Hi everyone,
I am new to the forum. I am working on coral tissues embedded in
Immunobed resin and paraffin. We would like to stain both with H&E
and Azure II /Basic Fuchsin. I have never tried staining plastic with
H&E. Any suggestions or comments would be great! Since corals have a
calcium carbonate skeleton, the tissues were decalcified in a EDTA
solution.
Laura Hunt
UTA
On Feb 5, 2008, at 8:07 PM, histonet-request@lists.utsouthwestern.edu
wrote:
> Send Histonet mailing list submissions to
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>
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> When replying, please edit your Subject line so it is more specific
> than "Re: Contents of Histonet digest..."
>
>
> Today's Topics:
>
> 1. EpoR antibody (Colleen Forster)
> 2. RE: sections falling off (Debrosse-Serra, Beatrice)
> 3. Re: sections falling off (Rene J Buesa)
> 4. Re: Alcian Blue Quality Control OT (Robert Richmond)
> 5. HP staining (Martin, Gary)
> 6. Slide printers (ink) (Kim Merriam)
> 7. RE: Slide printers (ink) (Charles, Roger)
> 8. RE: Slide printers (ink) (Weems, Joyce)
> 9. Immunoperoxidase Double staining protocol (Reuel Cornelia)
> 10. Re: Slide printers (ink) (Patti Loykasek)
> 11. RE: Storage codes (Christine Tambasco)
> 12. Re: Slide printers (ink) (pkromund@gundluth.org)
> 13. Re: Immunoperoxidase Double staining protocol (Rene J Buesa)
> 14. thanks for the support and good wishes (Sebree Linda A.)
> 15. (no subject) (Margaryan, Naira)
> 16. Do mice have tonsils?? (Colleen Forster)
> 17. eosinophils on frozen section (Breisch, Eric)
> 18. RE: eosinophils on frozen section (Ingles Claire)
> 19. A gentle reminder about using subject line Re: [Histonet] (no
> subject) (Gayle Callis)
> 20. RE: eosinophils on frozen section (Weems, Joyce)
> 21. Re: Do mice have tonsils?? (Gayle Callis)
> 22. Re: eosinophils on frozen section (Gayle Callis)
> 23. RE: eosinophils on frozen section (Julia Dahl)
>
>
> ----------------------------------------------------------------------
>
> Message: 1
> Date: Tue, 05 Feb 2008 12:20:37 -0600
> From: Colleen Forster
> Subject: [Histonet] EpoR antibody
> To: histonet@lists.utsouthwestern.edu
> Message-ID: <47A8A8F5.3090606@umn.edu>
> Content-Type: text/plain; charset=ISO-8859-1; format=flowed
>
> Hello histonetters,
>
> Is anyone doing the EpoR antibody on FFPE for IHC? If so, could you
> share the vendor and a starting dilution.....thanks.
>
> Colleen Forster
> U of MN
>
>
>
> ------------------------------
>
> Message: 2
> Date: Tue, 5 Feb 2008 10:30:10 -0800
> From: "Debrosse-Serra, Beatrice"
> Subject: RE: [Histonet] sections falling off
> To: "Olek Michalski" , "Histonet"
>
> Message-ID:
>
> <8404DFBED5207B4B8E5EEF4332CEEA5305BD4C99@lajamrexm01.amer.pfizer.com>
> Content-Type: text/plain; charset="us-ascii"
>
> Try Newcomers silane coated slides. They are not cheap, but the
> sections
> stay on very well.
>
> Beatrice DeBrosse-Serra
> Pathology Scientist
> Pfizer Global Research & Development
> CB4, 2150
> 10646 Science Center Drive
> San Diego, CA 92121
> Phone# 858-622-5986
> Fax# 858-678-8290
>
>
>
> -----Original Message-----
> From: histonet-bounces@lists.utsouthwestern.edu
> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Olek
> Michalski
> Sent: Tuesday, February 05, 2008 10:00 AM
> To: Histonet
> Subject: [Histonet] sections falling off
>
>
> Dear Histonetters,
>
> a friend of mine just faced a massive sections falling off. She is
> doing
>
> Nissl staining in mouse brain (brains perfused with formalin,
> postfixed
> 3
> days, and cryosectioned) on poly-L-lysined slides. She just managed to
> pass trough xylene and decreasing grades of alcohol to water and the
> sections started to detach. We were trying to reattach them but it
> went
>
> out that sections are not flat any more. It seems like the tissue is
> rehydrated unevenly, but keeping it in water for hours didn't work. Is
> there any way to spread these sections not damaging them at the same
> time?
> She is likely to rescue this sections even if some work is needed.
>
> Best regards
> Olek Michalski
> --
> Laboratory of Neurobiology
> of Development and Evolution
>
> Nencki Institute of Experimental Biology
> ul. Pasteura 3, 02-093 Warszawa, Poland
> Tel. +48 22 5892268, Fax +48 22 8225342
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
> ------------------------------
>
> Message: 3
> Date: Tue, 5 Feb 2008 10:30:54 -0800 (PST)
> From: Rene J Buesa
> Subject: Re: [Histonet] sections falling off
> To: Olek Michalski , Histonet
>
> Message-ID: <87465.99172.qm@web61214.mail.yahoo.com>
> Content-Type: text/plain; charset=iso-8859-1
>
> If they were cryosectioned she did not have to go through xylene or
> graded alcohols to "dewax and hydrate" since there was no
> dehydration or wax infiltration to begin with.
>
> Cryosectioned sections just need to wash away the medium used to
> cryosection (OCT perhaps?) and just stain with the aqueous solutions.
>
> Later they can de dehydrated and cleared if a permanent mount is
> desired.
> Try to float the sections in a water bath and pick them up and
> don't try again to use xylene or alcohols.
