RE: Daily Digest, H. Pylori
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From: | "Clark, Susan" <SClark@mhs-net.com> |
To: | 'HistoNet Server' <histonet@pathology.swmed.edu> |
Reply-To: | |
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-----Original Message-----
From: HistoNet Server
[mailto:histonet@pathology.swmed.edu]
Sent: Wednesday, July 12, 2000 4:01 AM
To: HistoNet Server
Subject: Daily Digest
----------------------------------------------------------------------
Date: 11 Jul 2000 05:45:53 -0500
From: Lee & Peggy Wenk <lpwenk@mail.netquest.com>
Subject: Re: Fwd: NSH Scholarships and Starting a Histology
program
This is Peggy Wenk. I am the program director
of a HT and a HTL program at a hospital, and
I am giving a workshop at NSH on how to set
up a HT or HT school.
If anyone is interested in how to start a program,
please give me a call at 248/551-9079. (work)
PLEASE, only call me if you are REALLY interested
in starting a program. If you have some hospitals
and/or colleges SERIOUSLY interested in starting
a program. We need to talk for a LONG time,
and probably several times. But I can
give you some ideas on how to start. I have helped
other hospitals and colleges with ideas, and
try to come up with ideas that would work given
the hospitals and/or colleges involved (there is
no RIGHT way to set up a program. There are, on
the other hand, wrong ways.)
If you simply think a school is a good idea, or
something you can do in your "spare time" at
work, or because you have always wanted to teach,
or are just curious, please don't call. I don't
mean to sound rude, but these conversations do
take up a lot of my time (read hours), and as you
know, time is limited to everyone who works in a
hospital.
So, yes, I'm willing to to talk, but PLEASE,
don't all 1200+ histonetters try calling me
on this topic.
I have thought about giving this as a teleconference,
but am concerned that this is a really limited
topic with a very small audience. Maybe those who
are just curious, etc., could let me know if this
is a teleconference you would like to hear. Respond
via histonet or through my home email which is:
Lpwenk@netquest.com
Peggy A. Wenk, HTL(ASCP)
Schools of HIstotechnology
William Beaumont Hospital
Royal Oak, MI 48073
DENISE BLAND-PIONTEK wrote:
>
> Subject: NSH Scholarships and Starting a Histology program
> Date: Mon, 10 Jul 2000 18:01:29 -0600
> From: "DENISE BLAND-PIONTEK" <DBLANDP1@FAIRVIEW.ORG>
> To: <histonet@pathology.swmed.edu'>
>
> I'm asking these questions for a fellow histotechnologist,
Pam Buzzard, who
resides in Georgia. She will be joining the Histonet soon.
Does the NSH offer
any scholarships for attending nationals? Does anyone have a
suggested
curriculum with what each course should entail as far as
starting a histotech
program is concerned? She has been asked by a local college
to initiate a
program, but has little info to go on. I have already
suggested attending the
workshop that is going to be offered at Nationals this year.
I will inform her
of all answers posted on the histonet, but she can otherwise
be contacted at
PDBUZZ68@aol.com.
> Thank you,
> Denise Bland-Piontek HTL (ASCP)
> Fairview University Medical Center
> Minneapolis, MN
----------------------------------------------------------------------
Date: 11 Jul 2000 05:46:08 -0500
From: Lee & Peggy Wenk <lpwenk@mail.netquest.com>
Subject: how to unsubscribe for vacations
For those going on vacations, remember to
unsubscribe from histonet. Please don't set
your system to tell us you are on vacation.
At fifty messages a day, that can be
overwhelming to histonet.
Print this page out and save it. Or save
this page as a file on your computer
until you need it.
So, to unsubscribe:
1. Address email to histonet
histonet@pathology.swmed.edu
Do NOT piggy-back this on someone else's
message. It comes through with a "re:",
or a "forward", and you will not be
able to unsubscribe that way.
2. In the subject area, write
unsubscribe
Please note that there are 11 letters.
Make certain they are in the correct order.
Do NOT add any other words, like "please"
or "re:" or any quotation marks ("), or
any exclamation marks (!).
3. Hit Send or Transmit.
That should do it.
When you get back from vacation, and
want to rejoin Histonet,
1. Address an email to histonet at
histonet@pathology.swmed.edu
2. In the SUBJECT area, type
subscribe
again, no other words, no ",
9 letters in the right order, etc.
3. Hit send/transmit
You should be rejoined in a
few minutes to a few hours. Be
patient. If you haven't been rejoined
to histonet by the next day, try again.
Have fun and see you when you get back.
Peggy A. Wenk, HTL(ASCP)
William Beaumont Hospital
Royal Oak, MI 48073
----------------------------------------------------------------------
Date: 11 Jul 2000 07:44:18 -0500
From: "Coskran, Timothy M"
<timothy_m_coskran@groton.pfizer.com>
Subject: IHC on Liver
As many of the replies indicate, the problem could be due to
endogenous
biotin as well as endogenous peroxidase. We've found that
using one of the
available avidin-biotin blocking kits will help reduce the
background. You
could also change your detection from a standard ABC or LSAB
to the Envision
technique which avoid the use of biotin. We've used this
kit with a few
antibodies on liver sections with good success.
Good luck,
Tim Coskran
Pfizer
----------------------------------------------------------------------
Date: 11 Jul 2000 08:12:17 -0500
From: "Tom T. McNemar" <TMcNemar@lmhealth.org>
Subject: H. Pylori by IHC...
Does anyone have a good protocol for H. Pylori on the
Ventana ES? I have
tried a couple of different antibodies. Thanks for your
help.
Tom Mc Nemar
Pathology Supervisor
Licking Memorial Hospital
Newark, Ohio
I USE CELL MARQUE AB. THE PROTOCOL ON THE ES IS: ANTIGEN
RET. 25MINS IN CITRATE BUFFER, COOL 10 MINS, 32MIN INCUBATION AND AMPLIFY
----------------------------------------------------------------------
Date: 11 Jul 2000 08:12:32 -0500
From: Jerry Chi-Yuan Hu <ragnarok@ruf.rice.edu>
Subject: Slightly OT: Live cells anyone?
Hello Everyone,
I am looking for a way to isolate cells from thin slices (at
100 um
thick) and to start a cell line from these cells. Everyone
I've spoken to
says that the fresh tissue has to be embedded for slicing in
a microtome
cryostat, though slices of 100 um might crack... I also do
not know if
the embedding medium is going to kill my cells.
If anyone knows how to use the microtome (or cryotome) to
get thick slices
of live cells please let me know. Your help is greatly
appreciated!
