etc..
Since this is a new concept for me I am reaching out to see if anyone in
this group has worked with PEG and can give me references, diorection,
protocols...
As always, thanks in advance~.
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
Jackson Hall, Room 2-155
321 Church St
with
the agar it will not have [processed properly. I was never able to salvage
those samples. It took me a couple times to figure out the solution.
Just a thought.
Colleen Forster HT(ASCP)QIHC
On Fri, May 17, 2024 at 2:32 PM Jay Lundgren via Histonet <
histonet@lists.utsouthwestern.edu>
if
interested in more information.
Colleen Forster HT(ASCP)QIHC
cfors...@umn.edu
On Wed, May 8, 2024 at 9:56 AM Charles Riley via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Awesome thank you Val. I like the multi control option. Can save money in
> the end by using l
for that. I am fortunate to have a second processor I can use for special
programs and not hold up my main runs.
Colleen Forster HT(ASCP)QIHC
University of Minnesota
BLS Histology and IHC Laboratory
On Thu, Mar 28, 2024 at 9:15 AM Paula Sicurello via Histonet <
histonet@lists.utsouthwestern.
I agree. Making some of these simple solutions that need to be FRESH is the
better way to go. As John said, there are ma ny books with these formulas
in them.
I have used Davidson's for different projects and I make mine in the lab
fresh each time tissue is harvested.
Colleen Forster HT(ASCP
You are very welcome!
Colleen
On Tue, Nov 7, 2023 at 4:02 PM Naira Margaryan
wrote:
> Awesome, thank you so much Colleen, for such quick response,
> Naira
>
> On Tue, Nov 7, 2023 at 4:01 PM Colleen Forster wrote:
>
>> Naira,
>>
>> Contact Lee Dickey with Ted
Naira,
Contact Lee Dickey with Ted Pella. They carry the whole line of large block
adapters for the Leica microtomes.
lee_dic...@tedpella.com
I have this set up and it works great.
Colleen Forster HT(ASCP)QIHC
On Tue, Nov 7, 2023 at 3:58 PM Naira Margaryan via Histonet <
histo
I would love too but unable to move the whole family!
Colleen Forster
On Fri, Oct 27, 2023 at 11:20 AM Stephanie L. Thompson via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Come to beautiful New Hampshire, the best beaches, Great White Mountains,
> no income or state ta
Even 30um is too thick for the routine IHC on glass. You will never
penetrate the whole thickness for staining.
Colleen Forster HT(ASCP)QIHC
On Fri, Aug 4, 2023 at 2:05 PM Alonso Martínez Canabal <
acana...@ciencias.unam.mx> wrote:
> Hi, thank you for your reply.
> I cannot do m
Alonso,
For sections that thick you would collect them as you always have, stain
them as floating sections and then mount onto a glass slide. The routine
standard methods for IHC will never penetrate a 50um thick section.
Colleen Forster HT(ASCP)QIHC
On Fri, Aug 4, 2023 at 1:17 PM Alonso
I run a research lab with automated staining and truthfully,I make my
dilutions fresh for each run because proteins are so different in their
stability.
Colleen Forster HT(ASCP)QIHC
On Sun, Jul 2, 2023 at 7:08 PM Tony Henwood via Histonet <
histonet@lists.utsouthwestern.edu>
for comparison.
I am aware of the many variables. For better comparison to my lab we use
formalin and xylenes not a substitute.
Any and all infirnation will be includedThank you very much in advance.
Respectfully,
Colleen Forster
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
In my experience if the antibody are designed for flow they rarely work on
tissue samples.
Colleen Forster HT(ASCP)QIHC
University of MN
On Wed, Aug 24, 2022 at 1:56 PM Charles Riley via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> I have been given an antibody that is used
Donna,
I know first hand, if you have any computer issues that take out your
software, ( power surge for example) Leica does NOT reinstall the program.
You are left to find a different program. It took us a long time to get a
program so we could use both the IPC/IPS again. The new software isn't
some of you share what you have and the pros/cons?
I need to start the search for the replacement I would like.
Thank you in advance.