> Probably she was following a procedure for paraffin embedded tissue
> that should have been adapted to frozen sections and it was not.
> René J.
>
> Olek Michalski wrote:
>
> Dear Histonetters,
>
> a friend of mine just faced a massive sections falling off. She is
> doing
> Nissl staining in mouse brain (brains perfused with formalin,
> postfixed 3
> days, and cryosectioned) on poly-L-lysined slides. She just managed to
> pass trough xylene and decreasing grades of alcohol to water and the
> sections started to detach. We were trying to reattach them but it
> went
> out that sections are not flat any more. It seems like the tissue is
> rehydrated unevenly, but keeping it in water for hours didn't work. Is
> there any way to spread these sections not damaging them at the same
> time?
> She is likely to rescue this sections even if some work is needed.
>
> Best regards
> Olek Michalski
> --
> Laboratory of Neurobiology
> of Development and Evolution
>
> Nencki Institute of Experimental Biology
> ul. Pasteura 3, 02-093 Warszawa, Poland
> Tel. +48 22 5892268, Fax +48 22 8225342
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
> ---------------------------------
> Looking for last minute shopping deals? Find them fast with Yahoo!
> Search.
>
> ------------------------------
>
> Message: 4
> Date: Tue, 5 Feb 2008 13:45:34 -0500
> From: "Robert Richmond"
> Subject: [Histonet] Re: Alcian Blue Quality Control OT
> To: histonet@lists.utsouthwestern.edu
> Message-ID:
>
> Content-Type: text/plain; charset=ISO-8859-1
>
> Claire Ingles remarks: So that's what GOP means!
>
> Not this grumpy old pathologist - I voted for Barack Obama!
>
> Bob Richmond
> Samurai Pathologist
> Knoxville TN
>
>
>
> ------------------------------
>
> Message: 5
> Date: Tue, 5 Feb 2008 11:00:57 -0800
> From: "Martin, Gary"
> Subject: [Histonet] HP staining
> To:
> Message-ID:
> <6ED9D4252F278841A0593D3D788AF24C01ACDF72@mailsvr.MARSHMED.local>
> Content-Type: text/plain; charset="us-ascii"
>
> To all who responded to my e-mail concerning rapid HP staining to
> include a yellow back ground ... thank you very much ... my question
> was
> answered.
>
> Gray
>
>
>
> ------------------------------
>
> Message: 6
> Date: Tue, 5 Feb 2008 11:48:08 -0800 (PST)
> From: Kim Merriam
> Subject: [Histonet] Slide printers (ink)
> To: Histonet
> Message-ID: <813260.30617.qm@web50306.mail.re2.yahoo.com>
> Content-Type: text/plain; charset=iso-8859-1
>
> Hi everyone,
>
> I was wondering what everyone's experience was with the TBS slide
> printer (Shurmark-plus), the one that prints with ink? I would
> appreciate input, good or bad.
>
> We currently have an etcher, and we hate it, so we are looking to
> trade it in for something that uses ink. I have used the Leica
> printer in the past and have had reasonably good luck with it, but I
> was wondering about the printer from TBS, I don't know anyone that
> has one.
>
> Kim
>
>
> Kim Merriam, MA, HT(ASCP)
> Cambridge, MA
>
> ---------------------------------
> Be a better friend, newshound, and know-it-all with Yahoo! Mobile.
> Try it now.
>
> ------------------------------
>
> Message: 7
> Date: Tue, 5 Feb 2008 14:58:42 -0500
> From: "Charles, Roger"
> Subject: RE: [Histonet] Slide printers (ink)
> To: "Kim Merriam"
> Cc: histonet@lists.utsouthwestern.edu
> Message-ID:
> <12E4E17FEF6EBE4BAE95BEB3CDCB57000943BB6E@enhbgpri04.backup>
> Content-Type: text/plain; charset="US-ASCII"
>
> Hello,
> Recently we bought a sakura slide writer that uses ink to print. The
> only problem I have found with the ink is if you put labels over the
> print and then try to remove the label to verify a number error, or
> something like that, the ink will actually come off with the label.
> If
> you can read upside down you can still verify the number. I did run
> this ink thru a battery of chemicals including straight formic acid
> for
> 5 minutes and the ink did not leave the slide. I would caution in
> buying a Sakura slide write as it has a very unfriendly Access based
> program and the writer does not work with charged slides. This has
> been
> verified by me and an independent engineer sent to look at this issue.
> I do use a TBS cassette writer and love that so if I can get my sakura
> sent back I will be looking at TBS's slide writer too.
> Good luck
> Roger
>
> Roger Charles
> Microbiologist
> Pennsylvania Veterinary Laboratory
> 2305 N Cameron St
> Harrisburg, PA 17110
> 717-787-8808
>
> -----Original Message-----
> From: histonet-bounces@lists.utsouthwestern.edu
> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Kim
> Merriam
> Sent: Tuesday, February 05, 2008 2:48 PM
> To: Histonet
> Subject: [Histonet] Slide printers (ink)
>
> Hi everyone,
>
> I was wondering what everyone's experience was with the TBS slide
> printer (Shurmark-plus), the one that prints with ink? I would
> appreciate input, good or bad.
>
> We currently have an etcher, and we hate it, so we are looking to
> trade it in for something that uses ink. I have used the Leica
> printer
> in the past and have had reasonably good luck with it, but I was
> wondering about the printer from TBS, I don't know anyone that has
> one.
>
> Kim
>
>
> Kim Merriam, MA, HT(ASCP)
> Cambridge, MA
>
> ---------------------------------
> Be a better friend, newshound, and know-it-all with Yahoo! Mobile.
> Try
> it now.
