[Histonet] FT position HISTOTECHNOLOGIST/IHC Delray Beach, FL
Hi Histonetters! We are looking for a full time licensed histotech here in our very busy Delray Florida Dermatology Lab. This is a permanent full time SECOND SHIFT (40 hours) position with benefits (medical/401k/vacation) and competitive pay. THIS IS A DRUG FREE WORKPLACE. Drug testing, background check and personality testing is required. ONLY SERIOUS INQURIES, please read EVERY qualification desired. Sorry, NO relocation assistance offered. Position available for training immediately. ***PLEASE NO HEAD HUNTERS/PLACEMENT SERVICES***!!! Email your resume to lengim...@leavittmgt.commailto:lengim...@leavittmgt.com if interested. *Full time position Mon-Fri 2p-10:30p (IMMUNOHISTOCHEMISTRY/SPECIALS department) *MUST be licensed as a FLORIDA HISTOTECHNOLOGIST (this is NOT negotiable) *EXPERIENCE WITH IHC A MUST! Leica (BOND) and Roche/Ventana equipment experience preferred *Must be able to multi-task special stains *MUST have at LEAST 2 years experience. Please DO NOT respond if you do not possess EXPERIENCE in this area! *must be confidant, quick learner, self motivated, reliable and a team player Kari M Simeone Histology/Immunohistochemistry Specialist Supervisor The information contained in this message and any attachments is intended only for the use of the individual or entity to which it is addressed, and may contain information that is privileged, confidential and exempt from disclosure under applicable law. If you have received this message in error, you are prohibited from copying, distributing or using the information. Please contact the sender immediately by return e-mail and delete the original message. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] pH measurements for tissue
Does anyone knows how to measure pH in tissue? Any help will be greatly appreciated. Thank you. Lin. Lin S. Bustamante, B.S., H.T.(ASCP) VIBS Histology Laboratory Supervisor College Of Veterinary Medicine Texas AM University College Station, Texas 77843-4458 Phone: (979) 845-3177 Fax: (979) 458-3499 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Specimen Triage
We are trying to create a consistent and efficient process for the triage of Radiology specimens going to Cytology, Surgical Pathology and Microbiology. I would really like to hear how other hospitals are handling this. Do you have a central drop off location and if so who handles this? Does radiology take them to the appropriate depts? Do you have the same process 8am-5pm and after hours or do you have different processes? I appreciate any feedback you are willing to give. Thanks, Dana -- The contents of this e-mail (and any attachments) are confidential, may be privileged and may contain copyright material. You may only reproduce or distribute material if you are expressly authorized by us to do so. If you are not the intended recipient, any use, disclosure or copying of this email (and any attachments) is unauthorized. If you have received this e-mail in error, please notify the sender and immediately delete this e-mail and any copies of it from your system. == ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Beta 2 adrenergic receptor IHC
Does anyone have any recommendations for antibodies and or is aware of specific issues/limitations for Beta 2 adrenergic receptor IHC? Working with murine WT KO, PFA fixed frozen sections. Either IF or chromogenic are options...Open to any guidance or suggestions ?Thanks ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] FT NIGHT (3rd shift) POSITION DELRAY BCH FL
Hi Histonetters! We are looking for a full time licensed histotech here in our very busy Delray Florida Dermatology Lab. This is a permanent full time NIGHT SHIFT (40 hours) position with benefits (medical/401k/vacation) and shift differential. THIS IS A DRUG FREE WORKPLACE. Background check, personality test and drug test will be necessary. Sorry, no relocation assistance provided. ***PLEASE NO HEAD HUNTERS/PLACEMENT SERVICES***!!! Email your resume to lengim...@leavittmgt.commailto:lengim...