RE: Daily Digest

From:Felisha Sandifer

When I asked about histology at home I did not mean a full histology lab
with all types of flamable liquids and carcinogens (laughing). What I have
heard is that people simply cut blocks at home which would just consist of
a microtome and waterbath and an oven to bake the slides. I guess I should
clarify before more panic sets in.

--- Felisha Sandifer
--- leish27@earthlink.net
--- EarthLink: The #1 provider of the Real Internet.


> [Original Message]
> From: HistoNet Server 
> To: HistoNet Server 
> Date: 10/8/2002 12:59:38 AM
> Subject: Daily Digest
>
>
> ----------------------------------------------------------------------
>
> Date: 7 Oct 2002 02:31:01 -0500
> From: louise renton 
> Subject: Re: Soap
>
> Would heat and solvents of normal processing not alter the structure?
What 
> about frozen sections?
>
> >From: marjorie lehman 
> >To: histonet 
> >Subject: Soap
> >Date: Fri, 04 Oct 2002 12:06:06 -0400
> >
> >Hi,
> >Does anyone have any suggestions/methods/thoughts on sectioning a piece
of
> >soap? Actually, it is not a true soap, it's a detergent bar/"Beauty Bar"
> >(whatever) and the investigator is looking for structure after the bar
has 
> >been
> >extruded (formed into a cake).  Oh my, I do get asked to cut strange 
> >things!!
> >Thanks,
> >Marge Lehman
>
>
>
>
> Louise Renton
> Bone Research Unit
> MRC
> Johannesburg
> South Africa
> Tel & fax +27 11 717 2298
> "Time flies like an arrow, fruit flies like a banana"
>
>
> _________________________________________________________________
> Join the worldis largest e-mail service with MSN Hotmail. 
> http://www.hotmail.com
>
>
>
> ----------------------------------------------------------------------
>
> Date: 7 Oct 2002 07:15:47 -0500
> From: "Morken, Tim" 
> Subject: New or imporved  RE: National COnference
>
>
> Cheryl wrote: < for those of us who couldn't make it?>>
>
> I learned that Rockbottoms in Long Beach has a very good Octoberfest
lager.
> And the smoked-chicken enchiladas were good as well. 
>  
>  
> Tim
> Atlanta
>
> - -----Original Message-----
> From: Cheryl Powell [mailto:cherylhisto@hotmail.com]
> Sent: Sunday, October 06, 2002 5:06 PM
> To: histonet@pathology.swmed.edu
> Subject: National COnference
>
>
> Hi everybody!  So how was the NSH national meetings?  COUld people share
> something they learned new or improved for those of us who couldn't make
it?
>
>
>
> Cheryl Ann Powell B.S., HTL(ASCP) 
> Botsford General Hospital 
> Farmington Hills, MI USA 
>
>   _____  
>
> Chat with friends online, try MSN Messenger: Click
>  Here
>
>
>
>
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> 
class=855494911-07102002> face="Times New Roman" color=#000000 size=3>Cheryl wrote: <<Could people > > share something they learned new or improved for those of us who couldn't make > > it?>>
>
I > learned that Rockbottoms in Long Beach has a very good Octoberfest lager. And > the smoked-chicken enchiladas were good as well.
>
class=855494911-07102002> 
>
class=855494911-07102002> 
>
class=855494911-07102002>Tim
>
class=855494911-07102002>Atlanta
>
>
size=2>-----Original Message-----
From: Cheryl Powell > [mailto:cherylhisto@hotmail.com]
Sent: Sunday, October 06, 2002 > 5:06 > PM
To: histonet@pathology.swmed.edu
Subject: National > COnference

>
>
>
Hi everybody!  So how was the NSH national meetings?  > COUld people share something they learned new or improved for those of us > who > couldn't make it?


