much?
When people talk to good "recycling" of the clearing agent, does that mean
re-use? As in how often you
Amy (where?) asks: >>I was asked to do Victoria Blue stain on rodent FFPE
lung tissue to exam thickness of artery. Could anybody recommend a good
vendor of this reagent kit?<<
You can get Victoria Blue R (Colour Index 44040) from Sigma-Aldrich and
several others. I couldn't find anyone who offers
Mehndi Helgren at Dominion Pathology Laboratories in Norfolk, VA asks:
>>I'm trying to see what kind of exhaust/fume hoods people are using in
small grossing labs. We are moving into a new space and I want to make sure
the ventilation at the gross board is adequate. I don't think an actual
Cristi Rigazio asks: I was wondering if there are any tertiary institutions
out there that have set a benchmark for reprocessing tissue? We tend to be
less than 1%, but would love to see what others think is reasonable.<<
This grumpy old pathologist sez: If I'm the one doing the grossing, I
Betsy Molinari, HT (ASCP) at the Texas Heart Institute in Houston asks:
>>I have some very small pieces of tissue that are in 70% ethanol. Should I
mark them with eosin or safranin O? From what I have read the tissues were
still in formalin, and mine are already in alcohol. Can they still be
Sharon at Celligent Diagnostics in Spartanburg SC asks:
>>We are changing our GMS stain over from a Periodic acid kit to a 5%
chromic acid kit. What do the labs that use chromic acid in special
staining do with the waste/ used chromic acid?<<
I hope someone can give an authoritative answer to
Cindy McGrady at Hurley Medical Center in Flint, Michigan asks:
>>Our laboratory is experimenting with xylene free processing on our Sakura
VIP, substituting isopropanol for our xylene substitute. Our pathologists
have complained about processing, especially the biopsies, with our regular
the years
>
> Respectfully,
>
> Colleen Forster
> U of MN
>
> On Wed, Feb 13, 2019 at 4:35 PM Bob Richmond via Histonet <
> histonet@lists.utsouthwestern.edu> wrote:
>
>> John Kiernan, certainly glad to see you back on HistoNet! - At 80 I've
>> f
John Kiernan, certainly glad to see you back on HistoNet! - At 80 I've
finally retired.
This Biological Stain Commission glossary is a really useful resource I
wish we'd had long ago. A lot of information in it difficult to get
elsewhere. I'll link it on Facebook and on Sermo.
Two suggestions:
Karen Heckford HT ASCP CE at St. Mary's Medical Center in San Francisco, CA
asks:
>>One of my pathologists wants me to do some ER/PR's on 9 year old tissue
blocks. I know ER and PR can be sensitive are the IHC's going to work or
will there be too much antigen decay?<<
You can only try. There
4, 2019 at 6:40 PM John Garratt wrote:
> Be aware that validation of IHC should be performed if you are changing
> your processing protocol by adding a dye to the reagents or to a
> pre-processed tissue. Be cautious!
>
>
> John
>
>
>
> On Saturday, January 12
Gareth Davis asked about marking small GI specimens with dye when grossing
them.
I've used safranin O - the solution the microbiologists use in the Gram
stain. If you walk down the hall to the micro lab you can get a small
amount to try out.
Do not use eosin for this purpose. Eosin's brilliant
Gareth Davis asked about dyes to use to mark small GI biopsy specimens to
make sure they're recovered during embedding.
I've had good results marking small specimens with the solution of safranin
O that's used in the microbiologists' Gram stain. Go to the micro lab and
ask for a small amount of
Anne Murvosh HT at Advanced Dermatology & Skin Surgery in Washington state
asks:
>>We are starting to keep our melanomas in-house now that we have a better
processor, however I could use some tips or tricks on cutting large fatty
skin ellipse specimens. My problem I think, is too small a knife,
Charles Riley BS HT, HTL(ASCP)CM, Histopathology Coordinator/ Mohs
(where?) asks:
>>How does everyone gross and process your breast lumpectomy / mastectomy
specimens?<<
These are extremely complex and exacting procedures. It's your
pathologist's job to do this, and your pathologist can't
nal health policy. Institutions may also choose whether to use
> special equipment for
> such patients and what type(s) of equipment to use.
> Evidence of Compliance:
> ✓ Written policy for handling of bariatric patients
>
> ____
> From: Bo
I don't understand Lorraine Smallwood's question:
>>Can anyone give me info on the CAP inspection packet regarding policy for
bariatric patient for autopsy? I am a new "Histonet" junkie so any help
from the experts will be greatly appreciated.<<
CAP inspections don't concern themselves with
Linda Miller posts in what appears to be an advertisement:
>>New! Bouin's Fixative Substitute is a low-hazard replacement for Bouin's
Fixative. This substitute provides all the benefits of Bouin's without the
use of picric acid. Available in a variety of sizes and pre-filled specimen
Pam Barker issues one more of her frequent appeals for histotechnologists.