Jerry Hu
----------------------------------------------------------------------
Date: 11 Jul 2000 08:12:53 -0500
From: dspjhd@cha.quebec.qc.ca
Subject: Please unsubscribe
----------------------------------------------------------------------
Date: 11 Jul 2000 08:13:07 -0500
From: dspjhd@cha.quebec.qc.ca
Subject: Please unsubscribe
----------------------------------------------------------------------
Date: 11 Jul 2000 08:13:32 -0500
From: Jenny Molde <ctsmolde@samiot.uct.ac.za>
Subject: Marker for T-cells in sheep
Dear Histonetters
I am looking for a lymphocyte marker for sheep. Anyone out
there had any
experience with this. Many thanks.
Jenny Molde
----------------------------------------------------------------------
Date: 11 Jul 2000 10:30:28 -0500
From: "Vicki Gauch" <GauchV@mail.amc.edu>
Subject: Re: consult charges, documentation
Kathy,
We also had this dilemma....we changed our procedure so
that now when the
physician calls to have a consult sent we fax him/her a
request form that has
a portion stating that he is requesting us to send slides to
(the name of the
physician we are sending to). The physician signs this form
and faxes it back
to us. We process the request, send the slides on their way
and we keep those
request forms on file. We used to accept a phone request
but now we require
that form to be filled out before we will even begin the
process. Hope this
helps...
Have a great day : )
Vicki
Albany Medical Center
>>> hkcormier <hkcorm@banet.net> 07/10/00 07:13PM >>>
Hello All,
I have an interesting question for you all, our corporate
compliance
program is currently looking at path consult charges...how
does everyone
(anyone) document physician requests for consults. By this I
mean the
patient's doctor calls the office and requests that the case
be sent out
to another pathologist, not the "house" pathologist sending
our for a
second opinion. Our issue is that we are a fairly small
hospital with
only 2 pathologist, our pathologists will routinely send out
cases for a
second opinion, on say bone marrows to the regions top bone
marrow guy.
The local visiting oncologist and ocasionally a local
surgeon - primary
care physician will request that a case be sent out, some
where else.
The issue is, is that it is usually a phone call from the
doctor or
doctor's staff and we never receive any written order or
request. This
our course would slow us all down and wreck havoc with our
customer
service policy. Our corporate people feel that without
documentation
from somewhere, this may be construed as fraud. Any ideas?
Any one ever
deal with this before? Any suggestions? Thanks! Kathy
----------------------------------------------------------------------
Date: 11 Jul 2000 10:31:05 -0500
From: "MacDonald, Jennifer" <jmacdonald@sach.org>
Subject: RE: consult charges, documentation
The order can be faxed to you. Attach the faxed order to
the report that
you keep filed. This way you have official documentation of
the request.
Tests can be initiated by a verbal order but must have a
written order on
file. Who pays for the consultation?
Jennifer MacDonald
> ----------
> From: hkcormier[SMTP:hkcorm@banet.net]
> Sent: Monday, July 10, 2000 6:13 PM
> To: histonet@pathology.swmed.edu
> Subject: consult charges, documentation
>
> Hello All,
> I have an interesting question for you all, our corporate
compliance
> program is currently looking at path consult charges...how
does everyone
> (anyone) document physician requests for consults. By this
I mean the
> patient's doctor calls the office and requests that the
case be sent out
> to another pathologist, not the "house" pathologist
sending our for a
> second opinion. Our issue is that we are a fairly small
hospital with
> only 2 pathologist, our pathologists will routinely send
out cases for a
> second opinion, on say bone marrows to the regions top
bone marrow guy.
> The local visiting oncologist and ocasionally a local
surgeon - primary
> care physician will request that a case be sent out, some
where else.
> The issue is, is that it is usually a phone call from the
doctor or
> doctor's staff and we never receive any written order or
request. This
> our course would slow us all down and wreck havoc with our
customer
> service policy. Our corporate people feel that without
documentation
> from somewhere, this may be construed as fraud. Any
ideas? Any one ever
> deal with this before? Any suggestions? Thanks! Kathy
>
>
----------------------------------------------------------------------
Date: 11 Jul 2000 10:31:19 -0500
From: "Tom T. McNemar" <TMcNemar@lmhealth.org>
Subject: RE: consult charges, documentation
Our path secretary handles all of the consult sendouts. We
never receive a
written request either and I suspect that it would do us no
good to request
one. The secretary maintains a log of what was sent, where
it was sent,
when, and who requested that it be sent. When they are
returned, she then
goes to her log and enters the date returned.
It has never been an issue here..... maybe no one thought of
it..... maybe
no one cares.......
I'll be watching the replies.
Tom Mc Nemar
Pathology Supervisor
Licking Memorial Hospital
Newark, Ohio
> -----Original Message-----
> From: hkcormier [SMTP:hkcorm@banet.net]
> Sent: Monday, July 10, 2000 7:14 PM
> To: histonet@pathology.swmed.edu
> Subject: consult charges, documentation
>
> Hello All,
> I have an interesting question for you all, our corporate
compliance
> program is currently looking at path consult charges...how
does everyone
> (anyone) document physician requests for consults. By this
I mean the
> patient's doctor calls the office and requests that the
case be sent out
> to another pathologist, not the "house" pathologist
sending our for a
> second opinion. Our issue is that we are a fairly small
hospital with
> only 2 pathologist, our pathologists will routinely send
out cases for a
> second opinion, on say bone marrows to the regions top
bone marrow guy.
> The local visiting oncologist and ocasionally a local
surgeon - primary
> care physician will request that a case be sent out, some
where else.
> The issue is, is that it is usually a phone call from the
doctor or
> doctor's staff and we never receive any written order or
request. This
> our course would slow us all down and wreck havoc with our
customer
> service policy. Our corporate people feel that without
documentation
> from somewhere, this may be construed as fraud. Any
ideas? Any one ever
> deal with this before? Any suggestions? Thanks! Kathy
>
----------------------------------------------------------------------
Date: 11 Jul 2000 10:31:53 -0500
From: Cynthia Favara <cfavara@niaid.nih.gov>
Subject: RE: Marker for T-cells in sheep
Try contacting Pam Dilbeck at WSU. I have not done t-cel
markers in sheep,
but have done in mice with success using Dako CD3 in murine
models. If you
would like more info let me know.