>
Cheryl Ann Powell B.S., > HTL(ASCP)
Botsford > General Hospital >
>
Farmington Hills, MI > USA >

>
> Chat with friends online, try MSN Messenger: href="http://g.msn.com/1HM1ENUS/c144??PS=47575">Click > Here
> > - --Boundary_(ID_BxzfiSuYpVGrhuPAZlK1gg)-- > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 07:30:15 -0500 > From: rkline@emscience.com > Subject: Re: Buffer recipe > > > Marina, > I'm not sure Soerensen's buffer is the proper buffer to Giemsa. The salt > combinations in buffers can effect staining. Have you tried the Gurr > tablets from Merck? > Rande Kline > EM Science > > > > > marina goumenou on 10/05/2002 04:25:47 PM > > To: histonet@pathology.swmed.edu > cc: > Subject: Buffer recipe > > > > Hello to everybody! > > Your suggestions for my May Grunwald - Giemsa problems were really very > helpfull. However, I stained my slides with dye solutions in Soerensen > buffer pH 6,8 but they appeared to be too blue. So I intent to use even > lower pH value (something like 6,0 or 6,2). Does anybody have a recipe for > apropriate buffer (Soerensen or anything you think) in these pH values? > Thanking you in advance > Best Regards > Marina Goumenou > Athens - Greece > > > _________________________________________________________________ > Join the worldis largest e-mail service with MSN Hotmail. > http://www.hotmail.com > > > > > > > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 08:30:09 -0500 > From: "Johnston, Kathy" > Subject: RE: Buffer recipe > > This is my table: > > You have your 2 stock buffer solutions: > 1. M/15 sodium phosphate dibasic (Na2HPO4) - dissolve 9.465 g in 1L dH2O. > 2. M/15 potassium acid phosphate (KH2PO4) - dissolve 9.08 g in 1L dH2O. > > To make the amounts of each solution follow the below table: > > pH M/15 KH2PO4 M/15 Na2HPO4 > mL mL > 8.0 4 96 > 7.6 12 88 > 7.2 27 73 > 6.8 50 50 > 6.4 71 29 > 6.0 88 12 > 5.6 95 5 > > Hope this helps! > > Kathy Johnston > Tech II - Special Stains > Anatomic Pathology - Foothills Medical Center > Calgary Laboratory Services > Ph - 403-944-4760 > Fax - 403-270-4093 > kathy.johnston@cls.ab.ca > > - -----Original Message----- > From: marina goumenou [mailto:mtg67@hotmail.com] > Sent: Saturday, October 05, 2002 2:26 PM > To: histonet@pathology.swmed.edu > Subject: Buffer recipe > > > > Hello to everybody! > > Your suggestions for my May Grunwald - Giemsa problems were really very > helpfull. However, I stained my slides with dye solutions in Soerensen > buffer pH 6,8 but they appeared to be too blue. So I intent to use even > lower pH value (something like 6,0 or 6,2). Does anybody have a recipe for > apropriate buffer (Soerensen or anything you think) in these pH values? > Thanking you in advance > Best Regards > Marina Goumenou > Athens - Greece > > > _________________________________________________________________ > Join the worldis largest e-mail service with MSN Hotmail. > http://www.hotmail.com > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 08:30:29 -0500 > From: "Johnston, Kathy" > Subject: RE: High Iron Diamine stain for sulphomucins > > This is what I have found, although I believe the chemicals to be quite > toxic to use. > > http://www.bris.ac.uk/pathandmicro/cpl/hidab.html > > Enjoy! > > Kathy Johnston > Tech II - Special Stains > Anatomic Pathology - Foothills Medical Center > Calgary Laboratory Services > Ph - 403-944-4760 > Fax - 403-270-4093 > kathy.johnston@cls.ab.ca > > > - -----Original Message----- > From: Martin, Ronald [mailto:Ronald.Martin@umassmed.edu] > Sent: Friday, October 04, 2002 12:14 PM > To: histonet@pathology.swmed.edu > Subject: High Iron Diamine stain for sulphomucins > > > Fellow techs, > Does anyone have a procedure they