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
Jackson Hall, Room 2-155
321 Church St. SE
Minneapolis, MN 55455
612-626-1930
ith specific
> cryo attachments is used.
>
> Sincerely,
>
> Paula Sicurello
>
> Sent from my iPhone
>
> > On May 18, 2022, at 12:55 PM, Colleen Forster via Histonet <
> histonet@lists.utsouthwestern.edu> wrote:
> >
> > FollowingI am in r
FollowingI am in research and I have never cut this cold.
Colleen Forster
On Wed, May 18, 2022 at 2:04 PM Ken Marzinsky via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Can anyone tell me why research labs often require cryostat cutting head
> temperatures down to -
Great advice Tim. I still do this 30 years later. It definitely expands
your scope of work, keeps the job interesting and builds your resource
network
Colleen Forster HT(ASCP)QIHC
On Mon, May 9, 2022, 5:38 PM Tim Morken via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Pa
Make sure the periodic acid is made fresh EACH time you run the stain.
That can also make a big difference in the stain quality.
Colleen Forster HT(ASCP)QIHC
On Thu, Sep 23, 2021 at 6:14 PM Tony Henwood (SCHN) via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> I agree w
I agree with Terri. I also have an 1850 and will use it until parts are no
longer available which could be,. like she said, years. We also have a
local company do the PM and repairs and will use it until
it absolutely cannot be repaired.
Colleen Forster HT(ASCP)QIHC
University of Minnesota
BLS
I'd love to join you but I will be working that entire day
Colleen Forster
On Wed, May 19, 2021 at 3:24 PM Lauren Sweeney via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi Everyone,
>
> It is not too late to join us for the GSH Virtual Summit on May 22, 2021
>
Wow, what an excellent list John. I didn't ask the question but will surely
use the response. Thank you for sharing.
Respectfully,
Colleen Forster HT(ASCP)QIHC
University of Minnesota
On Mon, May 3, 2021 at 12:32 PM John Kiernan via Histonet <
histonet@lists.utsouthwestern.edu>
t;map" and then that goes with the block. It works well.
Colleen Forster
On Thu, Apr 8, 2021 at 12:30 PM Cheryl via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi everyone-
> We have a researcher who needs to put multiple samples in one block for
> quality and cost control.
Hello Histonet,
Can you give me feedback on trying to do IHC on samples fixed in Zamboni's
fixative? I have an idea but need confirmation .
Thank you in advance
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
Jackson Hall, Room 2-155
321 Church St. SE
Minneapolis, MN 55455
612
,
Colleen Forster
On Mon, Jan 25, 2021 at 11:26 AM Tyrone Genade via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hello,
>
>
> On Saturday, January 23, 2021 1:00 PM, <
> histonet-requ...@lists.utsouthwestern.edu> wrote:
>
> > In my lab, water und
kit back into 4 degrees.
Just one thought.
Colleen Forster HT(ASCP)QIHC
U of MN
On Thu, Oct 22, 2020 at 2:30 PM Rhonda McCormick via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> I thought I'd reach out and see if anyone can help with some IHC
> troubleshooting (or know
have
used them can share.
Thank you in advance.
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
Jackson Hall, Room 2-155
612-626-1930
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Totally following this one...
And what do you use to record humidity and what would be the cut off for
good staining , especially for IHC stains.
Colleen Forster
On Wed, Aug 19, 2020 at 6:30 PM Patti Nelson via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hello Histo pe
info/histonet
>
>
>
> ___
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> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
B173 PWB 612-626-1930
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The Biocare certain was called the Nemesis. They are phasibg them out but
might be willing to come assist you.
Colleen Forster
On Thu, Oct 24, 2019, 2:43 PM Eileen Akemi Allison via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Ask Biocare or Dako. Unbeknownst to most of t
out of business. Can anyone confirm
> or deny this?
>
> Thanks.
> Sent using the mail.com
> mail app
> ___
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> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
&
Wow John,
Great information.,always so much to learn!~
Thank you,
Colleen Forster
U of MN
On Tue, Sep 10, 2019 at 10:55 AM Morken, Timothy via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> John, we love it when you "ramble!" It gives us an appreciatio
results.
