Re: [Histonet] Fwd: Plants
A canary? Well, I know what you used that for...how did that work out for you? Actually, I know the answer because you're alive. EH&S should really look into this option, screw the badges... Emily The whole point of this country is if you want to eat garbage, balloon up to 600 pounds and die of a heart attack at 43, you can! You are free to do so. To me, that’s beautiful. --Ron Swanson On Fri, May 11, 2012 at 1:32 PM, William wrote: > I have had plants in a number of labs. Could be against the rules, but I > never saw it. I even had a canary in one lab - pretty sure that is against > the rules. > > Will Chappell > > Sent from my iPhone > > On May 11, 2012, at 1:29 PM, "Behnaz Sohrab" wrote: > > > > > I was told by infectious control person that plants are not allowed in > the lab?? IS this true? any experience with this? > > Thank you, Behnaz > > ___ > > 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 > ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Fwd: Plants
Yeah but they used to use canaries in mines to warn of toxic levels of gases; having one in a histo lab might be a VERY good idea! -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of William Sent: Friday, May 11, 2012 12:33 PM To: Behnaz Sohrab Cc: Subject: Re: [Histonet] Fwd: Plants I have had plants in a number of labs. Could be against the rules, but I never saw it. I even had a canary in one lab - pretty sure that is against the rules. Will Chappell Sent from my iPhone On May 11, 2012, at 1:29 PM, "Behnaz Sohrab" wrote: > > I was told by infectious control person that plants are not allowed in the lab?? IS this true? any experience with this? > Thank you, Behnaz > ___ > 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 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Fwd: Plants
I've always had at least one; makes the day more tolerable. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Behnaz Sohrab Sent: Friday, May 11, 2012 12:30 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Fwd: Plants I was told by infectious control person that plants are not allowed in the lab?? IS this true? any experience with this? Thank you, Behnaz ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Xylene Substitute for Counterstain Clearing
You are also likely to have spheres dissolve in toluene based mounting media. Aqueous media may be the answer unless the neutral red runs out of the tissue in the aqueous environment. Hard to get the best of both worlds if dye runs in aqueous media and spheres dissolve in solvent based . Good luck! Gayle Callis -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa Sent: Friday, May 11, 2012 12:23 PM To: histonet@lists.utsouthwestern.edu; Andrew Coleman Subject: Re: [Histonet] Xylene Substitute for Counterstain Clearing After staining dry the sections in an oven at 60ºC for 10 minutes. When completely dried, coverslip as usual. Beware of the mounting medium solvent because it may contain xylene as well. Use one mounting medium without xylene. René J. --- On Fri, 5/11/12, Andrew Coleman wrote: From: Andrew Coleman Subject: [Histonet] Xylene Substitute for Counterstain Clearing To: histonet@lists.utsouthwestern.edu Date: Friday, May 11, 2012, 12:25 PM Hi all, We are performing a neutral red counterstain on tissue sections containing colored polystyrene microspheres. The spheres are inert to alcohol, but are washed out when we clear with xylene to coverslip. The spheres are also supposedly soluble in DMF, acetone, acetonitrile, chloroform and methylene chloride for what its worth. Is it reasonable to coverslip these slides in permanent mount without clearing with xylene after dehydrating the tissue? Or does anyone know of a substitute clearing agent with chemical properties dissimilar enough from xylene that might be worth trying instead? Thanks, Andrew ___ 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 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Fwd: Plants
Hate to say it, but yes plants are considered infectious. Thats why you cant take them in ICU's either. I guess the mold or bacterias can grow on them. Most places let this slide, but some dont. Good luck! From: William To: Behnaz Sohrab Cc: "" Sent: Friday, May 11, 2012 1:32 PM Subject: Re: [Histonet] Fwd: Plants I have had plants in a number of labs. Could be against the rules, but I never saw it. I even had a canary in one lab - pretty sure that is against the rules. Will Chappell Sent from my iPhone On May 11, 2012, at 1:29 PM, "Behnaz Sohrab" wrote: > > I was told by infectious control person that plants are not allowed in the > lab?? IS this true? any experience with this? > Thank you, Behnaz > ___ > 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 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Fwd: Plants