are willing to share for a High Iron > Diamine stain for sulphomucins? This is new to me so I will new information > regarding times, concentrations, chemicals etc. We are trying to > differentiate between sulfated and carboxylated components in mouse > stomach/intestine. > Thanks in advance, > Ron Martin > Research Associate > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 10:00:26 -0500 > From: "Weems, Joyce" > Subject: HistoQIP Program > > Has anyone seen what is required for this program? I believe it would be > more better than the Immuno program, but would like to hear from you before > I order! Thanks, j > > > Joyce Weems > Pathology Manager > Saint Joseph's Hospital of Atlanta > 404-851-7376 > 404-851-7831 - fax > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 10:30:17 -0500 > From: "ander093@tc.umn.edu" > Subject: Re: HistoQIP Program > > Hi all, > I am interested in this program as well. If anyone has any info.....would you > please reply to the list. Thank you. > > LuAnn Anderson > > > > > Has anyone seen what is required for this program? I believe it would be > > more better than the Immuno program, but would like to hear from you before > > I order! Thanks, j > > > > > > Joyce Weems > > Pathology Manager > > Saint Joseph's Hospital of Atlanta > > 404-851-7376 > > 404-851-7831 - fax > > > > > > > > . > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 10:46:03 -0500 > From: "Weems, Joyce" > Subject: RE: HistoQIP Program > > Oops, for anyone checking grammar I was testing you! :>) > > > Joyce Weems > Pathology Manager > Saint Joseph's Hospital of Atlanta > 404-851-7376 > 404-851-7831 - fax > > -----Original Message----- > From: Weems, Joyce > Sent: Monday, October 07, 2002 10:51 AM > To: 'Histonet' > Subject: HistoQIP Program > > Has anyone seen what is required for this program? I believe it would be > more better than the Immuno program, but would like to hear from you before > I order! Thanks, j > > > Joyce Weems > Pathology Manager > Saint Joseph's Hospital of Atlanta > 404-851-7376 > 404-851-7831 - fax > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 11:15:10 -0500 > From: Christian Wuthrich > Subject: Re: Alcian Blue staining problem > > Hi Manisha, > > Try to rinse your slides with buffer (at the same pH than your > staining solution). If possible, you also should mount your slides > with a buffered mounting medium or a quick drying medium (so that it > will not modify your stain)... > > These are the experience I get when I was studying European beech > bark (phloem, cambium) and wood sample mounted in JB-4 resin... > > Hope it helps > - -- > Christian Wuethrich > Division of viral pathogenesis > Beth Israel deaconess Medical Center > 330 Brookline Avenue > Boston, MA 02215 > United states > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 12:00:20 -0500 > From: pruegg@colobio.com > Subject: Re: New or imporved RE: National COnference > > I learned that it is bad luck to watch a Bronco monday night football > game from the Rock Bottom brewery in Long Beach, seriously though, when > I get a chance > I will put together a synopsis of some important things I learned at the > NSH S/C 2002. > Patsy Ruegg > > "Morken, Tim" wrote: > > > Cheryl wrote: < > improved for those of us who couldn't make it?