Respectfully,
Colleen Forster HT(ASCP)
U of MN
On Sun, Sep 8, 2019, 10:36 AM John Garratt via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> The best I can offer is to advise you to wipe the knife holder area down
> with a cleaning solvent and use a fresh blade. C
I agree with Brett.
I believe the histological aspect will be horrible and probably not worth
the time and money spent. I feel you would be terribly disappointed with
the lack of usable results.
Colleen Forster HT(ASCP)QIHC
On Thu, Aug 22, 2019 at 11:14 AM Brett Connolly via Histonet <
histo
Biocare Medical Promark series are also great animal polymer based
detection that work very well.
https://biocare.net/products/detection/
Colleen Forster HT(ASCP)WQIUC
U of MN
On Wed, Jun 12, 2019 at 10:42 AM Paula Keene Pierce via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
&g
utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
B173 PWB 612-626-1930
*If submitting histology request please also forward to Lori Holm at
ho...@umn.edu *
__
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
B173 PWB 612-626-1930
*
Anatomic Pathology Manager *
>
> (914) 302-8424
> *ap...@cmmedical.com*
>
>
>
> *From:* Colleen Forster [mailto:cfors...@umn.edu]
> *Sent:* Thursday, February 21, 2019 11:59 AM
> *To:* Perl , Alison
> *Cc:* Melissa Owens; histonet@lists.utsouthwestern.edu
>
Wow...this is just crazy~ The regulations leave histology in a real tough
spot...
Feeling for all of you and yes, for the future histology techs coming up~
Colleen Forster
U of MN
On Thu, Feb 21, 2019 at 10:52 AM Perl , Alison via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
Yes! Your expertise is such a valuable resource..
C
On Wednesday, February 13, 2019, Bob Richmond wrote:
> You're welcome!
>
> I sat down and read through most of it as soon as I saw it. So glad John
> Kiernan's back!
>
>
> On Wed, Feb 13, 2019 at 8:48 PM C
THis looks likje a great resource...I will take time to look it over.
Thank you for all your valuable mentorship over 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:
> Joh
; Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
--
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
B173 PWB 612-626-1930
*If submitting histology request please also forward to Lori
Hello Dave,
I still do a lot of manual work and I also use Biocare reagents. They work
well and their customer service is very good.
Colleen Forster
On Fri, Jan 18, 2019 at 12:58 PM Jeanine Ronkowski via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi Dave:Our lab has used
.
Colleen Forster HT(ASCP)QIHC
U of MN
On Thu, Aug 30, 2018 at 12:58 PM, Jennifer Kempf via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Biocare Medical Intellipath...its completely open and is a continuous load
> machine, meaning you can start a run on one rack while still loadin
This sounds wonderful..I wish I were in a position to swoop it up!
Colleen Forster HT(ASCP)QIHC
On Wed, Jun 6, 2018 at 9:24 AM, Arrington, Karla A via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hello All,
>
> I hope everyone is enjoying the early part of summer.
&
On Tue, May 1, 2018 at 12:07 PM, shultz11 via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
>
> Leica equipment is now being made in China not Germany. I wish I would
> have known this before purchasing equipment.
> Kendra ShultzSent from my Verizon, Samsung Galaxy smartphone
>
To do samples that you suspect prion disease also needs to be done in a
lab specifically designed for that.
I agree, formalin is sufficient.,
Colleen
On Mon, Apr 23, 2018 at 11:14 AM, Rene J Buesa via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> I believe that is an extreme and
Following...would like to see the answer.
Colleen Forster
On Tue, Mar 27, 2018 at 3:25 PM, Karl Koessler via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Does anyone know of a stain or marker I can use to differentiate
> sympathetic from parasympathetic in sacral spinal c
I agree Terry,
The TMA slide is a very economical and powerful way to validate with
minimal slides needed.
Colleen Forster
On Tue, Mar 20, 2018 at 12:54 PM, Terri Braud via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Just another note: You can order unstained tissue mi
?
Thank you in advance!~
Respectfully,
Colleen Forster
U of MN
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you in advance!