I keep a pothos and spider plant in my lab. EH&S has never complained, though I can't say one way or another if it's technically allowed. While my plants are mostly just decorative (I don't think I have enough of them to make much of a difference), it doesn't hurt that they may be filtering our air somewhat. NASA compiled a list of air-filtering plants that can eliminate significant amounts of formaldehyde, xylene, benzene, etc. (Source: http://en.wikipedia.org/wiki/List_of_air-filtering_plants). Lucie UCSD Dept. of Pathology On Friday, May 11, 2012, Victoria Baker wrote: > It's probably more toxic for the plants, but I like having them and no one > has told me I had to remove them. Ivy's are the most sturdy and the green > color just perks up things. > On Fri, May 11, 2012 at 1:29 PM, Behnaz Sohrab wrote: > > > > > I was told by infectious control person that plants are not allowed in > the > > lab?? IS this true? any experience with this? > > Thank you, Behnaz > > > > ___ > > 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 > ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] paraffin melting in VIP
When it is time to exchange reagents, the paraffin is the first thing we do because of the melting time required. We fill up the bin and place it in the oven until there is room to add more wax pellets - we do not stuff it in, but leave it rather loose. We do this about six times during the day until the bin is full. The paraffin pellets are not "cold" and there is a lot of residual heat in the oven due to the three hot wax bins already at temperature, so I am not sure how much "stress" this places on the heating elements. Tresa -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Gudrun Lang Sent: Friday, May 11, 2012 11:59 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] paraffin melting in VIP HI! A question for those, who melt the paraffin directly in the VIP. How long does it take to melt the pellets in the VIP-oven? Thanks Gudrun ___ 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
AW: [Histonet] paraffin melting in VIP
Thanks for your kind responses! Gudrun -Ursprüngliche Nachricht- Von: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von Gudrun Lang Gesendet: Freitag, 11. Mai 2012 19:59 An: histonet@lists.utsouthwestern.edu Betreff: [Histonet] paraffin melting in VIP HI! A question for those, who melt the paraffin directly in the VIP. How long does it take to melt the pellets in the VIP-oven? Thanks Gudrun ___ 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
RE: [Histonet] paraffin melting in VIP
This is probably a best case scenario, but for labs like the one I am currently in I melt it in the processor. My lab doesn't have the funds to buy me a melting pot (I have had them in all my other labs, just don't know what they are technically called). To answer your question it usually takes overnight and it's melted, but sometimes I end up having to add a little more to get to top off level, that takes a couple hours. Good Luck!! Sarah Goebel-Dysart, BA, HT(ASCP) Histotechnologist Mirna Therapeutics 2150 Woodward Street Suite 100 Austin, Texas 78744 (512)901-0900 ext. 6912 -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa Sent: Friday, May 11, 2012 1:28 PM To: histonet@lists.utsouthwestern.edu; gu.l...@gmx.at Subject: Re: [Histonet] paraffin melting in VIP Regardless of the time it takes or of how many people do it, melting the paraffin directly in the VIP should not be done because it causes the heating elements to work extra reducing their useful life. They are quite expensive to replace!. Melt the paraffin outside the VIP and use the VIP only to keep the melted paraffin at the temperature you desire. René J. --- On Fri, 5/11/12, Gudrun Lang wrote: From: Gudrun Lang Subject: [Histonet] paraffin melting in VIP To: histonet@lists.utsouthwestern.edu Date: Friday, May 11, 2012, 1:58 PM HI! A question for those, who melt the paraffin directly in the VIP. How long does it take to melt the pellets in the VIP-oven? Thanks Gudrun ___ 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 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] paraffin melting in VIP