Cynthia Favara
NIAID/RML/LPVD
903 South 4th Street
Hamilton, MT 59840
PH: 406-363-9317
FAX: 406-363-9286
e-mail: CF98d@nih.gov <mailto:CF98d@nih.gov>
----------------------------------------------------------------------
Date: 11 Jul 2000 10:32:15 -0500
From: "Paul Howard Lockwood" <TigrSnke@ix.netcom.com>
Subject: Re: Mental illness: the other side
- -----BEGIN PGP SIGNED MESSAGE-----
Hash: SHA1
Dear Bryan,
My thoughts exactly. I appreciate your courage in
voicing them.
As for the comments made about a supervisor needing to
know the
mental state of their employees, I ask this question: At
what point
does caring for an employee become intrusive, and even
discriminatory?
A short seminar, or even a couple of semesters of Behavioral
Psychology does not qualify someone to make a diagnosis, or
any
judgement concerning a person's mental state. This is always
best left
to a professional with years of training, and an internship
under
their belt.
Sincerely,
Paul Howard Lockwood
- - -----Original Message-----
From: Bryan Llewellyn <bryand@netbistro.com>
To: Histonet <histonet@pathology.swmed.edu>
Date: Monday, July 10, 2000 1:00 AM
Subject: Mental illness: the other side
>> Lastly, if we screen out all of the mentally ill from
jobs, what
>> are we to do with them? They have rights, and one of them
is the
right
>> to pursue happiness by being gainfully employed.
>
>I too thought long and hard about whether I should reply to
the
postings on
>this subject. I finally decided that I should because I
can bring an
aspect
>to the discussion that has not yet been made. Please
excuse what may
appear
>to be bragging, but I am going to speak very frankly
because I have
found
>some off the comments made on this subject quite demeaning
and
insulting. I
>do not apologise for saying this. I think it needs to be
said.
>
>I am a long time chronic depressive. I have been depressed
on and
off
>(mostly on) for about 50 years (I am 57), and have been a
passive
suicide
>since I was about eight. The source of my emotional
problems is
abuse as a
>child; physical, sexual and emotional. Did you ever wonder
where
abused
>children went when they grew up? We hide among you.
>
>Depression is considered to be a mental illness. I am
therefore one
of
>those people you are all wondering whether you should fire
because
you are
>concerned I might attack you.
>
>I do my job, and rather well, I always thought. I am the
supervisor
of a
>small histology lab, and have been the supervisor of a very
large
histology
>lab years ago in Winnipeg. I qualified at the highest
possible
levels
>available at the time (1969 and 1979) in two countries
(Britain and
Canada).
>I authored and administered for several years three
separate
correspondence
>courses for the Canadian professional Society in advanced
histological
>techniques. I have written a few papers on histological
subjects
(amyloid
>staining, H&E substitutes). I set up the StainsFile web
page, and
have done
>all the work for it with the exception of one article. I
venture to
suggest
>that I have received considerable respect for my technical
abilities
over
>the years from coworkers and pathologists, some of whom
have been
quite
>demanding.
>
>I am politically active and have been asked on more than
one occasion
to run
>for office provincially. I have been declared an honorary
woman
because of
>my strong committment to gender equity. I feel just as
strongly
about
>racial equality and gay and lesbian issues. I venture to
suggest
that I
>have made a noticeable contribution to society.
>
>I have been married to Linda for 37 years. She has borne
the brunt
of my
>depression for all that time. We have three children, all
of whom
are well
>educated (Jason a city planner, Stevyn a pharmacist, and
David a
Ph.D.
>student in organo-metallic chemistry at McGill
unioversity). None of
them
>have inherited my depression. All of them love and respect
me and
will miss
>me when I die.
>
>Mentall illness is no more a single entity than any other
branch of
human
>activity. Both smallpox and the common cold are viral
diseases, but
why
>would anyone in their right mind think that a person with a
cold is
as
>dangerous as a person with smallpox. Please get a
perspective.
Mental
>illness ranges from the inocuous to the dangerous. Most
people alive
(that
>means you) have some kind of a neurosis, and all neuroses
are a form
of
>mental illness. From very personal experience, I can tell
you that
those
>who suffer most from mentall illnesses are the people with
it and
those who
>love them. An example is the poor progress of the
StainsFile web
site, on
>which I have been unable to work for a year.
>
>I am most certainly not ashamed of my mental state. In
fact, I am
quite
>proud of the fact that I have been strong willed enough to
rise above
my
>handicap. I think I have made a contribution to society.
I have
never hit
>anyone. I have never killed anyone. I treat others with
respect.
Why
>should I be discriminated against because someone else has
a hangup
(a
>neurosis) about emotional disorders? Why should I be fired
when it
is your
>problem? Would you fire me if I had one arm? Would you
refuse to
work with
>me if I stuttered? Would you send me to the back of the
bus if I
were
>black? Please tell me how discriminating against me
because of my
>depression is any different from those things.
>
>Remember, we are all innocent until proven guilty. Please
do not
fire me
>until I have done something worth being fired for. As for
not hiring
>someone because in a ten minute interview, an interviewer
with no
>psychiatric training decides the candidate is nuts, please,
get a
life!
>
>I would request that people think before they post comments
that are
>demeaning to those like me.
>
>Bryan Llewellyn
>Depressive, and absolutely NOT ashamed of it.
>
>
>
>
>
>
>
>
>
>
>
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----------------------------------------------------------------------
Date: 11 Jul 2000 10:32:41 -0500
From: jim <jim@proscitech.com.au>
Subject: RE: Slightly OT: Live cells anyone?
Easy. You need a Vibratome. These have a vibrating blade and
this means
cutting
can occur without compression. You can look at our online
pages, but we cannot
sell into the N American market.
Cheers
Jim Darley
ProSciTech Microscopy PLUS
PO Box 111, Thuringowa QLD 4817 Australia
Ph +61 7 4774 0370 Fax:+61 7 4789 2313
service@proscitech.com
Great microscopy catalogue, 500 Links, MSDS, User Notes
ABN: 99 724 136 560 www.proscitech.com
On Tuesday, July 11, 2000 10:53 PM, Jerry Chi-Yuan Hu
[SMTP:ragnarok@ruf.rice.edu] wrote:
>
> Hello Everyone,
>
> I am looking for a way to isolate cells from thin slices
(at 100 um
> thick) and to start a cell line from these cells.
Everyone I've spoken to
> says that the fresh tissue has to be embedded for slicing
in a microtome
> cryostat, though slices of 100 um might crack... I also
do not know if
> the embedding medium is going to kill my cells.
>
> If anyone knows how to use the microtome (or cryotome) to
get thick slices
> of live cells please let me know. Your help is greatly
appreciated!