>> > > I learned that Rockbottoms in Long Beach has a very good Octoberfest > > lager. And the smoked-chicken enchiladas were good as well. TimAtlanta > > > > -----Original Message----- > > From: Cheryl Powell [mailto:cherylhisto@hotmail.com] > > Sent: Sunday, October 06, 2002 5:06 PM > > To: histonet@pathology.swmed.edu > > Subject: National COnference > > > > Hi everybody! So how was the NSH national meetings? COUld > > people share something they learned new or improved for > > those of us who couldn't make it? > > > > Cheryl Ann Powell B.S., HTL(ASCP)Botsford General Hospital > > Farmington Hills, MI USA > > > > > > ------------------------------------------------------------- > > Chat with friends online, try MSN Messenger: Click Here > > > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 12:00:36 -0500 > From: pruegg@colobio.com > Subject: Re: HistoQIP Program > > Joyce, > what immuno program are you refering to? > we will be accepting the first 300 participents for HistoQip in the beginning > and there is a committee designing the program, i think the first survey will > be for H&E and trichrome with some goal for expanding into IHC down the road. > Freida Carson may be able to enlighten us further on the program content so > that we can decide to participate or not. freidac@aol.com > Patsy > "Weems, Joyce" wrote: > > > Has anyone seen what is required for this program? I believe it would be > > more better than the Immuno program, but would like to hear from you before > > I order! Thanks, j > > > > Joyce Weems > > Pathology Manager > > Saint Joseph's Hospital of Atlanta > > 404-851-7376 > > 404-851-7831 - fax > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 12:00:51 -0500 > From: "Weems, Joyce" > Subject: RE: HistoQIP Program > > CAP has a program that we have participated in for a few years. The problem > is that 1. it is geared for pathologists and 2. we often do not have all the > antibodies designated for testing. > Joyce > > > Joyce Weems > Pathology Manager > Saint Joseph's Hospital of Atlanta > 404-851-7376 > 404-851-7831 - fax > > -----Original Message----- > From: Patsy Ruegg [mailto:pruegg@colobio.com] > Sent: Monday, October 07, 2002 12:48 PM > To: Weems, Joyce; freidac@aol.com > Cc: 'Histonet' > Subject: Re: HistoQIP Program > > Joyce, > what immuno program are you refering to? > we will be accepting the first 300 participents for HistoQip in the > beginning > and there is a committee designing the program, i think the first survey > will > be for H&E and trichrome with some goal for expanding into IHC down the > road. > Freida Carson may be able to enlighten us further on the program content so > that we can decide to participate or not. freidac@aol.com > Patsy > "Weems, Joyce" wrote: > > > Has anyone seen what is required for this program? I believe it would be > > more better than the Immuno program, but would like to hear from you > before > > I order! Thanks, j > > > > Joyce Weems > > Pathology Manager > > Saint Joseph's Hospital of Atlanta > > 404-851-7376 > > 404-851-7831 - fax > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 13:30:25 -0500 > From: Melissa Jans > Subject: HT/HTL tissue list > > > > Does anyone know when the list of tissues will be mailed out for the HT/HTL > exam applications that were due on October 1st. We have some anxious people > in the lab who want to get started! > > Thanks, > > Melissa Jans > > > > > > - --------------------------------- > Do you Yahoo!? > Faith Hill - Exclusive Performances, Videos, & more > faith.yahoo.com > > > > ******************* NOTE ******************* > There may be important message content > contained in the following MIME Information. > ******************************************** > > > - ------------------ MIME Information follows ------------------ > > > - --Boundary_(ID_3c0lmgWhWMKiFbtvskvHbw) > Content-type: text/plain; charset=us-ascii > Content-transfer-encoding: 7BIT > > <<<<<< See above "Message Body" >>>>>> > > - --Boundary_(ID_3c0lmgWhWMKiFbtvskvHbw) > Content-type: text/html; charset=us-ascii > Content-transfer-encoding: 7BIT > >