I agree Rene! I also believe Sakura recommends not putting paraffin flakes directly in the containers. On Fri, May 11, 2012 at 2:27 PM, Rene J Buesa wrote: > Regardless of the time it takes or of how many people do it, melting the > paraffin directly in the VIP should not be done because it causes the > heating elements to work extra reducing their useful life. They are quite > expensive to replace!. > Melt the paraffin outside the VIP and use the VIP only to keep the melted > paraffin at the temperature you desire. > René J. > > --- On Fri, 5/11/12, Gudrun Lang wrote: > > > From: Gudrun Lang > Subject: [Histonet] paraffin melting in VIP > To: histonet@lists.utsouthwestern.edu > Date: Friday, May 11, 2012, 1:58 PM > > > HI! > > A question for those, who melt the paraffin directly in the VIP. How long > does it take to melt the pellets in the VIP-oven? > > > > Thanks > > Gudrun > > ___ > 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 > -- Jen Campbell, HT(ASCP) Supervisor of Technical Services Muhlbauer Dermatopathology Laboratory 61 Monroe Avenue, Ste B Pittsford NY 14534 P: 585.586.5166 F: 585.586.3137 IMPORTANT NOTICE: This e-mail and any attachments may contain confidential or sensitive information which is, or may be, legally privileged or otherwise protected by law from further disclosure. It is intended only for the addressee. If you received this in error or from someone who was not authorized to send it to you, please do not distribute, copy or use it or any attachments. Please notify the sender immediately by reply e-mail and delete this from your system. Thank you for your cooperation. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] paraffin melting in VIP
Regardless of the time it takes or of how many people do it, melting the paraffin directly in the VIP should not be done because it causes the heating elements to work extra reducing their useful life. They are quite expensive to replace!. Melt the paraffin outside the VIP and use the VIP only to keep the melted paraffin at the temperature you desire. René J. --- On Fri, 5/11/12, Gudrun Lang wrote: From: Gudrun Lang Subject: [Histonet] paraffin melting in VIP To: histonet@lists.utsouthwestern.edu Date: Friday, May 11, 2012, 1:58 PM HI! A question for those, who melt the paraffin directly in the VIP. How long does it take to melt the pellets in the VIP-oven? Thanks Gudrun ___ 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
Re: [Histonet] Xylene Substitute for Counterstain Clearing
After staining dry the sections in an oven at 60ºC for 10 minutes. When completely dried, coverslip as usual. Beware of the mounting medium solvent because it may contain xylene as well. Use one mounting medium without xylene. René J. --- On Fri, 5/11/12, Andrew Coleman wrote: From: Andrew Coleman Subject: [Histonet] Xylene Substitute for Counterstain Clearing To: histonet@lists.utsouthwestern.edu Date: Friday, May 11, 2012, 12:25 PM Hi all, We are performing a neutral red counterstain on tissue sections containing colored polystyrene microspheres. The spheres are inert to alcohol, but are washed out when we clear with xylene to coverslip. The spheres are also supposedly soluble in DMF, acetone, acetonitrile, chloroform and methylene chloride for what its worth. Is it reasonable to coverslip these slides in permanent mount without clearing with xylene after dehydrating the tissue? Or does anyone know of a substitute clearing agent with chemical properties dissimilar enough from xylene that might be worth trying instead? Thanks, Andrew ___ 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
Re: [Histonet] Xylene Substitute for Counterstain Clearing
I think that it is called Crystal Mount - but apply to section, allow to harden dip slide in clearing media and coverslip. I know that there must be others out there as well. Good Luck On Fri, May 11, 2012 at 12:25 PM, Andrew Coleman wrote: > Hi all, > > We are performing a neutral red counterstain on tissue sections > containing colored polystyrene microspheres. The spheres are inert to > alcohol, but are washed out when we clear with xylene to coverslip. > The spheres are also supposedly soluble in DMF, acetone, acetonitrile, > chloroform and methylene chloride for what its worth. > > Is it reasonable to coverslip these slides in permanent mount without > clearing with xylene after dehydrating the tissue? Or does anyone know > of a substitute clearing agent with chemical properties dissimilar > enough from xylene that might be worth trying instead? > > Thanks, > > Andrew > > ___ > 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