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
> ------------------------------
>
> Message: 8
> Date: Tue, 5 Feb 2008 15:25:58 -0500
> From: "Weems, Joyce"
> Subject: RE: [Histonet] Slide printers (ink)
> To: "Charles, Roger" , "Kim Merriam"
>
> Cc: histonet@lists.utsouthwestern.edu
> Message-ID:
> <1CD6831EB9B26D45B0A3EAA79F7EBD320518E54D@sjhaexc02.sjha.org>
> Content-Type: text/plain; charset="us-ascii"
>
> We have Sakura cassette and slide writers. We print charged slides
> daily.
>
> -----Original Message-----
> From: histonet-bounces@lists.utsouthwestern.edu
> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of
> Charles,
> Roger
> Sent: Tuesday, February 05, 2008 2:59 PM
> To: Kim Merriam
> Cc: histonet@lists.utsouthwestern.edu
> Subject: RE: [Histonet] Slide printers (ink)
>
> Hello,
> Recently we bought a sakura slide writer that uses ink to print. The
> only problem I have found with the ink is if you put labels over the
> print and then try to remove the label to verify a number error, or
> something like that, the ink will actually come off with the label.
> If
> you can read upside down you can still verify the number. I did run
> this ink thru a battery of chemicals including straight formic acid
> for
> 5 minutes and the ink did not leave the slide. I would caution in
> buying a Sakura slide write as it has a very unfriendly Access based
> program and the writer does not work with charged slides. This has
> been
> verified by me and an independent engineer sent to look at this issue.
> I do use a TBS cassette writer and love that so if I can get my sakura
> sent back I will be looking at TBS's slide writer too.
> Good luck
> Roger
>
> Roger Charles
> Microbiologist
> Pennsylvania Veterinary Laboratory
> 2305 N Cameron St
> Harrisburg, PA 17110
> 717-787-8808
>
> -----Original Message-----
> From: histonet-bounces@lists.utsouthwestern.edu
> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Kim
> Merriam
> Sent: Tuesday, February 05, 2008 2:48 PM
> To: Histonet
> Subject: [Histonet] Slide printers (ink)
>
> Hi everyone,
>
> I was wondering what everyone's experience was with the TBS slide
> printer (Shurmark-plus), the one that prints with ink? I would
> appreciate input, good or bad.
>
> We currently have an etcher, and we hate it, so we are looking to
> trade it in for something that uses ink. I have used the Leica
> printer
> in the past and have had reasonably good luck with it, but I was
> wondering about the printer from TBS, I don't know anyone that has
> one.
>
> Kim
>
>
> Kim Merriam, MA, HT(ASCP)
> Cambridge, MA
>
> ---------------------------------
> Be a better friend, newshound, and know-it-all with Yahoo! Mobile.
> Try
> it now.
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
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> may be privileged and is confidential information intended for the
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> recipient nor the employee or agent responsible for delivering this
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> If you have received this communication in error, please notify us
> immediately by replying to the message and deleting it from your
> computer. Thank you. Saint Joseph's Health System, Inc.
>
>
>
> ------------------------------
>
> Message: 9
> Date: Tue, 05 Feb 2008 14:34:27 -0600
> From: "Reuel Cornelia"
> Subject: [Histonet] Immunoperoxidase Double staining protocol
> To:
> Message-ID: <47A873F3020000C50002ADF9@nwcl02.tsrh.org>
> Content-Type: text/plain; charset=US-ASCII
>
> I was asked to do an immunoperoxidase double staining on CD61 ,Cd42,
> pf4 with an unknown mouse antibody that will work on platelets. Can
> somebody help me or any protocol available that I can refer to. I am
> used of IF double stianing but not Immunoperoxidase. Thank you.
>
> Reuel Cornelia, BS MT, AMT
> Cellular Pathology
> Texas Scottish Rite Hospital for Children
> 2222 Welborn Street
> Dallas, TX 75219
> Tel: 214-559-7766
> fax: 214-559-7768
>
> *******************************************************************************************************************
> Texas Scottish Rite Hospital for Children is one of the nation's
> leading pediatric centers for the
> treatment of orthopedic conditions, certain related neurological
> disorders and learning disorders,
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> We appreciate your efforts to protect the children's confidential
> information.
> *******************************************************************************************************************
>
>
>
>
>
> ------------------------------
>
> Message: 10
> Date: Tue, 05 Feb 2008 12:39:50 -0800
> From: Patti Loykasek
> Subject: Re: [Histonet] Slide printers (ink)
> To: "Charles, Roger" , Kim Merriam
>
> Cc: histonet@lists.utsouthwestern.edu
> Message-ID:
> Content-Type: text/plain; charset="US-ASCII"
>
> Roger- We have been using a sakura slide printer for a couple of
> years. I do
> agree with your comments about the software - not user friendly at
> all nor
> is it intuitive. I have used Access database in the past without these
> issues. I do not know about the labels, I don't think we've had that
> issue.
> Maybe it varies with the label. I don't quite understand your
> comment on
> charged slides, as all of the slides we put thru the printer are
> charged and
> we have no issues with that. We use charged slides (Okando Plus)
> from BBC
> and Probe-On Plus slides from ThermoFisher. What brand of slides
> were you
> using & what issue did you have with the slide printer from the usage?
>
>
> Patti Loykasek BS, HTL, QIHC
> PhenoPath Laboratories
> Seattle, WA
>
>
>
>
>
>
>
>> Hello,
>> Recently we bought a sakura slide writer that uses ink to print. The
>> only problem I have found with the ink is if you put labels over the
>> print and then try to remove the label to verify a number error, or
>> something like that, the ink will actually come off with the
>> label. If
>> you can read upside down you can still verify the number. I did run
>> this ink thru a battery of chemicals including straight formic acid
>> for
>> 5 minutes and the ink did not leave the slide. I would caution in
>> buying a Sakura slide write as it has a very unfriendly Access based
>> program and the writer does not work with charged slides. This has
>> been
>> verified by me and an independent engineer sent to look at this
>> issue.