I can't remember when I last heard of a histotechnologist looking for a job.
>From the perspective of a retired pathologist in his 80th year: we'll get
enough good people in histotechnology when we start paying
Joseph A. Esposito at McClain Laboratories on Long Island asks:
>>The laboratory I work at has been using the Diff Quik for years now as a
stain for fine needle aspirates. Recently, when we tried to reorder a Diff
Quik stain kit from our usual suppliers, we have found it to be on
backorder. This
Chris Mason (where?) asks: >>Would anyone be willing to share their
protocol for the sectioning of Hirschprung's cases and the use of
calretinin? Our pathologists want to begin using this technique. We are
thinking of alternating H and unstained to be used for calretinin in the
case of
Tasha Campbell, B.S.,HTL(ASCP), at Frederick Gastroenterology Associates in
Frederick, Maryland asks:
>>Is nuclear fast red the only counter stain for the Prussian blue stain? I
have a Masson's trichrome kit and was wondering if [Biebrich] scarlet could
be [used as] a counterstain. I won't be
Amy Self, Histology Lab Senior Tech at Tidelands Georgetown Memorial
Hospital in Georgetown SC asks:
>>I am looking for ideas/suggestions for QM Histology/Pathology. My QM
director wants me to "measure" something that I can place on the lab
dashboard.<<
Look at the August 2017 number of CAP
Tim Morken (Pathology Site Manager, Parnassus - Supervisor, Electron
Microscopy/Neuromuscular Special Studies Department of Pathology - UC San
Francisco Medical Center) asks:
>>We have a debate going on for those freezer-stored powdered chemicals
used for enzyme histochemistry. One side says warm
Cheryl Kerry, HT(ASCP) in Houston TX asks:
>>A client wants us to start reading peripheral neuropathy biopsies. Hoping
I don't have to start from scratch - anyone have processing and prep
procedures including cutting protocols?<<
This is a highly complicated procedure, often involving
Jamie Watson, you need to clarify this question: >> Does anyone know what
percentage of labs use ethanol vs. denatured alcohol or isopropyl alcohol
on the tissue processor?<<
100% ethanol is perfectly OK, but it requires a lot of regulator compliance
because you can drink it (though you
Carl Hobbs FIBMS, Histology and Imaging Manager at Kings College in London
replies:
>>That's a good point, Bob (mouse amyloid controls for human sections). The
amyloid produced by the the various mouse models (TASTPM, TGs) is human
amyloid... as you know. I suspect that it wouldn't be accepted as
Tyrone Genade in Orange City, Iowa asks:
>>Can the Wright-Giemsa stain be used on fixed, paraffin embedded sections?
Does anyone have a protocol? I want to examine hematopoietic tissue of
fish, i.e. the head kidney. No smears or imprint possible. I would like to
use Wrights so I can use the same
Amy Self, Histology Lab Senior Tech, Tidelands Georgetown Memorial Hospital
in Georgetown, SC asks:
>>I am working on our billing process in hopes to improve things and make
it a little more efficient for us. We really have room for improvement. I
feel there is lots of work that is being done
Terri L. Braud, HT(ASCP), Anatomic Pathology Supervisor at Holy Redeemer
Hospital in Meadowbrook PA notes:
>>Our policy calls for wiping of forceps with gauze between cases at gross
and at embedding. At gross, we use a disposable absorbent lined pad on the
cutting board for each larger case, and
If you choose another oxidizing agent than CrO3 (such as KMnO4, potassium
permanganate) it's up to you either to find literature to back you up, or
to do the stain with appropriate controls for the fungus you're looking for.
Freida Carson (citation below) found that periodic acid, commonly
Martha Ward at Wake Forest Baptist Health, Winston-Salem, North Carolina
asks:
>>I am posting this question for our Histology manager. For prostate needle
biopsies how many levels and unstained slides are people cutting and also
how long after the case is signed out is everyone keeping the
With his permission I post pathologist Leon Metlay's Facebook obituary of
his wife's father:
My father-in-law, Dr. Bernard Leon Klionsky, died [November 11th, 2017] at
the age of 92. He was one of the unsung heroes of pathology. As a young
man, he invented the form of cryostat that we all use to
The old Samurai Pathologist has a copy of Ann Preece's book. I was
contemptuous of it as an arrogant young pathologist of 28, deeply
respectful of it as an arrogant old pathologist of 78. But it's a reproach
that a fifty year old book has not been superseded.