Re: [Histonet] Fwd: Plants
It's probably more toxic for the plants, but I like having them and no one has told me I had to remove them. Ivy's are the most sturdy and the green color just perks up things. On Fri, May 11, 2012 at 1:29 PM, Behnaz Sohrab wrote: > > I was told by infectious control person that plants are not allowed in the > lab?? IS this true? any experience with this? > Thank you, Behnaz > > ___ > 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
[Histonet] paraffin melting in VIP
HI! A question for those, who melt the paraffin directly in the VIP. How long does it take to melt the pellets in the VIP-oven? Thanks Gudrun ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Xylene Substitute for Counterstain Clearing
Andrew You could use Clearium from Leica. Clearium can either be coverslipped from xylene or isopropyl alcohol. Drying time from isopropyl is longer then xylene. Cindy Cindy Pyse, CLT, HT (ASCP) Laboratory Manager X-Cell Laboratories 716-250-9235 etx. 232 e-mail cp...@x-celllab.com -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Andrew Coleman Sent: Friday, May 11, 2012 12:25 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Xylene Substitute for Counterstain Clearing Hi all, We are performing a neutral red counterstain on tissue sections containing colored polystyrene microspheres. The spheres are inert to alcohol, but are washed out when we clear with xylene to coverslip. The spheres are also supposedly soluble in DMF, acetone, acetonitrile, chloroform and methylene chloride for what its worth. Is it reasonable to coverslip these slides in permanent mount without clearing with xylene after dehydrating the tissue? Or does anyone know of a substitute clearing agent with chemical properties dissimilar enough from xylene that might be worth trying instead? Thanks, Andrew ___ 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
Re: [Histonet] Fwd: Plants
I have had plants in a number of labs. Could be against the rules, but I never saw it. I even had a canary in one lab - pretty sure that is against the rules. Will Chappell Sent from my iPhone On May 11, 2012, at 1:29 PM, "Behnaz Sohrab" wrote: > > I was told by infectious control person that plants are not allowed in the > lab?? IS this true? any experience with this? > Thank you, Behnaz > ___ > 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
[Histonet] Fwd: Plants
I was told by infectious control person that plants are not allowed in the lab?? IS this true? any experience with this? Thank you, Behnaz ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Xylene Substitute for Counterstain Clearing
Andrew There are aqueous permanent mounting medias such as Advantage Permanent Mounting Media from Accurate Chemical NB300A (516) 333-2221 its been years since I used it but it does work on some applications. Liz Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC Manager Premier Laboratory, LLC PO Box 18592 Boulder, CO 80308-1592 (303) 682-3949 office (303) 682-9060 fax (303) 881-0763 cell www.premierlab.com Ship to address: 1567 Skyway Drive, Unit E Longmont, CO 80504 -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Andrew Coleman Sent: Friday, May 11, 2012 10:25 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Xylene Substitute for Counterstain Clearing Hi all, We are performing a neutral red counterstain on tissue sections containing colored polystyrene microspheres. The spheres are inert to alcohol, but are washed out when we clear with xylene to coverslip. The spheres are also supposedly soluble in DMF, acetone, acetonitrile, chloroform and methylene chloride for what its worth. Is it reasonable to coverslip these slides in permanent mount without clearing with xylene after dehydrating the tissue? Or does anyone know of a substitute clearing agent with chemical properties dissimilar enough from xylene that might be worth trying instead? Thanks, Andrew ___ 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
[Histonet] Xylene Substitute for Counterstain Clearing