>> I do use a TBS cassette writer and love that so if I can get my
>> sakura
>> sent back I will be looking at TBS's slide writer too.
>> Good luck
>> Roger
>>
>> Roger Charles
>> Microbiologist
>> Pennsylvania Veterinary Laboratory
>> 2305 N Cameron St
>> Harrisburg, PA 17110
>> 717-787-8808
>>
>> -----Original Message-----
>> From: histonet-bounces@lists.utsouthwestern.edu
>> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Kim
>> Merriam
>> Sent: Tuesday, February 05, 2008 2:48 PM
>> To: Histonet
>> Subject: [Histonet] Slide printers (ink)
>>
>> Hi everyone,
>>
>> I was wondering what everyone's experience was with the TBS slide
>> printer (Shurmark-plus), the one that prints with ink? I would
>> appreciate input, good or bad.
>>
>> We currently have an etcher, and we hate it, so we are looking to
>> trade it in for something that uses ink. I have used the Leica
>> printer
>> in the past and have had reasonably good luck with it, but I was
>> wondering about the printer from TBS, I don't know anyone that has
>> one.
>>
>> Kim
>>
>>
>> Kim Merriam, MA, HT(ASCP)
>> Cambridge, MA
>>
>> ---------------------------------
>> Be a better friend, newshound, and know-it-all with Yahoo! Mobile.
>> Try
>> it now.
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>>
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>>
>
>
>
> This e-mail message, including any attachments, is for the sole use
> of the
> intended recipients and may contain privileged information. Any
> unauthorized
> review, use, disclosure or distribution is prohibited. If you are
> not the intended
> recipient, please contact the sender by e-mail and destroy all
> copies of the
> original message, or you may call PhenoPath Laboratories, Seattle,
> WA U.S.A.
> at (206) 374-9000.
>
>
>
>
> ------------------------------
>
> Message: 11
> Date: Tue, 5 Feb 2008 21:10:37 +0000
> From: Christine Tambasco
> Subject: RE: [Histonet] Storage codes
> To: Barbara Albert , histonet
>
> Message-ID:
> Content-Type: text/plain; charset="iso-8859-1"
>
>
> I always kept my gold chloride in the refrigerator. Yours is in a
> vial though so is it a powder?
> That is what I used to have I kept at room temperature.
> Just my advice.
> Christine Tambasco, HT (ASCP)
> St. Marys Hospital
> Amsterdam, NY> Date: Mon, 4 Feb 2008 15:33:30 -0800> From: barbaraaalbert@yahoo.com
> > To: histonet@lists.utsouthwestern.edu> Subject: [Histonet] Storage
> codes> > Hi all,> I just received some vials of Gold Chloride that I
> had ordered and was checking the label for stoarge requirements. It
> has "Storage Code White". I haven't heard of storage codes and want
> to know where I can go to find out what they mean.> > Thanks,>
> Barbara Albert> UCSF Medical Center> San Francisco> > >
> ---------------------------------> Never miss a thing. Make Yahoo
> your homepage.> _______________________________________________>
> Histonet mailing list> Histonet@lists.utsouthwestern.edu> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
> _________________________________________________________________
> Climb to the top of the charts! Play the word scramble challenge
> with star power.
> http://club.live.com/star_shuffle.aspx?icid=starshuffle_wlmailtextlink_jan
>
> ------------------------------
>
> Message: 12
> Date: Tue, 5 Feb 2008 15:34:42 -0600
> From: pkromund@gundluth.org
> Subject: Re: [Histonet] Slide printers (ink)
> To: Patti Loykasek
> Cc: histonet@lists.utsouthwestern.edu,
> histonet-bounces@lists.utsouthwestern.edu, "Charles, Roger"
>
> Message-ID:
> >
>
> Content-Type: text/plain; charset=US-ASCII
>
> Do any of these slide printers affect precut control tissue on the
> charged
> slides?
> Pamela
>
>
>
> Patti Loykasek
>
> ath.com> To
> Sent by: "Charles, Roger"
> histonet-bounces@ , Kim
> Merriam
> lists.utsouthwest
>
> ern.edu cc
>
> histonet@lists.utsouthwestern.edu
>
> Subject
> 02/05/2008 02:39 Re: [Histonet] Slide printers
> (ink)
> PM
>
>
>
>
>
>
>
>
>
> Roger- We have been using a sakura slide printer for a couple of
> years. I
> do
> agree with your comments about the software - not user friendly at
> all nor
> is it intuitive. I have used Access database in the past without these
> issues. I do not know about the labels, I don't think we've had that
> issue.
> Maybe it varies with the label. I don't quite understand your
> comment on
> charged slides, as all of the slides we put thru the printer are
> charged
> and
> we have no issues with that. We use charged slides (Okando Plus)
> from BBC
> and Probe-On Plus slides from ThermoFisher. What brand of slides
> were you
> using & what issue did you have with the slide printer from the usage?
>
>
> Patti Loykasek BS, HTL, QIHC
> PhenoPath Laboratories
> Seattle, WA
>
>
>
>
>
>
>
>> Hello,
>> Recently we bought a sakura slide writer that uses ink to print. The
>> only problem I have found with the ink is if you put labels over the
>> print and then try to remove the label to verify a number error, or
>> something like that, the ink will actually come off with the
>> label. If
>> you can read upside down you can still verify the number. I did run
>> this ink thru a battery of chemicals including straight formic acid
>> for
>> 5 minutes and the ink did not leave the slide. I would caution in
>> buying a Sakura slide write as it has a very unfriendly Access based
>> program and the writer does not work with charged slides. This has
>> been
>> verified by me and an independent engineer sent to look at this
>> issue.
>> I do use a TBS cassette writer and love that so if I can get my
>> sakura
>> sent back I will be looking at TBS's slide writer too.