Does anyone know when the list of tissues will be mailed out for the HT/HTL > exam applications that were due on October 1st.  We have some > anxious people in the lab who want to get started!

>

Thanks,

>

Melissa Jans

>

 



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> faith.yahoo.com > > - --Boundary_(ID_3c0lmgWhWMKiFbtvskvHbw)-- > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 14:00:48 -0500 > From: CYNTHIA HAYNES > Subject: lens of rat/mice > > > > Dear Histonetters, > > I would like to know if there is anyone out in H&E land who has > experience with cutting frozen sections on rat and/or mice lens. I've tried > cutting them fresh and fixed and both have left with shattered lens. Please > e-mail me with any information on how to section them correctly. > Sincerely yours, > Cynthia Haynes > > > P.S. My e-mail address is cynthiahaynes@hotmail.com > > _________________________________________________________________ > Join the worldis largest e-mail service with MSN Hotmail. > http://www.hotmail.com > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 14:16:11 -0500 > From: FreidaC@aol.com > Subject: Re: HistoQIP Program > > The new HistoQIP program is an external quality assessment program that is a > cooperative effort of the NSH and CAP. It is designed specifically for the > histotechnology laboratory. There will be two submissions a year, and each > will consists of specific H&E's and two special stains. The first submission > includes a trichrome and mucin stain, and the second will include a fungus > and an acid fast stain. You will be asked to submit a control (for special > stains) stained with the method used in your laboratory. Also information > will be collected from each laboratory on specimen preparation, reagents > used, etc. A report will go back to the laboratory with a score on each > slide, along with ratings of all other participating laboratories (not by > name of course), and along with statistics on all demographic information. > One of the most important pieces of information to be returned will be > educational material on each procedure (principle, what the pathologists is > looking for when he orders the stain, pitfalls, etc.) along with a > photograph of a good stain. We also hope to send methods from the best > performing laboratories, so that if needed, a participating laboratory can > use this to modifiy and improve their procedure. It is anticipated that some > time in the future, one of the special stains requested will be an > immunohistochemical stain. > > This program will be limited to 300 participants the first year, and then > will be opened to a larger number the second year. > > NSH is excited about the program, having worked on initiating an EQA program > for several years, and now having CAP as a co-sponsor. It is the first > program designed specifically for the anatomic pathology laboratory, and > should be a help when inspection time comes around. Those participating in > the pilot program found that the inspectors were pleased with the quality > assessment documentation provided at that time, and this will be much more > extensive. > > Hope this helps. > > Freida Carson > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 15:00:41 -0500 > From: leish27@earthlink.net > Subject: RE: Daily Digest > > Hello everyone. I was talking to some people at work and they told me some > people still do histology at home. This sounds interesting to do on a > part-time basis or something. Is this something that is gaining popularity? > Can anyone share any information on how this would be done or if they know > someone that does it I can talk to. Thanks...just curious. > > - --- Felisha Sandifer > - --- leish27@earthlink.net > - --- EarthLink: The #1 provider of the Real Internet. > > > > [Original Message] > > From: HistoNet Server > > To: HistoNet Server > > Date: 10/7/2002 1:00:10 AM > > Subject: Daily Digest > > > > > > ---------------------------------------------------------------------- > > > > Date: 6 Oct 2002 00:45:26 -0500 > > From: "Ms. Evelyn Kaplan" > > Subject: Re: Soap > > > > Hi Marjorie, > > > > Taking it that this is not a set up............. > > When I was a very raw junior, one of our laboratory jokes was to embed a > > piece of soap in wax and give it to the newest recruit of the department > to > > try and cut a section. I was the next on the hit list and of course when I > > cut a lovely 3 microns section was very disappointed when it hit the > water > > bath and disappeared. However, I floated it out on alcohol and my senior > > member of staff was amazed I had got any thing of the block! Let alone a > > section you could see. > > I am in the same position were the College of Engineering have asked me > to > > cut thin sections of black polythene waste pipes! > > Give it a try.............. > > > > Evelyn Kaplan > > Dept of Pathology, > > Sultan Qaboos University, > > Muscat, Oman > > > > > > > > ---------------------------------------------------------------------- > > > > Date: 6 Oct 2002 16:15:14 -0500 > > From: Cheryl Powell > > Subject: National COnference > > > >
> >
Hi everybody!  So how was the NSH national meetings?  > > COUld people share something they learned new or improved for those of us > who > > couldn't make it?


> >
Cheryl Ann Powell B.S., > > HTL(ASCP)
Botsford > > General Hospital > >
> >
Farmington Hills, MI > > USA > >