>
> Jerry Hu
>
----------------------------------------------------------------------
Date: 11 Jul 2000 10:33:20 -0500
From: "Johnson, Mickey" <JohnsoM@shmc.org>
Subject: RE: Mental illness: the other side
Thank you all for your bravery! I salute you. Co-dependence
with a parent
short of physical abuse only catches a thin edge of what
physically abused
children experience. In addition, as is clear from this
thread of
correspondence, the experience has life long consequences
for the abused,
which never goes away. I am amazed and frankly disgusted
that our judicial
system does not recognize this fact and still releases level
3 sexual
offenders back to molest more children! We all need to apply
pressure on the
legislative and judicial systems when the opportunity
presents itself to
change this. Thanks for taking the time to read my
thoughts.
Best Regards.
Mickie
- -----Original Message-----
From: Thomas J. Kuwahara [mailto:tom@resolve3d.com]
Sent: Monday, July 10, 2000 10:02 AM
To: Bryan Llewellyn
Cc: Histonet
Subject: Re: Mental illness: the other side
Dear Bryan: I've been off a couple of weeks and it's been
quite a
morning reading all my 300+ emails but I have to salute your
bravery in
sending such a very personal and moving message over this
often
contentious internet site. If you ever want to come work
for a private
company in San Francisco, let me know. Regards, Tom
Bryan Llewellyn wrote:
>
> > Lastly, if we screen out all of the mentally ill from
jobs, what
> > are we to do with them? They have rights, and one of
them is the right
> > to pursue happiness by being gainfully employed.
>
> I too thought long and hard about whether I should reply
to the postings
on
> this subject. I finally decided that I should because I
can bring an
aspect
> to the discussion that has not yet been made. Please
excuse what may
appear
> to be bragging, but I am going to speak very frankly
because I have found
> some off the comments made on this subject quite demeaning
and insulting.
I
> do not apologise for saying this. I think it needs to be
said.
>
> I am a long time chronic depressive. I have been
depressed on and off
> (mostly on) for about 50 years (I am 57), and have been a
passive suicide
> since I was about eight. The source of my emotional
problems is abuse as
a
> child; physical, sexual and emotional. Did you ever
wonder where abused
> children went when they grew up? We hide among you.
>
> Depression is considered to be a mental illness. I am
therefore one of
> those people you are all wondering whether you should fire
because you are
> concerned I might attack you.
>
> I do my job, and rather well, I always thought. I am the
supervisor of a
> small histology lab, and have been the supervisor of a
very large
histology
> lab years ago in Winnipeg. I qualified at the highest
possible levels
> available at the time (1969 and 1979) in two countries
(Britain and
Canada).
> I authored and administered for several years three
separate
correspondence
> courses for the Canadian professional Society in advanced
histological
> techniques. I have written a few papers on histological
subjects (amyloid
> staining, H&E substitutes). I set up the StainsFile web
page, and have
done
> all the work for it with the exception of one article. I
venture to
suggest
> that I have received considerable respect for my technical
abilities over
> the years from coworkers and pathologists, some of whom
have been quite
> demanding.
>
> I am politically active and have been asked on more than
one occasion to
run
> for office provincially. I have been declared an honorary
woman because
of
> my strong committment to gender equity. I feel just as
strongly about
> racial equality and gay and lesbian issues. I venture to
suggest that I
> have made a noticeable contribution to society.
>
> I have been married to Linda for 37 years. She has borne
the brunt of my
> depression for all that time. We have three children, all
of whom are
well
> educated (Jason a city planner, Stevyn a pharmacist, and
David a Ph.D.
> student in organo-metallic chemistry at McGill
unioversity). None of them
> have inherited my depression. All of them love and
respect me and will
miss
> me when I die.
>
> Mentall illness is no more a single entity than any other
branch of human
> activity. Both smallpox and the common cold are viral
diseases, but why
> would anyone in their right mind think that a person with
a cold is as
> dangerous as a person with smallpox. Please get a
perspective. Mental
> illness ranges from the inocuous to the dangerous. Most
people alive
(that
> means you) have some kind of a neurosis, and all neuroses
are a form of
> mental illness. From very personal experience, I can tell
you that those
> who suffer most from mentall illnesses are the people with
it and those
who
> love them. An example is the poor progress of the
StainsFile web site, on
> which I have been unable to work for a year.
>
> I am most certainly not ashamed of my mental state. In
fact, I am quite
> proud of the fact that I have been strong willed enough to
rise above my
> handicap. I think I have made a contribution to society.
I have never
hit
> anyone. I have never killed anyone. I treat others with
respect. Why
> should I be discriminated against because someone else has
a hangup (a
> neurosis) about emotional disorders? Why should I be
fired when it is
your
> problem? Would you fire me if I had one arm? Would you
refuse to work
with
> me if I stuttered? Would you send me to the back of the
bus if I were
> black? Please tell me how discriminating against me
because of my
> depression is any different from those things.
>
> Remember, we are all innocent until proven guilty. Please
do not fire me
> until I have done something worth being fired for. As for
not hiring
> someone because in a ten minute interview, an interviewer
with no
> psychiatric training decides the candidate is nuts,
please, get a life!
>
> I would request that people think before they post
comments that are
> demeaning to those like me.
>
> Bryan Llewellyn
> Depressive, and absolutely NOT ashamed of it.
- --
Thomas J. Kuwahara - Senior Immunohistochemist
Resolution Sciences Corporation - http:www.resolve3d.com
3801 Sacramento St., Suite 621, San Francisco, CA 94118
T: 415/750-2307 F: 415/750-2332 E: tom@resolve3d.com
----------------------------------------------------------------------
Date: 11 Jul 2000 10:33:49 -0500
From: GSennello@nexstar.com
Subject: Re: Slightly OT: Live cells anyone?
You probably need to speak to someone about cell culture. I
have collected
induced tumors from mice (using sterile technique) with a
scalpel and then
placed them in a small amount of the appropriate tissue
culture media and
minced them into a slurry which was then put in a flask to
grow. Many cell
lines do very well. From your message I can't see where the
100 micron
slices comes into play ? Why? And yes I think most
embedding media would
kill cells although most cell lines can be frozen if done
properly.
Jerry
Chi-Yuan Hu To:
histonet@pathology.swmed.edu
<ragnarok@ruf cc:
.rice.edu> Subject:
Slightly OT: Live cells
anyone?