>> Good luck
>> Roger
>>
>> Roger Charles
>> Microbiologist
>> Pennsylvania Veterinary Laboratory
>> 2305 N Cameron St
>> Harrisburg, PA 17110
>> 717-787-8808
>>
>> -----Original Message-----
>> From: histonet-bounces@lists.utsouthwestern.edu
>> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Kim
>> Merriam
>> Sent: Tuesday, February 05, 2008 2:48 PM
>> To: Histonet
>> Subject: [Histonet] Slide printers (ink)
>>
>> Hi everyone,
>>
>> I was wondering what everyone's experience was with the TBS slide
>> printer (Shurmark-plus), the one that prints with ink? I would
>> appreciate input, good or bad.
>>
>> We currently have an etcher, and we hate it, so we are looking to
>> trade it in for something that uses ink. I have used the Leica
>> printer
>> in the past and have had reasonably good luck with it, but I was
>> wondering about the printer from TBS, I don't know anyone that has
>> one.
>>
>> Kim
>>
>>
>> Kim Merriam, MA, HT(ASCP)
>> Cambridge, MA
>>
>> ---------------------------------
>> Be a better friend, newshound, and know-it-all with Yahoo! Mobile.
>> Try
>> it now.
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>>
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>>
>
>
>
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>
>
> ------------------------------
>
> Message: 13
> Date: Tue, 5 Feb 2008 13:46:41 -0800 (PST)
> From: Rene J Buesa
> Subject: Re: [Histonet] Immunoperoxidase Double staining protocol
> To: Reuel Cornelia ,
> histonet@lists.utsouthwestern.edu
> Message-ID: <784337.61146.qm@web61225.mail.yahoo.com>
> Content-Type: text/plain; charset=iso-8859-1
>
> Generally speaking you will have to run the whole protocol for one
> of the Abs and use one chromogen (of your selection). After that,
> since you already did HIER and blocked the internal peroxidase, you
> will treat the section with the second Ab, will link/detect it and
> use another chromogen that ideally should have a different color.
> The first chromogen could be regular DAB and for the second you can
> use also DAB but with incorporated nickel that will give a deep/blue
> purple color, in contrast with the brown/reddish normal color of the
> DAB.
> The thing is that you don't need any special protocol, just your
> regular IHC protocol for FFPE tissue, run twice with two different
> chromogens.
> René J.
>
> Reuel Cornelia wrote:
> I was asked to do an immunoperoxidase double staining on
> CD61 ,Cd42, pf4 with an unknown mouse antibody that will work on
> platelets. Can somebody help me or any protocol available that I can
> refer to. I am used of IF double stianing but not Immunoperoxidase.
> Thank you.
>
> Reuel Cornelia, BS MT, AMT
> Cellular Pathology
> Texas Scottish Rite Hospital for Children
> 2222 Welborn Street
> Dallas, TX 75219
> Tel: 214-559-7766
> fax: 214-559-7768
>
> *******************************************************************************************************************
> Texas Scottish Rite Hospital for Children is one of the nation's
> leading pediatric centers for the
> treatment of orthopedic conditions, certain related neurological
> disorders and learning disorders,
> such as dyslexia. This email transmission and/or its attachments may
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> named above.
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> The authorized recipient of this information is prohibited from
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> Try it now.
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> ------------------------------
>
> Message: 14
> Date: Tue, 5 Feb 2008 15:47:03 -0600
> From: "Sebree Linda A."
> Subject: [Histonet] thanks for the support and good wishes
> To: "Histonet"
> Message-ID:
> >
>
> Content-Type: text/plain; charset="US-ASCII"
>
> Hi all,
>
> Well apparently our CAP inspector took the word of our supervisor on
> everything pertaining to our lab, reviewed some of our slides and was
> out the door before the weather associated with the "winter storm
> warning" arrived! Some times its good to live in the land of ice and
> snow!
>
> Thanks for all the good luck wishes!
>
> Linda Sebree, HT(ASCP)
> University of Wisconsin Hospital & Clinics
> IHC/ISH Laboratory
> A4/204-3224
> 600 Highland Ave.
> Madison, WI 53792
> (608)265-6596
> FAX: (608)262-7174
>
>
>
> ------------------------------
>
> Message: 15
> Date: Tue, 5 Feb 2008 16:50:57 -0600
> From: "Margaryan, Naira"
> Subject: [Histonet] (no subject)
> To:
> Message-ID:
> >
>
> Content-Type: text/plain; charset="us-ascii"
>
> Dear histo team,
>
>
>
> I need to stain frozen & FFPE sections for Tuj-1 (AbCam, ab53234) and
> FFPE sectiond for Netrin-1 (AbCam, ab39370). Any kind of suggestions
> or
> even full IHC or IF protocol is appreciated.
>
>
>
> Thanks in advance,
>
> Naira
>
>
>
>
>
>
>
>
>
> ------------------------------
>
> Message: 16
> Date: Tue, 05 Feb 2008 17:36:48 -0600
> From: Colleen Forster
> Subject: [Histonet] Do mice have tonsils??
> To: histonet@lists.utsouthwestern.edu
> Message-ID: <47A8F310.20905@umn.edu>
> Content-Type: text/plain; charset=ISO-8859-1; format=flowed
>
> For any of you have done mouse necropsy, do they have tonsils or just
> lymph nodes? I have had a request for mouse tonsils.... can't seem to
> find them in my searches. I would appreciate any help on this one.