@leavittmgt.com if interested. *full time position Mon-Fri or Sun-Thurs 6PM-2:30AM *MUST be licensed as a FL HISTOTEHCNOLOGIST ONLY (will be working solo) *MUST have at LEAST 2 years experience (dermatology preferred) Please DO NOT respond if no EXPERIENCE! *VERY proficient in embedding and microtomy *must be self motivated, reliable and a team player *knowledge in operating Ventana and Leica equipment desired (not necessary) *some IHC experience preferred Kari M Simeone 561.819.6517 fax ksime...@leavittmgt.commailto:ksime...@leavittmgt.com The information contained in this message and any attachments is intended only for the use of the individual or entity to which it is addressed, and may contain information that is privileged, confidential and exempt from disclosure under applicable law. If you have received this message in error, you are prohibited from copying, distributing or using the information. Please contact the sender immediately by return e-mail and delete the original message. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Removing paraffin sections from glass slides
Why shouldn't the slide surfaces remain positively charged after removing the sections? Water, alcohol and xylene are all routinely used, and don't impair electrostatic forces that help to hold the sections on the slide. The positively charged surface is not a coating that can be washed or rubbed off. Joyce Weems's suggested method did not involve anything that might react chemically with the cationic (amino-hydrocarbon) groups that are covalently bound to the polysilicate structure of the glass. See http://publish.uwo.ca/~jkiernan/adhesivs.htm John Kiernan Anatomy Cell Biology University of Western Ontario London, Canada = = = On 23/06/15, Jamal j.rowa...@alborglaboratories.com wrote: Dear Colleague I just want to remind you.. After all of that procedure of removing the paraffin sections from the positive charged slides. The slides will not be positive charged anymore and not suitable for IHC. Also the cost of the detergents and the chemicals which you used for removing the tissue section is more costly than the slides. Best Regards, Jamal M. Al Rowaihi Anatomic Pathology Supervisor | Al Borg Medical Laboratories | Mobile +966 503629832| j.rowa...@alborglaboratories.com Palestine St, Al Rajhi Building, P.O. Box 52817, Jeddah 21573, KSA | Phone: +966 12 670 0099 | Fax: +966 12 676 4984 | www.alborglaboratories.com -Original Message- From: Weems, Joyce K. [mailto:joyce.we...@emoryhealthcare.org] joyce.we...@emoryhealthcare.org] Sent: Monday, June 22, 2015 5:53 PM To: 'Coffey, Anna (NIH/NCI) [C]'; histonet@lists.utsouthwestern.edu Subject: Re: [Histonet] Removing paraffin sections from glass slides This is what I would do... Soak the coverslip off in xylene Either - rehydrate back to water and just wipe the tissue off - then dip the slides in absolute and let dry.. OR - air dry out of xylene and wipe off with a wet gauze - then do the alcohol dip Whichever worked best. Just my 2 cents.. Happy Monday!! Joyce Weems Pathology Manager 678-843-7376 Phone 678-843-7831 Fax joyce.we...@emoryhealthcare.org www.saintjosephsatlanta.org 5665 Peachtree Dunwoody Road Atlanta, GA 30342 This e-mail, including any attachments is the property of Saint Joseph's Hospital and is intended for the sole use of the intended recipient(s). It may contain information that is privileged and confidential. Any unauthorized review, use, disclosure, or distribution is prohibited. If you are not the intended recipient, please delete this message, and reply to the sender regarding the error in a separate email. -Original Message- From: Coffey, Anna (NIH/NCI) [C] [mailto:anna.cof...@nih.gov] anna.cof...@nih.gov] Sent: Monday, June 22, 2015 10:25 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Removing paraffin sections from glass slides Hello, I'm wondering if anyone has experience removing dried unstained paraffin sections from charged glass slides. I don't need to preserve the sections, just want to reuse the slides. Thanks! Anna Anna Coffey, MS, HTL(ASCP)CM Histotechnologist Center for Advanced Preclinical Research Frederick National Laboratory for Cancer Research Leidos Biomedical Research, Inc. Bld 539, 224 Frederick, Maryland 21702 anna.cof...@nih.gov 301-846-1730 ___ 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 recipient(s) and may contain confidential and privileged information. If the reader of this message is not the intended recipient, you are hereby notified that any dissemination, distribution or copying of this message (including any attachments) is strictly prohibited. If you have received this message in error, please contact the sender by reply e-mail message and destroy all copies of the original message (including attachments). ___ 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] de-waxing protocol on instruments just fact finding
