Hello everyone!
We have a referring clinician that is concerned about leaving his specimens in
an outdoor lockbox in the summer because the formalin will get hot. I don't
think that having some specimens in formalin in hot weather would cause any
problems but I can't find any references one wa
Hi Vanessa! It's funny that you asked this question because we were just
talking about this a few days ago in my lab. Our tables are low and we all
sit. We were discussing that we would like to have higher tables so that we
could have the option to stand or sit on a higher chair. Since we ar
Good morning all!
We are having a problem with our H&E. My chief pathologist believes that we
have day to day variations in intensity as well as variations from slide to
slide (even within a rack), and that the hematoxylin gets darker as the week
goes on. We use 2 automated Sakura Prisma str
Good morning histoland!
Has anyone had success with the ROS1 antibody from CellSignaling? I just can't
seem to get it working beyond what our pathologist call "a faint blush". I
would greatly appreciate if you would be wiling to share your protocol!
Have a lovely Monday!
Erin
Erin Martin
Hello all,
Would anyone be willing to share how they track workload? Spreadsheet?
Database? Our volume has recently increased and I am looking for a way to track
individual output so that I can distribute work and rotate tasks fairly. I
don't want to have my "fast" people going out with repet
Good morning histonetters!
I'm looking for a new source for HHV-8 (KSV), clone 13B10, antibody.
CellMarque's is no longer IVD, nor is Ventana. Does anyone have a suggestion?
Thank you!
Erin Martin, Histology Supervisor
UCSF Dermatopathology and Oral Pathology Service
1701 Divisadero St, S
Hi all,
Does anyone know of a source for a Leishmaniasis control block or control
slides for IHC?
Thanks in advance!
Erin Martin, Histology Supervisor
UCSF Dermatopathology and Oral Pathology Service
1701 Divisadero St, San Francisco, CA 94044
415-353-7248
Confidentiality Notice
The inf
Good morning everyone!
One of my pathologists says that we are having a problem with the tissue on the
slides looking vacuolated and torn. He is convinced it is from microtomy.
Anyone have any ideas? I was thinking that it might be a processing issue.
Thanks in advance!
Erin Martin, Histo
Hi all!
Santa Cruz Biotech has to discontinue all goat and rabbit antibody production:
http://blogs.sciencemag.org/pipeline/archives/2016/05/23/trouble-at-santa-cruz-biotechnology
I hope you are all having a great Tuesday!
Erin
Erin Martin, Histology Supervisor
UCSF Dermatopathology a
Good morning! My pathologists would like us to cut formalin fixed (not yet
processed) tonsil tissue on a cryostat for DIF staining. Has anyone done this?
I did a quick search that seemed to indicate that it was possible but that the
architecture of the cells would be altered because of ice cr
Hi Bernice!
A 1:1 acetone xylene solution does indeed dissolve the plastic film Sakura
coverslip. No need to buy any book.
The old - 1990's - film coverslips had a problem (that I believe Sakura has
corrected) which caused the coverslip to lift off the slide and take the tissue
with it.
Good morning! I agree with some of the other comments - "per day" is too
variable because of tissue type, overall volume, etc. We use hourly average to
try to keep everyone in the same range but still leave room for individual
abilities.
Erin
Erin Martin, Histology Supervisor
UCSF Derma
Good morning all! Would anyone mind sharing their plans for power failure? We
have backup generator power on red plugs but my pathologists want a plan for
what we would do if the power went out AND the backup generator failed.
Thanks for your help!
Erin
Erin Martin, Histology Supervisor
We don't have a need to pin where I currently work but at past labs I have used
flat pieces of foam, like the lids from cooler boxes that used to ship reagents
that are temperature sensitive. You can cut them to fit whatever container you
are going to use to fix the specimen. Place a few paper
Good morning all,
I posted yesterday regarding the use of benzidine for the detection of
hemoglobin. My pathologist believes that standard DAB can be used instead of
benzidine solution but I can't find any references for using DAB as a
hemoglobin stain. Do any of you fine histo folks do thi
ely. Does anyone have a protocol
that might give the same results?
Thank you,
Erin Martin
Erin Martin, Histology Supervisor
UCSF Dermatopathology Service
415-353-7248
Am J Dermatopathol. 1995 Aug;17(4):362-7.