>
> Thanks,
>
> Colleen Forster
> U of MN
>
>
>
> ------------------------------
>
> Message: 17
> Date: Tue, 5 Feb 2008 15:32:31 -0800
> From: "Breisch, Eric"
> Subject: [Histonet] eosinophils on frozen section
> To:
> Message-ID:
> <43B97B4C402C2C44AAA2A8D2C86A88B31A5A78@e2k3backend1.RCHSD.org>
> Content-Type: text/plain; charset="US-ASCII"
>
> To all interested Histonetters:
>
>
>
>
>
> We are experiencing some frustration with our ability to identify
> eosinophils from frozen sections. For some reason which our frozen
> section set up does not enable us to identify eosinophils. Eosinophil
> identification is not impaired when the tissue is submitted for
> permanents. Could some one please share the reagents used and how the
> frozen section staining area is set up if they have success
> identifying
> eosinophils from a frozen section? We have had many frozen sections
> done
> on fresh tissues suspicious for an eosinophilic granuloma but our
> techniques so far have not rendered consistent eosinophil
> identification. We presently are using 95% ETOH for fixing the FS
> slide,
> quick wash in distilled H2O, 1 minute in Richard Allen Hematoxylin 2,
> rinse in tap water, 15 seconds in bluing, rinse in water, rinse in 70%
> ETOH, 1 minute in Richard Allen Eosin Y, three rinses in 95% ETOH,
> three
> rinses in Xylene substitute and then coverslip. All other tissues
> appear
> just fine but the eosinophils just don't show up. Any suggestions are
> greatly appreciated.
>
>
>
>
>
> Eric A. Breisch, Ph.D.
>
> Clinical Anatomist
>
> Dept. of Pathology
>
> Rady Children's Hospital and Health Center
>
> Associate Clinical Professor of Anatomy
>
> Dept. of Surgery
>
> UCSD School of Medicine
>
>
>
>
>
> ------------------------------
>
> Message: 18
> Date: Tue, 5 Feb 2008 18:08:15 -0600
> From: "Ingles Claire"
> Subject: RE: [Histonet] eosinophils on frozen section
> To:
> Message-ID:
> <08A0A863637F1349BBFD83A96B27A50A1200DF@uwhis-xchng3.uwhis.hosp.wisc.edu
> >
>
> Content-Type: text/plain; charset="iso-8859-1"
>
> Eric:
> My guess is that the alcohol is lysing(blowing up) the unfixed
> eosinophils, therefore they are not there to stain. Fixation
> stabilizes the cells in order to be stained in regular paraffin
> sections. Unfortunately, I have done a few trials using different
> fixatives for fresh tissue to see if I could preserve these little
> suckers. Nothing really worked satisfactorally. You might try fixing
> in formalin for a minute or two before you continue on with your
> stain and see if this helps. (don't forget to wash the sections
> afterward) Hope this helps.
> Claire
>
>
>
> We are experiencing some frustration with our ability to identify
> eosinophils from frozen sections. For some reason which our frozen
> section set up does not enable us to identify eosinophils. Eosinophil
> identification is not impaired when the tissue is submitted for
> permanents. Could some one please share the reagents used and how the
> frozen section staining area is set up if they have success
> identifying
> eosinophils from a frozen section? We have had many frozen sections
> done
> on fresh tissues suspicious for an eosinophilic granuloma but our
> techniques so far have not rendered consistent eosinophil
> identification. We presently are using 95% ETOH for fixing the FS
> slide,
> quick wash in distilled H2O, 1 minute in Richard Allen Hematoxylin 2,
> rinse in tap water, 15 seconds in bluing, rinse in water, rinse in 70%
> ETOH, 1 minute in Richard Allen Eosin Y, three rinses in 95% ETOH,
> three
> rinses in Xylene substitute and then coverslip. All other tissues
> appear
> just fine but the eosinophils just don't show up. Any suggestions are
> greatly appreciated.
>
>
>
>
>
> Eric A. Breisch, Ph.D.
>
> Clinical Anatomist
>
> Dept. of Pathology
>
> Rady Children's Hospital and Health Center
>
> Associate Clinical Professor of Anatomy
>
> Dept. of Surgery
>
> UCSD School of Medicine
>
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
>
> ------------------------------
>
> Message: 19
> Date: Tue, 5 Feb 2008 17:30:17 -0700
> From: "Gayle Callis"
> Subject: A gentle reminder about using subject line Re: [Histonet] (no
> subject)
> To: "Margaryan, Naira" ,
>
> Message-ID: <000601c86857$72c69700$6601a8c0@Sunney>
> Content-Type: text/plain; format=flowed; charset="iso-8859-1";
> reply-type=original
>
> For those new to or not used to the Histonet messaging, please use the
> subject line rather ant just hit the reply key. Replying to the daily
> digest also kicks back all the messages for that day to those who have
> already received them. The subject is important so others, including
> me,
> don't just hit the delete key and not read your valuable inquiries and
> comment.
>
> Thanks
> Gayle M. Callis
> HTL/HT/MT(ASCP)
> Bozeman MT 59715
>
>
> ----- Original Message -----
> From: "Margaryan, Naira"
> To:
> Sent: Tuesday, February 05, 2008 3:50 PM
> Subject: [Histonet] (no subject)
>
>
> Dear histo team,
>
>
>
> I need to stain frozen & FFPE sections for Tuj-1 (AbCam, ab53234) and
> FFPE sectiond for Netrin-1 (AbCam, ab39370). Any kind of suggestions
> or
> even full IHC or IF protocol is appreciated.