Respectfully and hopeful,
Colleen Forster
U of MN
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Can anyone give me a processing schedule for Drosophila flies...very tiny.
Thank you in advance!
Colleen Forster HT(ASCP)QIHC
U of MN
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to
work with them..
Respectfully,
Colleen Forster HT(ASCP)QIHC
BLS Histology and IHC Laboratory
University of Minnesota
612-626-1930
On Thu, Jan 11, 2018 at 3:27 PM, Jennifer MacDonald via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Thank you to all that responded. I have a li
ichard*
>
>
>
> *From:* Colleen Forster [mailto:cfors...@umn.edu]
> *Sent:* Wednesday, December 27, 2017 4:23 PM
> *To:* Cartun, Richard
> *Cc:* histonet@lists.utsouthwestern.edu
> *Subject:* Re: [Histonet] Beta-Amyloid antibody for IHC
>
>
>
> CAUTION: This ema
Do you knot want to use 6E10 anymore? I believe you can still get it from
Biolegends?
https://www.biolegend.com/en-us/products/purified-anti-beta-amyloid--1-16-antibody-11228
Respectfully,
Colleen Forster HT(ASCP)QIHC
*University of Minnesota*
On Wed, Dec 27, 2017 at 3:20 PM, Cartun, Richard
gt;
>
> On Tuesday, December 19, 2017 9:45 AM, Colleen Forster via Histonet <
> histonet@lists.utsouthwestern.edu> wrote:
>
>
> Be sure you are processing them on an overnight process. Even if the
> samples are small it takes that time to process the agar properly.
>
>
ould think agar might be the same.
Just a thought,
Colleen Forster HT(ASCP)QIHC
U of MN
On Tue, Dec 19, 2017 at 11:29 AM, Liz Chlipala via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> I would try histogel instead of agar.
>
> Liz
>
> Elizabeth A. Chlipala, BS, HTL
I am following, would love to see the responses.
Colleen Forster
On Thu, Sep 28, 2017 at 5:14 PM, Judi Ford via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi Everyone,
> I am interested in connecting with techs/managers who are working in or
> have developed a tran
Cristi,
I follow the general guidelines of good fixation for the msajority. IF I am
testing something that has specific in the clinicla lab, I try it the same
on animal tissues for the same thing.
Colleen Forster HT(ASCP)QIHC
On Thu, Jun 15, 2017 at 4:05 PM, Eddie Martin via Histonet
Following.
Colleen Forster
On Mon, May 29, 2017 at 10:04 AM, Gregoire, Rhonda (AGR) via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Does anyone have any experience processing and paraffin embedding
> butterflies?
>
> Rhonda Gregoire, MLT
> Superviso
Thanks Gaylethis is the system the pathologist wanted to
but$3000.00 and he had no money
I want to try and work with more reasonably priced ideas first.not sure
I will ever get this one downI think Ill have better luck with bugs!
I will watch this video and read the notes
This sounds like a wonderful opportunity.I wish I were in a position to
go for it!
C
On Mon, Aug 15, 2016 at 12:43 PM, Lila Adams via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Good afternoon everyone,
> I thought I would post this job opportunity.
> CV Path Institute Job
Brett,
Are you interested in sending all mof them as a complete (-7 issues) set?
Colleen Forster
U of MN
On Tue, Aug 9, 2016 at 8:57 AM, Connolly, Brett M via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> HI all,
>
> Is anyone interested in old issues of JOH? My c
it at 1:400, citrate retrieval, 1 hour primary incubation. I use the
Rabbit on Rodent polymer from Biocare.
Respectfully,
'
Colleen Forster
On Tue, Jun 21, 2016 at 10:53 AM, Connolly, Brett M via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Liz,
> As long as it detects mouse
I find the same as Caroline Miller, about 20-25% with formalin fixation and
routine processing.
C
On Mon, Feb 22, 2016 at 3:41 PM, Caroline Miller via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> hi All, I have done some experiments in this area for mouse brains, and I
> find that
This looks wonderful!
Be sure to keep me on your list Pam so I can consider this meeting!