07/11/00
06:53 AM
Hello Everyone,
I am looking for a way to isolate cells from thin slices (at
100 um
thick) and to start a cell line from these cells. Everyone
I've spoken to
says that the fresh tissue has to be embedded for slicing in
a microtome
cryostat, though slices of 100 um might crack... I also do
not know if
the embedding medium is going to kill my cells.
If anyone knows how to use the microtome (or cryotome) to
get thick slices
of live cells please let me know. Your help is greatly
appreciated!
Jerry Hu
----------------------------------------------------------------------
Date: 11 Jul 2000 10:34:12 -0500
From: "Weems, Joyce" <JWEEMS@sjha.org>
Subject: RE: consult charges, documentation
We have a form that the drs. office faxes to us - with
physician signature,
that we use for this sort of thing.
Joyce Weems
Pathology Manager
Saint Joseph's Hospital of Atlanta
-----Original Message-----
From: hkcormier [SMTP:hkcorm@banet.net]
Sent: Monday, July 10, 2000 7:14 PM
To: histonet@pathology.swmed.edu
Subject: consult charges, documentation
Hello All,
I have an interesting question for you all, our
corporate compliance
program is currently looking at path consult
charges...how does
everyone
(anyone) document physician requests for consults.
By this I mean
the
patient's doctor calls the office and requests that
the case be sent
out
to another pathologist, not the "house" pathologist
sending our for
a
second opinion. Our issue is that we are a fairly
small hospital
with
only 2 pathologist, our pathologists will routinely
send out cases
for a
second opinion, on say bone marrows to the regions
top bone marrow
guy.
The local visiting oncologist and ocasionally a
local surgeon -
primary
care physician will request that a case be sent out,
some where
else.
The issue is, is that it is usually a phone call
from the doctor or
doctor's staff and we never receive any written
order or request.
This
our course would slow us all down and wreck havoc
with our customer
service policy. Our corporate people feel that
without documentation
from somewhere, this may be construed as fraud. Any
ideas? Any one
ever
deal with this before? Any suggestions? Thanks!
Kathy
----------------------------------------------------------------------
Date: 11 Jul 2000 15:22:02 -0500
From: Diane.Burica@advocatehealth.com (Diane Burica)
Subject: unssubscribe
----------------------------------------------------------------------
Date: 11 Jul 2000 15:54:23 -0500
From: Sheila Poellein <sheila_poellein@deaconess.com>
Subject: AP computer systems
We are a current Sunquest computer user looking for a new
system since they
will cease support of their AP product in the near future.
Our three top
choices are Copath, Tamtron, and SCC's Softpath. I would
appreciate any and
all comments of these three systems especially of the SCC
system of which we
are least familiar. If you are a user of any of these,
what do you
like/dislike about your system. Thanks in advance.
Sheila
----------------------------------------------------------------------
Date: 11 Jul 2000 15:54:39 -0500
From: "Bonnie P Whitaker" <Bonnie.P.Whitaker@uth.tmc.edu>
Subject: help with Syndecan-1, FA1, SDF1, NRG-1
Hi,
One of the pathologists that I am working with wants to do a
project
involving the following antibodies:
Syndecan-1
FA1 (fetal antigen1)
SDF1 (stromal cell-derived factor 1)
NRG-1 (neuregulins)
Doe anyone have any experience with these? If so, please
recommend sources
and share any tips for getting these to work.
Thanks,
Bonnie Whitaker
UT--Houston
----------------------------------------------------------------------
Date: 11 Jul 2000 15:54:54 -0500
From: Gayle Callis <uvsgc@msu.oscs.montana.edu>
Subject: Re: IH on Liver Tissue
There is a peroxidase quench that will block ALL forms of
peroxidase,
totally. This is the glucose oxidase method.
Hsu H-M, et al Am J Pathology 188:209-217,1984
Andrew SM and Jasani G Histchem J 19:426-430, 1987
Vector provided me with the exact protocol
>Date: Mon, 10 Jul 2000 14:43:03 -0400
>From: Jeff Crews <jcrews@organo.com>
>Subject: Re: IH on Liver Tissue
>To: kkdulany@unmc.edu, histonet@pathology.swmed.edu
>
> With extremely bloody tissue like spleen or liver, it
is sometimes
> impossible to quench all of the peroxidase present in
the blood. Try
> an alkaline-phoshatase detection system.
>
> Jeffrey Crews, HTL (ASCP)
> Organogenesis, Inc.
>
>
>______________________________ Reply Separator
_________________________________
>Subject: IH on Liver Tissue
>Author: <kkdulany@unmc.edu> at internet
>Date: 07/10/2000 11:03 AM
>
>
>How can you successfully perform immunohistochemistry on
slides of liver
>tissue using horse-radish peroxidase and DAB? How do you
quench the
>endogenous peroxidase in the tissue so everything doesn't
turn brown? I've
>tried 3, 10 and 15 % H2O2 in both methanol and di water for
20 min. up to 1
>hour with no success. The tissues are formalin fixed and
embeded in
>paraffin. We then used a pH 6.0 citrate buffer/microwave
antigen retrieval
>system for our primary Ab detection. Even with all that
the endogenous
>enzyme caused the false positive with the DAB. Anyone have
any
>suggestions?
>Thank you for all replies.
>Karen in Omaha
>
>
>
>
>
>
>
Gayle Callis
Veterinary Molecular Biology
Montana State University
Bozeman MT 59717-3610
406 994-4705
406 994-4303
----------------------------------------------------------------------
Date: 11 Jul 2000 15:55:27 -0500
From: Cynthia Favara <cfavara@niaid.nih.gov>
Subject: RE: Slightly OT: Live cells anyone?
Jerry,
You do not have to embedd to cut frozen sections. I
am presuming
[always dangerous] you are working with a piece of tissue.
Tissue can be
flash frozen in liguid nitrogen and can then be put on a
chuck for cutting.
It is possible to do this so the tissue remains frozen by
dipping the chuck
in liquid nitrogen and slowly building a little throne for
the tissue. Make
sure the tissue remains frozen as well. 100um pieces may
crack but since you
are going to isolate cells I would not think cracking would
matter.
Good Luck,
Cynthia Favara
NIAID/RML/LPVD
903 South 4th Street
Hamilton, MT 59840
PH: 406-363-9317
FAX: 406-363-9286
e-mail: CF98d@nih.gov <mailto:CF98d@nih.gov>
----------------------------------------------------------------------
Date: 11 Jul 2000 15:55:41 -0500
From: Cynthia Favara <cfavara@niaid.nih.gov>
Subject: RE: whole eye serial sections
I took a workshop from a group in Tennessee that had a
wonderful
presentation on eyes. I could probably find the name if you
desire.