Bob Richmond
Samurai Pathologist
Amy Self, Histology Lab Senior Tech, Tidelands Georgetown Memorial
Hospital, Georgetown SC asks:
>>How is everyone storing their amputated limbs that are received in
pathology? Are they stored in the morgue or in a refrigerator located
within the department and at what temperature is suggested
Elizabeth, I certainly wasn't talking about volunteer platelet donors, a
totally different, very dedicated bunch. I would continue to observe that
plasma centers are located in fairly sleazy parts of town.
I wish I could continue to be a donor - whole blood, because I'm a rare
donor (group O, and
I had no idea that there was a shortage of immune globulin. When I was with
Red Cross in the 1970s, we were awash in it, though only a few batches were
usable IV, a technology that was just developing then.
If we disrupt the health care payment system, the plight of our
hemophiliacs will be
Jorge A. Santiago-Blay, PhD asks about blood donation for money. I suppose
he's in the US. I don't think there's any paid donation of whole blood in
the US any more. This is probably a plasmapheresis center, where people
donate twice a week. The red blood cells are returned to the donor. Two
Richard W. Cartun, MS, PhD - Director, Histology & The Martin M. Berman, MD
Immunopathology & Morphologic Proteomics Laboratory - Director, Biospecimen
Collection Programs - Assistant Director, Anatomic Pathology, Hartford
Hospital, Hartford, CT asks
>>Anyone using ClearRite (xylene replacement)
From: jdhanna...@gmail.com
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Coagulants question
Message-ID:
Content-Type: text/plain; charset=us-ascii
"jdhannasch" (who) asks:
>>Can someone explain to me what a coagulant vs a
Lauren Sweeney at the University of Georgia asks:
>>Blades for grossing tissues- anyone have recommendations? The vendor that
we were purchasing just straight razor blades from has stopped
manufacturing them. We don't use scalpels because of their higher cost and
we are only working with poultry
Lori Jones, CT(ASCP), Pathology Supervisor, Ingalls Memorial Hospital asks:
>>We use Bouin's Solution in our pathology department and are currently
disposing of it by neutralizing it with Vytac for formalin. I can't find
supporting documentation that this is the proper way to dispose of it. I'd
Warda Hassan (where?) >>would like to have some advice from expert from the
field of pathology on microscope selection. Which one would you select as a
manufacturer for microscopes?<<
Speaking from more than 50 years of going to and fro in the world of
pathology, and walking up and down in it
Tim Morken in pathology at UC San Francisco Medical Center asks about the
Hirsch-Pfeiffer (correct spelling) cresyl violet stain for frozen sections.
"I've found many references to it, but none that give the procedure. And
the original paper is from 1955 not easily available. And is in German."
Charles Riley HT, HTL(ASCP)CM, a Mohs histopathology coordinator, asks:
>>Can anyone give me an idea how they process cystic tissues? The normal tissue
processes extremely well on my current protocol but the cystic areas just
are too soft to cut. Any tricks anyone can provide to process better or
Tim describes a problem "I have a pathologist that is not happy with the
fixation on some of our LEEP specimens."
LEEP specimens are inherently crappy, because of the cautery used to obtain
them, and the resulting cautery artifact in the specimens. In the last few
years they've turned the voltage
A few years ago the B/R spinning-band stills were definitely the still of
choice for recovering histologic solvents, and the older generation of CBG
machine were inadequate. I think though that the later generation of CBG
stills predominates today. I don't know how they work. Could somebody give
>
> Lucie Guernsey at UC San Diego asks about sodium borohydride:
>>I'm currently going over IHC SOPs that were written by lab members that
have long ago moved on to other jobs. One inconsistency that I've come
across is the use of 0.5 % sodium borohydride in immunofluorescence.<<
Does your
The old Samurai Pathologist - now retiring at 78 - thanks the many
histotechnologists who've kept him out of hot water the past 52 years.
Too bad we can't have more kids in search of a career reading Histonet - or
at least, the Help Desperately Needed notices!
Bob Richmond
Samurai Pathologist
Gudrun Lang (in Austria) asks:
>>I wonder how widespread the usage of eosin B is in H protocols. Is
there a
specific difference in application to Eosin Y?<<
Eosin B is closely related to the more commonly used eosin Y. As the
letters imply, it's Bluish rather than Yellowish.