Benzidine stain for the histochemical detection of hemoglobin in splinter
requirements and therefore
still want to see negative controls. Has anyone by inspected recently by TJC
and had this issue come up?
Thank you!
Erin Martin
Erin Martin, Histology Supervisor
UCSF Dermatopathology Service
415-353-7248
Confidentiality Notice
The information transmitted is intended
No open flames.
Erin Martin, Histology Supervisor
UCSF Dermatopathology Service
415-353-7248
Confidentiality Notice
The information transmitted is intended only for the person or entity to which
it is addressed and may contain confidential and/or priviledged material. Any
review, retransmis
We use a 50% solution of Nair in water to soak nail blocks after we have faced
into them. Then albumin to keep them on the slides. Works great!
Erin Martin, Histology Supervisor
UCSF Dermatopathology Service
415-353-7248
Confidentiality Notice
The information transmitted is intended only fo
Good morning all!
One of our fellows emailed me a question that she came across while studying
for her boards:
"I'm studying for my board exam and came across questions re: paraffin
embedding.
It reads: best temperature for paraffin embedding is
38-48
48-58
58-70.
I am getting some info on In
Happy Monday!
We get ours from BioCare.
-Erin
Erin Martin, Histology Supervisor
UCSF Dermatopathology Service
415-353-7248
Confidentiality Notice
The information transmitted is intended only for the person or entity to which
it is addressed and may contain confidential and/or priviledged
Hi everyone, Several people have contacted me regarding the article I mentioned
in my post yesterday. Here are the details:
Immunofluorescence With Dual Microwave Retrieval of Paraffin-Embedded Sections
in the Assessment of Human Renal Biopsy Specimens
AJCP 2013 139:71-78; doi:10.1309/AJCPRZ
Hello all,
My pathologist gave me a copy of "Immunofluorescence with Dual Microwave
Retrieval of Paraffin-Embedded Sections in the Assessment of Human Renal Biopsy
Specimens" from the American Journal of Clinical Pathology. He said that the
same principle should work on skin and he would lik
Hi,
We have been processing xylene free for a couple of years in ThermoFisher
Excelsior processors. The tissue goes directly from isopropyl alcohol to
paraffin. It works well for us. We sought out a xylene free protocol to
reduce the amount of xylene in the lab.
We do need to use xylene
Hi histonetters!
Our pathologists want to turn around skin biopsies same day and are again
looking at microwave processors. Due to a bad past experience, I'm not
enthused but perhaps there is someone out there who loves their microwave
processor? Even on derm? Or has anyone worked out a good
We have been processing without xylene on ThermoFisher Excelsior processors for
a couple of years. We go directly from 100% isopropyl alcohol into paraffin.
A thermo sales rep should be able to give you some literature on this.
When we first got the processors we did side by side validation
Good morning everyone,
Does anyone use MCP antibody (Merkel Cell Polyoma Virus) from a vendor other
than Santa Cruz Biotech? If so, would you please let me know your source?
Thank you!
Erin
Erin Martin, Histology Supervisor
UCSF Department of Dermatopathology
415-353-7248
Hi all,
More questions on FISH. How does one go about validating an ASR probe on FFPE
tissue? I have no FISH experience and therefore am starting from scratch. The
specific probes that our pathologists are interested in are: t(14;18),
t(17;22) and t(2;5).
Also, does anyone know what ed
Hello all,
Does anyone have a working non-Ventana protocol for this antibody? We need
Dako. We got it working at 1:100, HIER in Dako pH9, antibody incubate 30 min,
Envision Dual Link 30 min but the researcher who wants it says that it produces
uneven staining on the test tissue. She wants it
Good morning!
We are having a lot of trouble with one of our Microm 355S microtomes. It
advances forward at random times so that it ends up chunking into the block.
The first time we had a repair person in, he was skeptical that it was moving
on its own - until it did it to him! Since then,
Hi,
In our lab, the water is tested every 6 months. If it fails, we disinfect the
DI dispenser (to rule out that the nozzle was contaminated) and resubmit a
sample to micro. If it fails second time we would would contact the vendor to
figure out what the problem is - we've never had to go tha
Hi all,
I'm having a problem with my PAS stain. My pathologist says that glycogen and
fungus stain beautifully but basement membranes are pale. We are using 0.5%
periodic acid for 10 minutes and schiff's for 25 minutes followed by 5 min
rinse in warm/hot water. Any thoughts? Thank you in ad
cal
regulatory agency, which would make it easier for them to give you guidance.