Cynthia Favara
NIAID/RML/LPVD
903 South 4th Street
Hamilton, MT 59840
PH: 406-363-9317
FAX: 406-363-9286
e-mail: CF98d@nih.gov <mailto:CF98d@nih.gov>
----------------------------------------------------------------------
Date: 11 Jul 2000 15:55:59 -0500
From: Cynthia Favara <cfavara@niaid.nih.gov>
Subject: RE: IH on Liver Tissue
I do not know what species you are working with but I do IHC
with HRP on
murine liver all the time with no difficulty at all.
Sections are cut at 4um
and endogenous peroxidase is blocked for 15 minutes in 0.3%
vol/vol hydrogen
peroxide in PBS-0.02% Tween for 15 minutes.
Cynthia Favara
NIAID/RML/LPVD
903 South 4th Street
Hamilton, MT 59840
PH: 406-363-9317
FAX: 406-363-9286
e-mail: CF98d@nih.gov <mailto:CF98d@nih.gov>
----------------------------------------------------------------------
Date: 11 Jul 2000 15:56:15 -0500
From: Gayle Callis <uvsgc@msu.oscs.montana.edu>
Subject: Sheep antibodies
SeroTec at www.serotec.co.uk
Gayle Callis
Veterinary Molecular Biology
Montana State University
Bozeman MT 59717-3610
406 994-4705
406 994-4303
----------------------------------------------------------------------
Date: 11 Jul 2000 15:56:39 -0500
From: Nick_Madary@hgsi.com
Subject: Open until filled Histology position
Histology Position Available
Human Genome Sciences, Inc
Salary Position M-F some weekends
Must be proficient in the following areas:
Performing small animal necropsies and gross dissection,
All aspects of research veterinary histology(including
cryotomy)
Animal and Human Immunohistochemistry
Certification required
ISH experience and degree desirable
Send Resume to Human Genome Sciences, Inc
Human Resources Attn: Neubela Dahi
9410 Key West Ave
Rockville, Md 20850
In your cover letter mention this ad and reference Nick
Madary
For question regarding this position you may contact Nick
Madary via Email
at Nick_Madary@HGSI.COM or call 301 610 5790 ext 3537
----------------------------------------------------------------------
Date: 11 Jul 2000 15:57:05 -0500
From: "Gamble,Marilyn S" <Marilyn.S.Gamble@kp.org>
Subject: RE: NSH Scholarships and Starting a Histology
program
NSH Scholarships, for continuing education, are made
available through NSH,
and the gererous sponsorship of many of our vendor
companies. The criteria,
and deadline date, is established by the NSH Awards
Committee, for
nominees/applicants. The information is published annually
in "NSH In
Action" (sent to all NSH members). It is too late to apply
for this year's
awards, but I would encourage members to become more
involved in this
process. The percentage of members who apply and/or
nominate someone is
very low.
-----Original Message-----
From: DENISE BLAND-PIONTEK
[SMTP:DBLANDP1@FAIRVIEW.ORG]
Sent: Monday, July 10, 2000 5:01 PM
To: histonet@pathology.swmed.edu
Subject: NSH Scholarships and Starting a
Histology program
I'm asking these questions for a fellow
histotechnologist, Pam
Buzzard, who resides in Georgia. She will be joining the
Histonet soon. Does
the NSH offer any scholarships for attending nationals? Does
anyone have a
suggested curriculum with what each course should entail as
far as starting
a histotech program is concerned? She has been asked by a
local college to
initiate a program, but has little info to go on. I have
already suggested
attending the workshop that is going to be offered at
Nationals this year. I
will inform her of all answers posted on the histonet, but
she can otherwise
be contacted at PDBUZZ68@aol.com.
Thank you,
Denise Bland-Piontek HTL (ASCP)
Fairview University Medical Center
Minneapolis, MN
----------------------------------------------------------------------
Date: 11 Jul 2000 15:57:33 -0500
From: "Pam M. Dilbeck" <pmd@vetmed.wsu.edu>
Subject: Re: Marker for T-cells in sheep
Jenny--I have run Dako's CD3 A452 on several different
species (canine,
feline, equine, etc) but never tried on ovines. You might
try it--run a
lymph node as a control tissue. I use citrate buffer with
steam for
antigen retrieval and incuabate overnight in refrig. (use at
1:50,000). I
use Signet's ultra streptavidin (USA) detection and AEC for
the
chromogen. Let me know if you would like more information.
Pam
On Tue, 11 Jul 2000, Jenny Molde wrote:
> Dear Histonetters
> I am looking for a lymphocyte marker for sheep. Anyone out
there had any
> experience with this. Many thanks.
>
> Jenny Molde
>
>
>
>
Pam Dilbeck
Immunohistochemistry Section
Washington Animal Disease Diagnostic Laboratory
----------------------------------------------------------------------
Date: 11 Jul 2000 15:57:51 -0500
From: "Ronnie Houston" <wee_rory@hotmail.com>
Subject: non-histology topics
Please get back to what Histonet was set up for - an
exchange of matters
related to Histotechnology.
The recent discussions, lamblastings and character
assassinations have no
place on Histonet.
Sure, people have rights to express their feelings, but
Histonet is not the
correct avenue for this.
I highly commend Brian's stance and courage, and if people
had the common
sense to limit Histonet topics to Histology, he would not
have been forced
to make the painful decision to put forward publicly his
Let's keep the list histo-related from now on to avoid this
unpleasant and
unnecessary situation arising again.
Ronnie Houston
Cytochemistry & Molecular Pathology
Texas Scottish Rite Hospital for Children
2222 Welborn Street
Dallas, TX 75219
(214) 559 7744
(214) 559 7768 - fax
rhouston@tsrh.org
________________________________________________________________________
Get Your Private, Free E-mail from MSN Hotmail at
http://www.hotmail.com
----------------------------------------------------------------------
Date: 11 Jul 2000 15:58:07 -0500
From: "Gamble,Marilyn S" <Marilyn.S.Gamble@kp.org>
Subject: More Than A Gut Feeling
As part of the management workshop that I taught for several
years, I, also,
utilized the "More Than a Gut Feeling" information. Once you
have
established your hiring criteria, It teaches you how to
develop questions,
interview, and to obtain reponses that will give you insight
into past
behaviors (attitudes, interpersonal skills, dealing with
problems, etc.) and
performance. Past behavior/performance responses can
predict future
behaviors/performance.
It is not a "screen" for mental illness, nor would
eliminate a good
employee from being hired into the workplace.