Chat with friends online, try MSN > > Messenger: Click > > Here
> > > > > > ---------------------------------------------------------------------- > > > > Date: 6 Oct 2002 20:45:47 -0500 > > From: Michael & Victoria Franklin > > Subject: HTL Exam > > > > Hello~ > > > > I am studying to take the HTL exam and I was hoping for some input from > > others who have taken it. > > > > If anyone could offer helpful info (subjects to pay particular attention > > to, good texts and/or study guides, etc.), I would love to hear from > > you! > > > > Many thanks, > > Vicki > > > > > > > > Here are the messages received yesterday! > > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 15:30:42 -0500 > From: Ryan Blair Rountree > Subject: Calcein Blue and Tetracycline Bone Fluorescence > > I am trying to characterize the bone deposition rates in mouse feet. I > have read several papers and plan to inject calcein blue first, wait 7 > days, inject tetracycline, wait 2 days, then plastic embed and section. > However, I still have a few questions and any tips would be greatly > appreciated. > > What dosage is best for calcein blue? I have seen it used at 32mg/kg, but > this was for sacrificing the animals 6 hours later. I plan to sacrifice > the animal 9 days later - should I use a lower dose? > > What concentration and in what (water?) do you make up the calcein blue > and tet STOCK solutions? How do you store them? > > How careful do you have to be during the sectioning to prevent light > exposure? Do you have to put the slides immediately into a dark box as > you cut, or can you wait until the session is done? > > Will a filter usually used for detecting the DNA stain DAPI that lets > 360-380nm light through excite tetracycline enough to visualize it? It's > excitation peak is 390nm (range 380-420), and this borderline. > > Thanks for your help! > > Ryan > > Ryan Rountree > Department of Developmental Biology > Stanford, CA 94305 > Fax: (650) 725-7739 > > > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 15:30:57 -0500 > From: Pamela.Neill@AlconLabs.com > Subject: Meeting of the Texas Society for Microscopy Oct. 24-26 > > The Fall 2002 TSM meeting will be held at Embassy Suites Austin North in > Austin, Texas October 24-26. Workshops , cryo-microtomy with TEM sample > preparation and TEM materials preparation tools, will be held during the > meeting. There will be podium and poster sessions Friday and Saturday. > Check out the website www.texasmicroscopy.org for more details. > > Pamela Neill > TSM President 2002-2003 > www.texasmicroscopy.org > 817-568-6497 > > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 15:45:10 -0500 > From: Cynthia Favara > Subject: RE: lens of rat/mice > > Cynthia, > > I have done mouse eye including the lens in paraffin and frozen with good > results. What information would you like to have. > > Cynthia Favara > NIAID/NIH/RML/LPVD > 903 South 4th Street > Hamilton, MT 59840 > 406-363-9317 > > > - -----Original Message----- > From: CYNTHIA HAYNES [mailto:cynthiahaynes@hotmail.com] > Sent: Monday, October 07, 2002 12:44 PM > To: histonet@pathology.swmed.edu > Subject: lens of rat/mice > > > > > Dear Histonetters, > > I would like to know if there is anyone out in H&E land who has > experience with cutting frozen sections on rat and/or mice lens. I've tried > cutting them fresh and fixed and both have left with shattered lens. Please > e-mail me with any information on how to section them correctly. > Sincerely yours, > Cynthia Haynes > > > P.S. My e-mail address is cynthiahaynes@hotmail.com > > _________________________________________________________________ > Join the worldis largest e-mail service with MSN Hotmail. > http://www.hotmail.com > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 16:15:12 -0500 > From: Instrumedics > Subject: NSH meeting > > Dear Histonetters, > We want to thank all of you who visited our booth for a demonstration of the > CryoJane Tape-Transfer technology. > > Please let us know if you need any further information. We can send you a > video that is narrated by Dr. Richard Zarbo, of the Henry Ford Hospital, > that has a full demonstration of the CryoJane process, from snap freezing > the tissue to fixation. > > This offer is open to all! > > Thanks again. > > Bernice > schiller@instrumedics.com > > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 17:16:06 -0500 > From: Robert Brunner > Subject: RE: HT/HTL tissue list > > > Melissa > > The tissue lists will probably be out around the 21st of October. > > Robert Brunner > Program Director > Argosy University > Histology Technician Program > > - -----Original Message----- > From: Melissa Jans [mailto:histomjans@yahoo.com] > Sent: Monday, October 07, 2002 1:14 PM > To: histonet@pathology.swmed.edu > Subject: HT/HTL tissue list > > > > Does anyone know when the list of tissues will be mailed out for the HT/HTL > exam applications that were due on October 1st. We have some anxious people > in the lab who want to get started! > > Thanks, > > Melissa Jans > > > > > > > _____ > > Do you Yahoo!? > Faith Hill - Exclusive Performances, Videos, & more > faith.yahoo.com > > > > > ******************* NOTE ******************* > There may be important message content > contained in the following MIME Information. > ******************************************** > > > - ------------------ MIME Information follows ------------------ > > This is a multi-part message in MIME format. > > - --Boundary_(ID_+JwSB8hh/rFsuFofgC0WcA) > Content-type: text/plain; charset=iso-8859-1 > Content-transfer-encoding: 7BIT > > <<<<<< See above "Message Body" >>>>>> > > - --Boundary_(ID_+JwSB8hh/rFsuFofgC0WcA) > Content-type: text/html; charset=iso-8859-1 > Content-transfer-encoding: 7BIT > > > > > > > > >
size=2>Melissa
>
size=2>  >
>
The > tissue lists will probably be out around the 21st of October.  >
>
size=2> 
>
size=2>Robert > Brunner
>
size=2>Program Director
>
size=2>Argosy > University
>
size=2>Histology Technician Program
>
>
size=2>-----Original Message-----
From: Melissa Jans > [mailto:histomjans@yahoo.com]
Sent: Monday, October 07, 2002 1:14 > PM
To: histonet@pathology.swmed.edu
Subject: HT/HTL > tissue > list

>

Does anyone know when the list of tissues will be mailed out for the > HT/HTL > exam applications that were due on October 1st.  We have some > anxious people in the lab who want to get started!