I've never seen
Charles Riley HT(ASCP)CM asks:
>>What is the best way to handle breast specimens that were grossed too
thick
and did not process well? Our medical director does not want us to
reprocess the tissue but it is almost impossible to get even a remotely
decent section. If anyone has any other tips
Jessica Piche, HT(ASCP) at Waterbury Hospital [Connecticut] asks:
>>Just wondering what kind of Harris Hematoxylin people are using. We are
doing a regressive H on a Leica Autostainer XL for 9 minutes. We have
been buying Ricca Hematoxylin but we are having so many issues with it. Are
people
>
> Terri L. Braud, HT(ASCP). Anatomic Pathology Supervisor, Holy Redeemer
> Hospital, Meadowbrook PA describes:
>
> >>We use an awesome little band saw made by IMEB, Inc. It has a small
> foot print, 4 blade types and added accessories for a super lab bone
> cutting station, and best of all,
>>Lisa Hamilton asks: In the past I have seen clip-on magnifiers that are
used to embed tissue. Of course now that I need one I cannot remember what
catalog I saw them in! I was hoping someone might.<<
If you're looking for something that fits over your head and puts lenses in
front of your eyes
Further researching the topic, I've learned that there are two recently
introduced non-radioactive alternatives, Savi Scout and Sentimag. I don't
understand how they work.
Coincidentally, I received a circular in this morning's mail with
information about a continuing medical education event on
Jim Vickroy, Histology Manager at Springfield [Illinois] Clinic asks: "Our
organization is looking into the workflow necessary to handle breast
lumpectomies with radioactive seed localization (RSL)".
Thanks for the heads-up - as usual, pathologists and histologists don't get
told. Nursing
Angela Lamberth at the La Jolla [California] Institute for Allergy &
Immunology asks:
>>I'm gearing up to perform a pentachrome stain. I will be making this in
house and not using a kit. Through searching histonet, I've found a
protocol used by the Children?s Hospital of Philadelphia Pathology
Elizabeth M. Cameron, HT(ASCP), QIHCCM. Lead Histologist at Mid Coast
Hospital in Brunswick, Maine asks:
>>I have been staining fish tissues fixed in Davidson's fixative with H,
and the researcher would like the eosin to be more intense. Our standard
protocol works well for our own tissue, but
Here's John Kiernan's extremely informative review of gallocyanine (that's
how he says it's to be spelled) from the archives - I can't find a date on
it. Really tells you everything you need to know to do Nissl staining with
it.
Liz Chlipala at Premier Laboratory in Boulder CO writes:
>>We have run this stain [gallocyanin] before, purchased the reagent from
Sigma, it's pretty easy to do there is a procedure in Bancroft and Gamble.<<
What stain? What mordant (chrome, aluminum, none)? To stain what?
I think the person
Eva Permaul at Georgetown University asks:
>>We just had a request for Gallocyanine staining. Does anyone do this? Can
you share your protocol? Where do you buy your reagents?<<
Gallocyanin (correct spelling - C.I. 51030) is a blue oxazine dye somewhat
similar to celestin blue B. It's been used
Jillian A. Russell, HT (ASCP)CM, QIHCCM, Supervisor, CDx Histology
Operations, R at Dako in Carpinteria CA asks:
>>I am wondering how many labs are using B-5 fixatives and how many are
using B-5 alternatives due to the mercury issue? - For those who have
switched to an alternative, have you
Steve A. McClain, MD asks:
>>The next 3 weeks we are turning our lab cameras and our specimens toward
making a 360 photographic orbits around specimens to create a 360 stitched
image or video.
If you know any pathologists who have tried 360 imaging around a specimen,
kindly send me their name. I
Jeff Halstead at Oregon Health & Science University asks:
"Some time ago info on the list discussed placing eosin or other dyes in
the processor and I was wondering what everyone is actually using. Heard
safranin o was a good idea . any thoughts?"
Safranin O - the solution your microbiology
Jeff Halstead at Oregon Health & Science University asks:
"Some time ago info on the list discussed placing eosin or other dyes in
the processor and I was wondering what everyone is actually using. Heard
safranin o was a good idea . any thoughts?"
Some time ago I worked in a lab that used
Rebecca Ashley at the Wyoming State Vet Lab in Laramie asks >> I had a
biopsy today that was nearly impossible to see on the sponges during
embedding or in the block. I've heard mention of marking these with eosin
to make them easier to see. Has anyone done this? Or do you use some other
type of
s.
>
> Why not just standardize it from the start, reagent, pH, temperature and
> it really cannot fail.
>
> Spokane Ray
>
> --
> *From: *"Bob Richmond via Histonet" <histonet@lists.utsouthwestern.edu>
> *To: *"Histone
1 - 100 of 113 matches
Mail list logo