-----Original Message-----
From: Janice Mahoney [SMTP:JMAHONEY@alegent.org]
Sent: Monday, July 10, 2000 11:15 AM
To: bryand@netbistro.com;
histonet@pathology.swmed.edu;
tom@resolve3d.com
Subject: Re: Mental illness: the other side
-Reply
I don't believe any part of Vinnie's workshop goes
into determining
if a person has a mental illness. What it does go into is
whether a job
candidate has the correct personaloity traits to work in the
sometimes
highly stresssful field of Histology. Not every person
posssesses the
ability to "fit in" in our labs. We usually have to have
the ability to
work as a team, communicate effectively, make critical
decisions, work under
stress, be self motivated etc., etc.
As far a having the potential for violence, there
are some
indicators and situations that may make the probability
increase.
Discrimination is not the issue. Supervisors need to be
aware of an
employees emotional state as well as their work. Its no
different than
being aware of an employee who is having personal poroblems
that cause them
to make errors in thier technical work. A supervisor should
be just as
aware of an employees mental state that may cause him/her to
injur or become
injured.
Jan Mahoney
----------------------------------------------------------------------
Date: 11 Jul 2000 15:58:22 -0500
From: Medilex123@aol.com
Subject: Re: Foetuses
Carmen,
I know we have to be concerned about the feling of grieving
parents but I
would feel a little concerned about dressing up a fixed
fetus, on the grounds
of health and safety as well as the aesthetic look of a
fetus after
fixation.
When I worked in a maternity hospital in the UK, parents who
lost babies and
fetuses didn't have to ask whether they could have a photo
or not, a polaroid
was routinely taken by the nursing/midwifery staff along
with a foot-print
which was placed onto a small piece of card with the babies
name on it. They
were offered the photo and print if they wanted it.
Regards,
Glyn Woodward
----------------------------------------------------------------------
Date: 11 Jul 2000 15:58:48 -0500
From: Dana Settembre <settembr@UMDNJ.EDU>
Subject: Re: Immunos on Cytology Specimens
On Thu, 6 Jul 2000 DRitter@stmarygj.com wrote:
> I would appreciate any feed back on Immunohisto procedures
done on
> cytology smears,.cytospins etc.
> We recently purchased a Biogenex Optimax Immuno stainer
(and love it).
> I heard that you could fix smears etc. in cold acetone and
then start
> your normal run procedure. Has any one used anything else
and had great
> results?
> Thanks
> Deb Ritter, HT ASCP
> St. Marys Hosp.
> Grand Junction, Colorado
>
Hello Deb,
When I run cytology smears I start them at buffer and join
them with my
regular paraffins at the H2O2 step.
When I get them, usually I get them in water, I put them in
buffer. In
the mean time my paraffins are deparaffinzing to water and
getting
pretreated as necessary and go into buffer and H2O2 with the
smears.
Dana Settembre
Immunohistochemistry Lab
Pathology Department
University Hospital
Newark, New Jersey
USA
----------------------------------------------------------------------
Date: 11 Jul 2000 15:59:07 -0500
From: Dana Settembre <settembr@UMDNJ.EDU>
Subject: Re: IH on Liver Tissue
On Mon, 10 Jul 2000 kkdulany@unmc.edu wrote:
> How can you successfully perform immunohistochemistry on
slides of liver
> tissue using horse-radish peroxidase and DAB? How do you
quench the
> endogenous peroxidase in the tissue so everything doesn't
turn brown? I've
> tried 3, 10 and 15 % H2O2 in both methanol and di water
for 20 min. up to 1
> hour with no success. The tissues are formalin fixed and
embeded in
> paraffin. We then used a pH 6.0 citrate buffer/microwave
antigen retrieval
> system for our primary Ab detection. Even with all that
the endogenous
> enzyme caused the false positive with the DAB. Anyone
have any
> suggestions?
> Thank you for all replies.
> Karen in Omaha
>
>
Karen,
What antibody are you using? Everythin you do sounds like
what I do but
maybe you can skip the antigen retrieval step and see what
happens. My
guess is that omitting that will help.
Dana Settembre
Immunohistochemistry Lab
Pathology Department
University Hospital
Newark, New Jersey
USA
----------------------------------------------------------------------
Date: 11 Jul 2000 15:59:39 -0500
From: "Jennings-Siena, Debbie"
<ds.jennings-siena@baylordallas.edu>
Subject: RE: consult charges, documentation
Just wanted to let everyone know that on June 21,2000 the
American Society
of Clinical Pathologists hosted a consensus conference on
second opinions in
diagnostic anatomic pathology. Ten panelist from around the
country,
including eight pathologists of various disciplines, a
patient represenative
and a surgeon met in Washington D.C. to debate the who,
what, how and when
of second opinions in ap. They felt that it was important
to determine when
second opinion review of Anatomic pathology slides is
warranted for patient
care. The consensus conference is part of the ASCP Patient
Safety
Initiative, which was created in response to a report on
medical errors
released late last year by the Institute of Medicine. The
Panelists debated
which patients need second opinions, which diagnoses need
more frequent
review, and cost and payment issues. The proceedings of the
conference are
expected to be published in an upcoming issue of the
American Journal of
Clinical Pathology and on the ASCP web site (www.ASCP.org).
This was reported in the Washington Report, Dated July 5,
2000. I hope that
when this information is published that it will be helpful,
although not a
total answer to your question.
Debbie J. Siena
NSH Legislative Chairperson
Baylor University Medical Center
Dallas, TX 75246
- -----Original Message-----
From: hkcormier [mailto:hkcorm@banet.net]
Sent: Monday, July 10, 2000 6:14 PM
To: histonet@pathology.swmed.edu
Subject: consult charges, documentation
Hello All,
I have an interesting question for you all, our corporate
compliance
program is currently looking at path consult charges...how
does everyone
(anyone) document physician requests for consults. By this I
mean the
patient's doctor calls the office and requests that the case
be sent out
to another pathologist, not the "house" pathologist sending
our for a
second opinion. Our issue is that we are a fairly small
hospital with
only 2 pathologist, our pathologists will routinely send out
cases for a
second opinion, on say bone marrows to the regions top bone
marrow guy.
The local visiting oncologist and ocasionally a local
surgeon - primary
care physician will request that a case be sent out, some
where else.
The issue is, is that it is usually a phone call from the
doctor or
doctor's staff and we never receive any written order or
request. This
our course would slow us all down and wreck havoc with our
customer
service policy. Our corporate people feel that without
documentation
from somewhere, this may be construed as fraud. Any ideas?