>
>
>
> Thanks in advance,
>
> Naira
>
>
>
>
>
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
>
> ------------------------------
>
> Message: 20
> Date: Tue, 5 Feb 2008 19:35:12 -0500
> From: "Weems, Joyce"
> Subject: RE: [Histonet] eosinophils on frozen section
> To: "Ingles Claire" ,
>
> Message-ID:
> <1CD6831EB9B26D45B0A3EAA79F7EBD320518E56A@sjhaexc02.sjha.org>
> Content-Type: text/plain; charset="us-ascii"
>
> Fix in formal-alcohol (no, it is not wearing a tuxedo) 90 ml absolute
> alcohol - 10 ml 37% formaldehyde... Should work ok then... j
>
> -----Original Message-----
> From: histonet-bounces@lists.utsouthwestern.edu
> [mailto:histonet-bounces@lists.utsouthwestern.edu] On Behalf Of Ingles
> Claire
> Sent: Tuesday, February 05, 2008 7:08 PM
> To: histonet@lists.utsouthwestern.edu
> Subject: RE: [Histonet] eosinophils on frozen section
>
> Eric:
> My guess is that the alcohol is lysing(blowing up) the unfixed
> eosinophils, therefore they are not there to stain. Fixation
> stabilizes
> the cells in order to be stained in regular paraffin sections.
> Unfortunately, I have done a few trials using different fixatives for
> fresh tissue to see if I could preserve these little suckers. Nothing
> really worked satisfactorally. You might try fixing in formalin for a
> minute or two before you continue on with your stain and see if this
> helps. (don't forget to wash the sections afterward) Hope this helps.
> Claire
>
>
>
> We are experiencing some frustration with our ability to identify
> eosinophils from frozen sections. For some reason which our frozen
> section set up does not enable us to identify eosinophils. Eosinophil
> identification is not impaired when the tissue is submitted for
> permanents. Could some one please share the reagents used and how the
> frozen section staining area is set up if they have success
> identifying
> eosinophils from a frozen section? We have had many frozen sections
> done
> on fresh tissues suspicious for an eosinophilic granuloma but our
> techniques so far have not rendered consistent eosinophil
> identification. We presently are using 95% ETOH for fixing the FS
> slide,
> quick wash in distilled H2O, 1 minute in Richard Allen Hematoxylin 2,
> rinse in tap water, 15 seconds in bluing, rinse in water, rinse in 70%
> ETOH, 1 minute in Richard Allen Eosin Y, three rinses in 95% ETOH,
> three
> rinses in Xylene substitute and then coverslip. All other tissues
> appear
> just fine but the eosinophils just don't show up. Any suggestions are
> greatly appreciated.
>
>
>
>
>
> Eric A. Breisch, Ph.D.
>
> Clinical Anatomist
>
> Dept. of Pathology
>
> Rady Children's Hospital and Health Center
>
> Associate Clinical Professor of Anatomy
>
> Dept. of Surgery
>
> UCSD School of Medicine
>
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
> Confidentiality Notice ** The information contained in this message
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> recipient nor the employee or agent responsible for delivering this
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>
>
>
> ------------------------------
>
> Message: 21
> Date: Tue, 5 Feb 2008 17:49:57 -0700
> From: "Gayle Callis"
> Subject: Re: [Histonet] Do mice have tonsils??
> To: "Colleen Forster" ,
>
> Message-ID: <000e01c8685a$321bd7d0$6601a8c0@Sunney>
> Content-Type: text/plain; format=flowed; charset="iso-8859-1";
> reply-type=response
>
> Colleen,
>
> Rodents do NOT have tonsils, but have tissues analogous (Sp?) to
> tonsils,
> called nasal associated lymphoid tissues located in a rather
> difficult spot
> at the back of the nasal turbinates. I suggest you get into the
> literature
> and type in murine NALT as there are some excellent articles on
> morphology
> and their location. If you want to do frozen sections, you either
> need to
> remove these from this area, not easy to do, and takes a lot of
> practice OR
> you can do undecalcified bone frozen sections with the Cryojane.
> The NALT
> is located above the soft palate, just below the 3rd palatine ridge
> if you
> start counting ridges on the soft palate and starting count at the
> front
> incisors. These tiny lymphoid tissues are nestled on the roof of
> the mouth,
> just below the soft palate, between the back molars. The molars are
> the
> complicating factor for doing murine CD markers that only work on
> frozen
> sections. I will be happy to send you a powerpoint photograph of a
> fully
> decalcified mouse head, mid sagittal section, stained with H&E to show
> exactly where the NALT is located. I also have a cross section of the
> murine nasal turbinates showing NALT in that orientation, and much
> harder to
> deal with in order to find the NALT. One project had PLP perfused
> mouse
> head, immersion fixed longer and then EDTA decalcified,
> cryoprotected and
> sectioned on the cryostat to do immunoglobulin staining of turbinate
> epithelial cells back and into the NALT.
>
> We work with NALT a good deal, and I can honestly say that
> dissection/removal is not easy. However, it can be done but with very
> gentle, light touch using a pointed, tiny scalpel blade. When we do
> frozen
> sections of removed NALT, we can obtain approx 30 - 40 sections,
> serial, at
> 5 um and with treated animals to produce inflammed NALT, up to 50
> and more
> serial sections. With undecalcified bone, we get far fewer due to the
> difficulty of sectioning.
>
> G0 into PUBMED, and look for David Pascual, Keri Cscentis on their
> NALT
> publication. I believe they put a cartoon of NALT location in that
> publication.
>
> Good luck,
>
> Gayle M. Callis
> HTL/HT/MT(ASCP)
> Bozeman MT 59715
>
>
> ----- Original Message -----
> From: "Colleen Forster"
> To:
> Sent: Tuesday, February 05, 2008 4:36 PM
> Subject: [Histonet] Do mice have tonsils??
>
>
>> For any of you have done mouse necropsy, do they have tonsils or just
>> lymph nodes? I have had a request for mouse tonsils.... can't seem
>> to find
>> them in my searches. I would appreciate any help on this one.