Rachel, We dewax off line. We use the same protocol that we do for any other staining; 3 min in 3 changes of xylene (we use a xylene substitute though), 3 min in 2 changes of 100% alcohol and one 3 min in 95%. We use BioCare's IntelliPath immuno stainer. It is a completely open system. All of the sales reps, support techs, and service tech have always been very open and willing to help in any way to provide information and support for this stainer. If by dewaxing you are also referring to off line antigen retrieval, we use the pressure cooker that BioCare has. You can use any retrieval solution you choose with it. If you need to use two different retrieval solutions you can fill your containers with two different retrieval reagents. I don't find that there is any difference in doing off line retrieval than on line retrieval. If I can answer any other questions please feel free to contact me. Linda Linda Blazek HT (ASCP) Manager/Supervisor GI Pathology of Dayton Digestive Specialists, Inc Phone: (937) 396-2623 Email: lbla...@digestivespecialists.com -Original Message- From: Rachel M Gonzalez [mailto:rac...@gbi-inc.com] Sent: Monday, June 22, 2015 5:21 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] de-waxing protocol on instruments just fact finding Hi Just beginning to look at instruments DAKO Ventana Leica. We may not have the budget but if we do However talking to the sales reps have been challenging as everything is proprietary. This is for research consideration so we will use an open instrument? Which instrument do you like better open? Does manual dewaxing affect the staining? Every rep says yes... but does it? What is the time for dewaxing when you start the instrument? What are the number of steps in the protocol? What is the waste generation like more or less than manual? Thanks for your help. Rachel ___ 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] Removing paraffin sections from glass slides
Dear Colleague I just want to remind you.. After all of that procedure of removing the paraffin sections from the positive charged slides. The slides will not be positive charged anymore and not suitable for IHC. Also the cost of the detergents and the chemicals which you used for removing the tissue section is more costly than the slides. Best Regards, Jamal M. Al Rowaihi Anatomic Pathology Supervisor | Al Borg Medical Laboratories | Mobile +966 503629832| j.rowa...@alborglaboratories.com Palestine St, Al Rajhi Building, P.O. Box 52817, Jeddah 21573, KSA| Phone: +966 12 670 0099 | Fax: +966 12 676 4984 | www.alborglaboratories.com -Original Message- From: Weems, Joyce K. [mailto:joyce.we...@emoryhealthcare.org] Sent: Monday, June 22, 2015 5:53 PM To: 'Coffey, Anna (NIH/NCI) [C]'; histonet@lists.utsouthwestern.edu Subject: Re: [Histonet] Removing paraffin sections from glass slides This is what I would do... Soak the coverslip off in xylene Either - rehydrate back to water and just wipe the tissue off - then dip the slides in absolute and let dry.. OR - air dry out of xylene and wipe off with a wet gauze - then do the alcohol dip Whichever worked best. Just my 2 cents.. Happy Monday!! Joyce Weems Pathology Manager 678-843-7376 Phone 678-843-7831 Fax joyce.we...@emoryhealthcare.org www.saintjosephsatlanta.org 5665 Peachtree Dunwoody Road Atlanta, GA 30342 This e-mail, including any attachments is the property of Saint Joseph's Hospital and is intended for the sole use of the intended recipient(s). It may contain information that is privileged and confidential. Any unauthorized review, use, disclosure, or distribution is prohibited. If you are not the intended recipient, please delete this message, and reply to the sender regarding the error in a separate email. -Original Message- From: Coffey, Anna (NIH/NCI) [C] [mailto:anna.cof...