Erin Martin
Erin Martin, Histology Supervisor
UCSF Department of Dermatopathology
415-353-7248
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Hello everone,
We recently stained about 20 slides with Fontana for a research project. They
were all fine except for 3 or 4 slides on which the pathologist says that the
stratum corneum is overstained. The rest of the tissue is fine but that layer
is too black. Now I have to fix the problem.
Has anyone run into a problem or artifact from freezing spray? I think we may
be having a problem with it but I can't find any pictures or descriptions of
what it looks like.
Thanks in advance,
Erin
Erin Martin, Histology Supervisor
UCSF Department of Dermatopathology
415-353-7248
___
I agree with Karen about a decent pay scale for California - $16.15 is a
ridiculous wage for California. Although San Francisco is on the high end
because of our insanely high cost of living (San Francisco even has it's own
minimum wage of $9.75/hr), $16.15 seems horribly low for anywhere in th
Hi everyone,
We are having a problem with a processing artifact that looks like very pale
staining in splotches just above the junction between the epidermis and dermis
but not extending all the way to the skin surface, and not everywhere at the
position. One of the processors had a clog in a
Hi,
We keep ours on by using egg albumin (from American Master Tech). Brush some
on the slide, let it air dry then pick up your sections. It will hold through
PASD as well as H&E.
Good luck!
Erin
PS A 1:4 Nair solution softens the block up nicely after you face it in.
Erin Martin, Histology
Good morning everyone,
We occasionally receive specimens that were fixed in alcohol but processed on
our machine, which starts in formalin. In our typical antigen retrieval we
either use a 95 degree waterbath for an hour or enzyme for 5 minutes. On
alcohol fixed tissues this chews up the tissu
Hi, Would anyone using SOX10 antibody please tell me where they buy it? If
you have a procedure that you would be willing to share as well I would be very
appreciative. Thank you!
Erin Martin
UCSF Dermatopathology
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We too were told by our internal safety compliance officer that 10% NBF has to
be stored in flammable cabinets and that is now how we store it. We were also
told that our general purpose household bleach has to be in a flammable
cabinet
Erin Martin
UCSF Dermatopathology
__
Hi everyone,
Are any of you using the Intellipath LIS? Not the Intellipath stainer from
Biocare. If so, I have some questions on how you use the procedures report to
get your orders.
Thanks!
Erin Martin
UCSF Dermatopathology
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Hi all,
>From the responses I have received, almost everyone loves their microwave
>processors for soft tissue biospies. Is anyone using a microwave on derm?
Erin
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Hi all,
What experiences have you all had with microwave processors? Sakura?
Milestone? We're trying to figure something our. I know there will be some
passionate responses...And I look forward to them!
Thanks so much,
Erin Martin, HT
___
Hist
Hi Jeanine,
What are spacer coils? I don't think I've ever heard of them.
Thanks,
Erin Martin
UCSF Dermatopathology
From: Bartlett, Jeanine (CDC/CCID/NCZVED) [mailto:j...@cdc.gov]
Sent: Mon 12/22/2008 11:29 AM
To: Martin, Erin; histonet
S
[mailto:m...@pathview.com]
Sent: Mon 12/22/2008 11:36 AM
To: Martin, Erin
Subject: RE: [Histonet] Slide drying
Erin, may I ask why your doctors want them filed so quickly?
Michael Mihalik
PathView Systems | cell: 214.733.7688 | 800.798.3540 | fax: 270.423.0968
-Original Message-
From:
Hello everyone,
I was asked to find out how to dry slides quickly. They are glass coverslipped
in an automated coverslipper at the reference lab we use and the our docs want
them filed in less than 12 hours from the time they are coverslipped. We have
been putting them in a 125 degree C con
Good morning,
Does anyone know of a source for antibody NGF p75 other than
Chemicon/Millipore? The last few lots we have gotten from them have been
dramatically weaker so I'd like to find a new vendor.
Thanks!
Erin
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