>>
>> Thanks,
>>
>> Colleen Forster
>> U of MN
>>
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
>
> ------------------------------
>
> Message: 22
> Date: Tue, 5 Feb 2008 17:58:05 -0700
> From: "Gayle Callis"
> Subject: Re: [Histonet] eosinophils on frozen section
> To: "Breisch, Eric" ,
>
> Message-ID: <001401c8685b$55212f90$6601a8c0@Sunney>
> Content-Type: text/plain; format=flowed; charset="iso-8859-1";
> reply-type=original
>
> We improved our eosinophil staining on frozen sections of murine
> tissue by
> switching to NBF immersion fixation, let it sit 10 min, then do the
> H&E but
> use eosin/phloxine (Richard Allan stain will work) but stain in
> eosin/phloxine for 2 minutes. For some reason, the eosin was
> never taken
> up as well after a shorter time in eosin alone, and greatly
> improved with
> the phloxine added. Sections can be cut a bit thinner too, try 4 um
> - it
> should make the granules more apparent against the background and
> other
> cells. Also, I suggest adding absolute alcohol after the 95% for
> better
> dehydration before clearing.
>
> You may have success using alcoholic formalin in order to speed up the
> fixation a bit. However, when we switched to NBF, we had better
> staining of
> eosinophils in frozen sections. If you have the time, you can let NBF
> fixation go longer, we often let sections sit for days then stain,
> but with
> your diagnostic procedure, you will want a bit more speed involved.
>
> Good luck
>
> Gayle M..Callis
> HTL/HT/MT(ASCP)
> Bozeman MT 59715
>
>
>
>
>
>
> ----- Original Message -----
> From: "Breisch, Eric"
> To:
> Sent: Tuesday, February 05, 2008 4:32 PM
> Subject: [Histonet] eosinophils on frozen section
>
>
> To all interested Histonetters:
>
>
>
>
>
> We are experiencing some frustration with our ability to identify
> eosinophils from frozen sections. For some reason which our frozen
> section set up does not enable us to identify eosinophils. Eosinophil
> identification is not impaired when the tissue is submitted for
> permanents. Could some one please share the reagents used and how the
> frozen section staining area is set up if they have success
> identifying
> eosinophils from a frozen section? We have had many frozen sections
> done
> on fresh tissues suspicious for an eosinophilic granuloma but our
> techniques so far have not rendered consistent eosinophil
> identification. We presently are using 95% ETOH for fixing the FS
> slide,
> quick wash in distilled H2O, 1 minute in Richard Allen Hematoxylin 2,
> rinse in tap water, 15 seconds in bluing, rinse in water, rinse in 70%
> ETOH, 1 minute in Richard Allen Eosin Y, three rinses in 95% ETOH,
> three
> rinses in Xylene substitute and then coverslip. All other tissues
> appear
> just fine but the eosinophils just don't show up. Any suggestions are
> greatly appreciated.
>
>
>
>
>
> Eric A. Breisch, Ph.D.
>
> Clinical Anatomist
>
> Dept. of Pathology
>
> Rady Children's Hospital and Health Center
>
> Associate Clinical Professor of Anatomy
>
> Dept. of Surgery
>
> UCSD School of Medicine
>
>
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
>
>
>
> ------------------------------
>
> Message: 23
> Date: Tue, 5 Feb 2008 20:06:55 -0600
> From: Julia Dahl
> Subject: RE: [Histonet] eosinophils on frozen section
> To: "Breisch, Eric" ,
>
> Message-ID:
> Content-Type: text/plain; charset="iso-8859-1"
>
>
> Agree with Gayle that alcoholic formalin allows for speedier
> fixation and preservation of eosinophil granule membranes (and
> therefore staining, rather than degranulation).
>
>> Date: Tue, 5 Feb 2008 15:32:31 -0800
>> From: ebreisch@rchsd.org
>> To: histonet@lists.utsouthwestern.edu
>> Subject: [Histonet] eosinophils on frozen section
>>
>> To all interested Histonetters:
>>
>>
>>
>>
>>
>> We are experiencing some frustration with our ability to identify
>> eosinophils from frozen sections. For some reason which our frozen
>> section set up does not enable us to identify eosinophils. Eosinophil
>> identification is not impaired when the tissue is submitted for
>> permanents. Could some one please share the reagents used and how the
>> frozen section staining area is set up if they have success
>> identifying
>> eosinophils from a frozen section? We have had many frozen sections
>> done
>> on fresh tissues suspicious for an eosinophilic granuloma but our
>> techniques so far have not rendered consistent eosinophil
>> identification. We presently are using 95% ETOH for fixing the FS
>> slide,
>> quick wash in distilled H2O, 1 minute in Richard Allen Hematoxylin 2,
>> rinse in tap water, 15 seconds in bluing, rinse in water, rinse in
>> 70%
>> ETOH, 1 minute in Richard Allen Eosin Y, three rinses in 95% ETOH,
>> three
>> rinses in Xylene substitute and then coverslip. All other tissues
>> appear
>> just fine but the eosinophils just don't show up. Any suggestions are
>> greatly appreciated.
>>
>>
>>
>>
>>
>> Eric A. Breisch, Ph.D.
>>
>> Clinical Anatomist
>>
>> Dept. of Pathology
>>
>> Rady Children's Hospital and Health Center
>>
>> Associate Clinical Professor of Anatomy
>>
>> Dept. of Surgery
>>
>> UCSD School of Medicine
>>
>>
>>
>> _______________________________________________
>> Histonet mailing list
>> Histonet@lists.utsouthwestern.edu
>> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
> _________________________________________________________________
> Connect and share in new ways with Windows Live.
> http://www.windowslive.com/share.html?ocid=TXT_TAGHM_Wave2_sharelife_012008
>
> ------------------------------
>
> _______________________________________________
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet
>
> End of Histonet Digest, Vol 51, Issue 7
> ***************************************
Laura R Hunt, PhD
Post-doctoral associate
University of Texas at Arlington
ph: 817-272-1499
fax: 817-272-2855
lhunt@uta.edu
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