Any one ever
deal with this before? Any suggestions? Thanks! Kathy
----------------------------------------------------------------------
Date: 11 Jul 2000 16:00:16 -0500
From: "Colbert, Laurie" <LColbert@phsca.org>
Subject: Cat Scratch Controls
Does anyone know where I can purchase cat scratch controls?
Thanks in
advance!
Laurie Colbert
Providence Saint Joseph Med Ctr
Burbank, CA 91505
----------------------------------------------------------------------
Date: 11 Jul 2000 16:00:56 -0500
From: "Goodwin, Diana" <DGoodwin@CHSNJ.org>
Subject: RE: Alcian Blue for ... [urban myths]
Gentlemen:
After reading through your e-mail threads, I hurried
back to my
ancient storage closet where I keep solid reagents
now, since
ready made
solutions became available. Lo and behold, what do
I find but a
dusty jar
of Alcian Blue 8GX!
Jim, please let me know when the price reaches that
of gold!
Diana Goodwin, HT
Trenton, NJ
> ----------
> From: Mark Ray[SMTP:darkdaym@earthlink.net]
> Sent: Friday, July 07, 2000 2:47 PM
> To: jim; J. A. Kiernan
> Cc: Histonet
> Subject: RE: Alcian Blue for ... [urban myths]
>
> John,
>
> I was not quite correct in saying that Aldrich had sold
out their last
> batch of Alcian Blue 8GX. At the present moment they have
1x5g and
> 1x25g
> cat no 236551 in stock. When we attempted to purchase a
> manufacturing
> quantity this spring, they told us that it was
unavailable. I guess
> they
> still had some small packages, but it looks bleak for the
present.
> Hopefully the pyridine derivative will become generally
available.
>
> Mark Ray
> EK Industries
>
>
> > [Original Message]
> > From: J. A. Kiernan <jkiernan@julian.uwo.ca>
> > To: jim <jim@proscitech.com.au>
> > Cc: Histonet <Histonet@pathology.swmed.edu>
> > Date: 7/7/00 1:30:20 AM
> > Subject: RE: Alcian Blue for ... [urban myths]
> >
> > On Thu, 6 Jul 2000, Jim Darley wrote:
> >
> > > Here is the note from our wholesaler/ manufacturer:
> > >
> > > "Thank you for your E Mail concerning Alcian Blue 8GX.
As per
> previous
> > > correspondence the problem is with us and will not
disappear.
> > > The last 3 years we found some old ICI material (low
dye content
> 10-20%), which
> > > we upgraded. That has come to an end; no company in
the world to
> our
> knowledge
> > > is producing the material, textile quality or stains
quality. ..."
> >
> > > ... a 1996 CD ROM will not reveal anything that has
happened
> during
> > > the past three years.
> >
> > That's true; I don't have the 1999 version of the C.I.
CD-ROM.
> > However, on May 11th 1999 the Biol Stain Commission
certified a
> > batch of alcian blue 8GX for the Aldrich Chemical
Company. See
> > Biotech. & Histochem. 74 (5) p. 274 (Sept 1999). So
there must
> > have been some new stuff around last year.
> >
> > Alcian blue 8GX (dye content approx 50%) is in the
Sigma
> > and Aldrich catalogues for 2000-2001; same price as
> > haematoxylin. (Curiously, both dyes are about $10
cheaper for
> > 25 grams if you buy from Sigma rather than Aldrich.
Strange,
> > when they're the same company! In the Fluka catalogue
for
> > 1999-2000 - also the same firm, I think - the prices
of both
> > dyes are some $20 higher than Aldrich's.) Aldrich also
supply
> > a "pyridine variant" of alcian blue, which is more
expensive,
> > and in the past they sold another variant called
"alcec blue,"
> > which could also be used for the same staining methods
(see
> > F. Green 1991: The Sigma-Aldrich Handbook of Stains,
Dyes and
> > Indicators, p. 69-72).
> >
> > A low dye content such as the 10-20% in your old ICI
material
> > is not necessarily a bad thing for alcian blue, and
batches
> > with high dye content (70% +) often perform badly. It
seems
> > likely that the additives (dextrin, boric acid etc)
are
> > needed in adequate amount.
> >
> > John A. Kiernan,
> > Department of Anatomy & Cell Biology,
> > The University of Western Ontario,
> > LONDON, Canada N6A 5C1
> >
> >
> >
>
>
>
> --- Mark Ray
> --- darkdaym@earthlink.net
> --- EarthLink: It's your Internet.
>
>
>
----------------------------------------------------------------------
Date: 11 Jul 2000 16:01:44 -0500
From: Maria Mejia <maria@mail.ski.org>
Subject: RE: whole eye serial sections
thank you for responding, but the lab with the rabbit whole
eyes
found a lab to do the work in Bay Area.
regards
maria mejia
----------------------------------------------------------------------
Date: 11 Jul 2000 16:02:03 -0500
From: Maria Mejia <maria@mail.ski.org>
Subject: whole eye serial sections
I would like to thank very much all those individuals that
responded
to my message on serial sections of rabbit whole eyes. The
lab
that is need of this work has found a lab to do it. Again, I
thank everyone on the histonet.
regards
Maria Mejia
Smith-Kettlewell Eye Res. Inst.
S.F. CA
----------------------------------------------------------------------
Date: 11 Jul 2000 16:04:50 -0500
From: kkdulany@unmc.edu
Subject: IH on Liver Tissue-- Thank you all
I think this histonet is the best idea yet for continuing
education. In
response to my question about excessive background staining,
you wonderful
people took your time to help. I had 14 replies in the
first hour after
I wrote and today I had 10 more. Thank you all so much. I
had not
considered biotin staining as my problem as I am rather new
at some of
these stains but I have already order a new kit to block the
biotin.
Previously I had stained lots of slides but mostly it was
on pancreas
tissue using insulin, glucagon, somatastatin, and
pancreatic poly peptide
and these did not need any pre- treatment or digestions.
Thank you all.
Karen in Omaha
----------------------------------------------------------------------
Date: 11 Jul 2000 16:05:27 -0500
From: DELONG_CYNTHIA_A@LILLY.COM
Subject: Zinc Formalin vs 4% Paraformaldehyde
Hello everyone,
I have a fixation question regarding saline perfused brains.
What is the
difference in drop fixing brains in zinc formalin vs 4%
Parafomaldehyde?
Or is there? These are then cryo protected and froze in
liquid
nitrogen. It seems as though zinc produces the same
results. Are certain
antigens harder to retrieve?
Just curious
Cindy
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