>

Thanks,

>

Melissa Jans

>

 

>


>


> Do you Yahoo!?
Faith Hill - > Exclusive > Performances, Videos, & more
href="http://faith.yahoo.com">faith.yahoo.com >
> > - --Boundary_(ID_+JwSB8hh/rFsuFofgC0WcA)-- > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 19:30:24 -0500 > From: Lee & Peggy Wenk > Subject: Re: HT/HTL tissue list > > > For those who would like to start collecting the registry practical tissues > early - go to the following web site of ASCP Board of Registry: > > http://www.ascp.org/bor/certification/procedures > > Then either click on Histologic Technician or Histotechnologists, depending if > you are planning on taking the HT or HTL exam. This will get you to a page > (for each) that lists the routes. Scroll to the bottom of the routes page. At > the bottom, is a link to the practical exam (for each). > > On the practical exam list is ALL the possible tissues they might ask you to > collect, and ALL the possible stains on each tissues, that they might ask for. > For the HTL, that's 28 tissues, with between 1 and 6 stains for each tissue. > For the HT, that's 25 tissues, with between 1 and 5 stains for each tissue. > > So the 9 tissues/stains the BOR will ask for each practical will come off > these lists - HT and HTL. > > For my students, we start collecting tissues months BEFORE they ever receive > their exam lists. We use these web site lists to collect the tissues, get the > correct components, gross them the right dimensions, etc. We process the > tissue, embed them, and cut and stain and do an H&E. We then look at the H&E. > If the tissue/block is good, we hang onto it, just in case the BOR asks for > that tissue. If the tissue isn't good enough (too small, slightly autolyzed, > wrong part of the organ, etc), we know to go looking for better. > > By collecting early off of this list, then once the "official" exam list > comes, we already have a good head start on the collection of tissues. And > sometimes, finding a colon or gallbladder with columnar epithelium across one > entire surface can be surprisingly difficult. Or finding an ovary or tonsil > that's 1.5 x 1.5 cm square can also be difficult, as it needs to be this size > so that it can shrink in processing yet remains bigger than the 1.0 x 1.0 cm > square requirement. > > Each year, we have one tissue that gives us problems. Stomach one year, > esophagus another, gall bladder another. It was liver last year. And each > year, it's a different tissue that seems to give us difficulties. We will just > have problem getting a good, non-autolyzed, well fixed, epithelium all intact, > tissue on one tissue. And that's with starting months in advance. > > So my advise is . . . collect early, collect often, collect a lot. > > Hope that helps. > > Peggy A. Wenk, HTL(ASCP)SLS > William Beaumont Hospital > Royal Oak, MI 48073 > > > ----- Original Message ----- > From: Melissa Jans > To: histonet@pathology.swmed.edu > Sent: Monday, October 07, 2002 2:13 PM > Subject: HT/HTL tissue list > > > Does anyone know when the list of tissues will be mailed out for the HT/HTL > exam applications that were due on October 1st. We have some anxious people > in the lab who want to get started! > > Thanks, > > Melissa Jans > > > > > > > > - > ---------------------------------------------------------------------------- -- > Do you Yahoo!? > Faith Hill - Exclusive Performances, Videos, & more > faith.yahoo.com > > > > ******************* NOTE ******************* > There may be important message content > contained in the following MIME Information. > ******************************************** > > > - ------------------ MIME Information follows ------------------ > > This is a multi-part message in MIME format. > > - --Boundary_(ID_Y9tPqDCSVjm07OMIe5Qp/Q) > Content-type: text/plain; charset=iso-8859-1 > Content-transfer-encoding: 7BIT > > <<<<<< See above "Message Body" >>>>>> > > - --Boundary_(ID_Y9tPqDCSVjm07OMIe5Qp/Q) > Content-type: text/html; charset=iso-8859-1 > Content-transfer-encoding: 7BIT > > > > > > > > >
For those who would like to start collecting the > registry practical tissues early - go to the following web site of ASCP Board > of > Registry:
>
 