C
On Thu, Jan 28, 2016 at 2:50 PM, Pamela Marcum via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
>
>
> Good Afternoon,
>
>
>
>
> We would like to invite all of you to Branson Missouri for the
I think that is about average for good Tshirts these days.
C
On Tue, Jan 26, 2016 at 2:43 PM, Bitting, Angela K. via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Is it me or does anyone else think $20 is a lot of money for a T-shirt?
> The Histotechnology Professionals Day T-shirts on
I am interested to see what you hear BrettI need to do these same
markers and am not having good luck in FFPEfrozens , great...FFPE NOT!
C
On Tue, Nov 3, 2015 at 7:32 AM, Connolly, Brett M via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi all,
> I have a project that will be
I'd be very interested in this as well...could you shaere Karen.
Thanks.
C
On Mon, Nov 2, 2015 at 11:43 AM, Karen Cai via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> HELP:
>
>
>
> Hi,
>
> Is there anybody can provide me the price list/structure of the custom IHC
> services?
>
>
>
So very sorry to hear of Peggy's passing. She was such as inspiration to us
all. She will be greatly missed. May God grant her family the peace and
grace to pass into the following days with strength.
She will now be soaring with the eagles watching over everyone.
Rest in peace Peggy,
Colleen
I totally agree with William. I do animal IHC and I am, using the
Biocare Nemesis, which be the same as the Dako platform. Completely open
so you can do what you need to at a cost you can afford
Colleen Forster HT(ASCP)QIHC
u of MN
On 1/23/2014 11:44 AM, Will Chappell wrote:
Doing ihc
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Exactly Jennifer!
C
On 9/10/2013 6:32 PM, Jennifer MacDonald wrote:
As long as we do not need certification, licensure and minium education
requirements we will not be recognized as Laboratory Professionals.
From: Marcum, Pamela A pamar...@uams.edu
To: 'joelle weaver'
and in the human
tonsil the stain is great.
Any suggestions..
Thanks in advance!
Colleen Forster
U of MN
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I am interested in the answer as I use this same technique on my rodent
samples and have not had this issue.
On 7/2/2013 8:07 AM, Connolly, Brett M wro
Histonetters -
We had some rat tissues that were removed at necropsy and immediately fixed in
formalin for 48 hrs. Since the tissues
To all the histonetters,
IS anyone doing CD200 staining in FFPE mouse samples with good results?
If so, please share your information.
Thanks in advance...your help is always appreciated!!
Colleen Forster
U of MN
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What are you guys using as your primary for BrDU these days?
Thanks!
Colleen Forster
U of MN
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Does anyone have access to this reference for me? I have a person looking to ID
eosinophils in fat samples.
I am looking for a stain that will make finding them easierthis reference
was mentionedany other suggestions? These are FFPE samples.
Suggested Ref ex. LIllie 4th Ed. pp750.
!!
Colleen Forster
U of MN
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Hello everyone,
Can you please share with me the EGFR primary antibody you use and what
pretreatment you use with itthanks in advance!!
Colleen Forster
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Me too!!!
C
On 11/6/2012 3:44 PM, Bell, Pat wrote:
Hello to Everyone!! :)
Has anyone worked up CD11b in human tissue? We have tried one from Novus and
one from Serotec with no staining or staining that was not specific. I would
appreciate any help anyone could give! :)
Thank you,
Pat
Pat
Well said Toysha.
I don't think they have even really incorporated IHC into the histology
programs and that IS a routine technique now. We cannot promote in a
field what we do not teach!
Colleen Forster HT(ASCP)QIHC
U of MN
On 9/18/2012 12:06 PM, Mayer,Toysha N wrote:
Being in HTL
I second Patsy! I have used this antibody with both AP and DAB and have
had excellent results.
Colleen Forster
U of MN
On 9/13/2012 2:05 PM, Patsy Ruegg wrote:
By far the best ab for endothelial cells in mouse tissue is rat anti CD31
from Dianovo, it picks up the really early forming
Try Dako, they have a nice little slide printer out there now.