Hi all, We are performing a neutral red counterstain on tissue sections containing colored polystyrene microspheres. The spheres are inert to alcohol, but are washed out when we clear with xylene to coverslip. The spheres are also supposedly soluble in DMF, acetone, acetonitrile, chloroform and methylene chloride for what its worth. Is it reasonable to coverslip these slides in permanent mount without clearing with xylene after dehydrating the tissue? Or does anyone know of a substitute clearing agent with chemical properties dissimilar enough from xylene that might be worth trying instead? Thanks, Andrew ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Re. Grossing Cassette Baskets
You can get the old-style sakura baskets from this company. These are the ones in which the plastic cassettes lay on their sides. They are about half the price. * http://store.techonebiomedical.com/store/ We sell the old style Sakura baskets. We have the 50 and 100 cassette models. We also sell a 150 cassette deluxe model. Thanks Matt -- Matthew Mincer Tech One Biomedical Services 159 N Marion Street, PMB163 Oak Park, IL 60301 (708) 383-6040 X 10 fax (708) 383-6045 cell (708) 822-3738 -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mitchell Wan Sent: Thursday, May 10, 2012 3:57 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Re. Grossing Cassette Baskets Hi James, I am interested in locating some baskets as well. I am tempted to go to a local metal works shop and ask them to make some stainless steel ones for myself. It will be approx. 1/10 of the price. Regards Mitchell Wan InfinityPATH Pty Ltd M: 0418 745 750 P: 07 3123 F: 07 3123 8889 E: mitchell@infinitypath.com.au W: www.infinitypath.com.au Does anybody know where we can purchase wire or plastic tissue cassette baskets for our grossing stations. We are looking for baskets that will keep the cassettes in line similar to the old VIP 3000 metal baskets with dividers. In our workflow we later transfer the cassettes to processing baskets. (Looked into purchasing more processing baskets, but at 400-500 a basket that doesn't seem to feasible.) Surely someone has old wire baskets or new plastic ones. Thanks for your help. James Vickroy BS, HT(ASCP) Surgical and Autopsy Pathology Technical Supervisor Memorial Medical Center 217-788-4046 ___ 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
Re: [Histonet] cryptosopridia
Yes, most testing is performed in the Microbiology Laboratory; however, I have an IHC test for formalin-fixed, paraffin-embedded tissue. Richard Richard W. Cartun, MS, PhD Director, Histology & Immunopathology Director, Biospecimen Collection Programs Assistant Director, Anatomic Pathology Hartford Hospital 80 Seymour Street Hartford, CT 06102 (860) 545-1596 Office (860) 545-2204 Fax >>> "Webb, Dorothy L" 5/11/2012 10:11 AM >>> What stain is anyone using for cryptosporidia in histology?? I thought this was more of a microbiology test. Could use some help please!! Thanks, Dorothy Webb This e-mail and any files transmitted with it are confidential and are intended solely for the use of the individual or entity to whom they are addressed. If you are not the intended recipient or the individual responsible for delivering the e-mail to the intended recipient, please be advised that you have received this e-mail in error and that any use, dissemination, forwarding, printing, or copying of this e-mail is strictly prohibited. If you have received this communication in error, please return it to the sender immediately and delete the original message and any copy of it from your computer system. If you have any questions concerning this message, please contact the sender. Disclaimer R001.0 ___ 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
[Histonet] cryptosopridia
What stain is anyone using for cryptosporidia in histology?? I thought this was more of a microbiology test. Could use some help please!! Thanks, Dorothy Webb This e-mail and any files transmitted with it are confidential and are intended solely for the use of the individual or entity to whom they are addressed. If you are not the intended recipient or the individual responsible for delivering the e-mail to the intended recipient, please be advised that you have received this e-mail in error and that any use, dissemination, forwarding, printing, or copying of this e-mail is strictly prohibited. If you have received this communication in error, please return it to the sender immediately and delete the original message and any copy of it from your computer system. If you have any questions concerning this message, please contact the sender. Disclaimer R001.0 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