> >
 
>
Then either click on Histologic Technician or > Histotechnologists, depending if you are planning on taking the HT or HTL > exam. > This will get you to a page (for each) that lists the routes. Scroll to the > bottom of the routes page. At the bottom, is a link to the practical exam (for > > each).
>
 
>
On the practical exam list is ALL the possible > tissues they might ask you to collect, and ALL the possible stains on each > tissues, that they might ask for. For the HTL, that's 28 tissues, with between > 1 > and 6 stains for each tissue. For the HT, that's 25 tissues, with between 1 > and > 5 stains for each tissue.
>
 
>
So the 9 tissues/stains the BOR will ask for each > > practical will come off these lists - HT and HTL.
>
 
>
For my students, we start collecting tissues > months > BEFORE they ever receive their exam lists. We use these web site lists to > > collect the tissues, get the correct components, gross them the right > dimensions, etc. We process the tissue, embed them, and cut and stain and do > an > H&E. We then look at the H&E. If the tissue/block is good, we hang > onto > it, just in case the BOR asks for that tissue. If the tissue isn't good enough > > (too small, slightly autolyzed, wrong part of the organ, etc), we know to go > looking for better.
>
 
>
By collecting early off of this list, then once > the > "official" exam list comes, we already have a good head start on the > collection > of tissues. And sometimes, finding a colon or gallbladder with columnar > epithelium across one entire surface can be surprisingly difficult. Or finding > > an ovary or tonsil that's 1.5 x 1.5 cm square can also be difficult, as it > needs > to be this size so that it can shrink in processing yet remains bigger > than > the 1.0 x 1.0 cm square requirement.
>
 
>
Each year, we have one tissue that gives us > problems. Stomach one year, esophagus another, gall bladder another. It was > liver last year. And each year, it's a different tissue that seems to give us > difficulties. We will just have problem getting a good, non-autolyzed, > well > fixed, epithelium all intact, tissue on one tissue. And that's with starting > months in advance.
>
 
>
So my advise is . . . collect early, collect > > often, collect a lot.
>
 
>
Hope that helps.
>
 
>
Peggy A. Wenk, HTL(ASCP)SLS
>
William Beaumont Hospital
>
Royal Oak, MI 48073
>
 
>
 
>
style="PADDING-RIGHT: 0px; PADDING-LEFT: 5px; MARGIN-LEFT: 5px; BORDER-LEFT: > #000000 2px solid; MARGIN-RIGHT: 0px"> >
----- Original Message -----
>
style="BACKGROUND: #e4e4e4; FONT: 10pt arial; font-color: > black">From: > Melissa > Jans
> >
Sent: Monday, October 07, 2002 2:13 > PM
>
Subject: HT/HTL tissue list
>

>

Does anyone know when the list of tissues will be mailed out for the > HT/HTL > exam applications that were due on October 1st.  We have some > anxious people in the lab who want to get started!

>

Thanks,

>

Melissa Jans

>

 

>


>


> Do you Yahoo!?
Faith Hill - > Exclusive > Performances, Videos, & more
href="http://faith.yahoo.com">faith.yahoo.com >
> > - --Boundary_(ID_Y9tPqDCSVjm07OMIe5Qp/Q)-- > > > ---------------------------------------------------------------------- > > Date: 7 Oct 2002 19:30:39 -0500 > From: Melissa Jensen > Subject: Re: written portion of HT > > CONGRATS!!!!!!!! WELL DONE! > - ----- Original Message ----- > From: > To: > Sent: Saturday, October 05, 2002 1:22 PM > Subject: Re: written portion of HT > > > > I was the one last week that thought I bombed the written portion of the > HT. I passed!!!!! Just had to let you know cause Im elated!!! Thanks Jill > > > > > > Here are the messages received yesterday!

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