Colleen Forster
U of MN
On 8/15/2012 10:25 AM, Bell, Pat wrote:
I also have the slide-mate and have a lot of problems with the printing. We
also have to spend a lot of time rewriting and labeling them. I have been told
processor. I am interested in
procedures with and without the use of a hydrometer.
Thanks in advance!!
Colleen Forster
U of MN
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in human gut and yes, I have
done it on most major organs of the mouse.
Colleen Forster
U of MN
On 8/8/2012 10:38 AM, Eva Permaul wrote:
Just to clarify. Are you using it on mouse tissues? I am only asking
because the Thermo Scientific/Labvision/Neomarkers data sheet says it has
only been
Thanks Jan, that would be the same one I have and it works great!
Colleen Forster
U of MN
On 8/6/2012 2:59 PM, Jan Shivers wrote:
We have had success with Lab Vision's rabbit polyclonal on mouse tissue
(catalog # RB-9043), utilizing HIER for antigen retrieval.
Jan Shivers
U of MN Vet Diag
do this it will save you a LOT of headache.
Colleen Forster
U of MN
On 8/6/2012 3:57 PM, Colleen Forster wrote:
Thanks Jan, that would be the same one I have and it works great!
Colleen Forster
U of MN
On 8/6/2012 2:59 PM, Jan Shivers wrote:
We have had success with Lab Vision's rabbit
of them into one
big block?
Thanks in advance!!
Colleen Forster
Bionet Histology Laboratory
U of MN, AHC
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Hello Histoland,
Can anyone who may have used or is using this piece of equipment give me
their feed back? We are considering it to do an online dewaxing and
retrievel with the Biocare Nemesis stainer. Thanks in advacne for your
comments!
Colleen Forster HT(ASCP)QIHC
U of MN
Lab
I am wondering if any of you have ever used a Fast Green counter stain
in place of the Nuclear Fast Red? If so, what timing did you use?
Thanks,
Colleen Forster
U of MN
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http
Hello Histonetters,
I am looking for a CD31 that has been proven to work well in rat tissue
samples...have any of you out there done this with success? I have good
human and mouse antibodies not rat!
Thanks in advance!
Colleen Forster
Bionet Histology Research Laboratory
U of MN
612-626
for the autoradiography of diffusible
compounds by W.E. Stumpf. This volume is from 1976 so it goes way back!!
HELP!! anyone. Our medical library does not have this book and to get it
on Amazon was $172, too steep for my pocket.
Thanks
Colleen Forster HT(ASCP)QIHC
U of MN
Has anyone out in histo and been able to get good Cyclin D2 staining
in FFPE samples? If so, please share.
Thanks,
Colleen Forster
U of MN
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And if you have their coverslipper, it doesn't like the rounded edges
either!!
Colleen Forster.
Cheryl Crowder wrote:
Igor - We have a Leica slide labeler. It is easy to use, but we have found
that you should use slides with 90 degree corners and a rough surface.
Slides with clipped
* MUM-1
Thanks in advance...
Colleen Forster HT(ASCP)QIHC
Bionet Histology Service
U of MN
612-626-1930
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Biocare has a great CD31 for mouse and rat too. You do need the kit and
their primary but you can use formalin fixed samples with great results!
Colleen Forster
U of MN
Amy Porter wrote:
BD Biosciences has a great rodent CD31 for mouse and rat - however you
need to use their Zinc Fixative
To Ron Martinhistology IS BOTH A PROFESSION AND A
CAREER! You need a new job!
Colleen Forster HT(ASCP)QIHC
Wahlberg, Nikki wrote:
I would just like to add that in my opinion it is people who make statements like the one below that are holding our field back from being seen
I disagree. I do heat retrieval on frozen sections that have been fixed
in a formalin fix. If you use the correct protocol you can get very nice
IHC on these.
Colleen Forster HT(ASCP)QIHC
Anatomic Pathology Research Laboratory
U of MN
Johnson, Teri wrote:
In response to this thread
Animal brain is the same. IF you aior dry overnight and then into the
oven before starting your stains you will not lose sections.
Colleen Forster
U of MN
Barbara Albert wrote:
We've found this also. Even 30-60 minutes air drying helps alot with human
brain. We use regular slides and NBF
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