@nih.gov] Sent: Monday, June 22, 2015 10:25 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Removing paraffin sections from glass slides Hello, I'm wondering if anyone has experience removing dried unstained paraffin sections from charged glass slides. I don't need to preserve the sections, just want to reuse the slides. Thanks! Anna Anna Coffey, MS, HTL(ASCP)CM Histotechnologist Center for Advanced Preclinical Research Frederick National Laboratory for Cancer Research Leidos Biomedical Research, Inc. Bld 539, 224 Frederick, Maryland 21702 anna.cof...@nih.gov 301-846-1730 ___ 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 recipient(s) and may contain confidential and privileged information. If the reader of this message is not the intended recipient, you are hereby notified that any dissemination, distribution or copying of this message (including any attachments) is strictly prohibited. If you have received this message in error, please contact the sender by reply e-mail message and destroy all copies of the original message (including attachments). ___ 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] Antigen retrieval survey
Your 2 minutes would be better spent looking in an immunohistochemistry textbook. A small but excellent one is Polak, J.M. and Van Noorden, S. (1997). Introduction to Immunocytochemistry, 2nd ed. Royal Microscopical Society Microscopy Handbooks, 37. Oxford: BIOS Scientific Publications. You will find that there is an optimal technique of antigen retrieval for each antigen that has been critically studied. Some conditions (such as pH6, close to 100C for an hour) are OK for many antigens. Some require more alkaline solutions (eg pH9, more section losses!) and a few respond best to heating in a more acid (eg pH2) solution. With lower temperatures (eg 80C) longer times are generally needed. All sorts of chemicals have been included in antigen retrieval solutions, often without obvious reasons or explanations. There are published papers that compare retrieval conditions for antigens of importance in diagnostic pathology. Retrieval can sometimes be achieved without heating, as with proteolytic enzymes or 3M urea. With a survey you may find out which antigen retrieval methods are used by most of those who reply, but you will not learn anything about how to choose and use the methods, or why their discovery about 25 years ago was an important technological advance. Check out this classic paper with Web of Science, Scopus, or Google Scholar: Shi, S.-R., Key, M.E. and Kalra, K.L. (1991). Antigen retrieval in formalin-fixed, paraffin-embedded tissue: an enhancement method for immunohistochemical staining based on microwave oven heating of tissue sections. Journal of Histochemistry and Cytochemistry 39:741-748. The PDF can be downloaded for free. This paper has been cited by thousands of other publications. The titles of recent citing articles may help you find a good retrieval procedure for the antigen that you need to detect immunohistochemically. John Kiernan UWO, London, Canada = = = On 23/06/15, Craig volle...@gmail.com wrote: Hi, I am conducting a short 2 min survey for my science/business class examining current trends for antigen retrieval also known as heat induce epitope retrieval. Response will be greatly appreciated! https://www.surveymonkey.com/s/7989LKR Best, Craig Vollert Graduate Student Department of Pharmacological Pharmaceutical Sciences SR2 521B College of Pharmacy University of Houston ___ 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] Removing paraffin sections from glass slides
Hi Anna, You could deparaffinize/rehydrate to 10% (or so) bleach. Section(s) comes right off after ~1-60 minutes (or so). Did this by accident (that was a bad day). Deparaffinzation via Rene J Buesa's DWS (http://www.histosearch.com/ADP7HistologyWithoutXylene.pdf) method, or simply quick (20 seconds each) xylene/alcohol/water should suffice. I don't know what bleach will do to the charge on your plus slide, but I assume you should Clean with acid to be useful(?). I have been queried about reusing slides from several physicians in the past, but never been organized enough to try it. Good luck, in whatever you are doing. Hugh Hawaii -- Date: Mon, 22 Jun 2015 14:24:50 + From: Coffey, Anna (NIH/NCI) [C] anna.cof...@nih.gov To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu Subject: [Histonet] Removing paraffin sections from glass slides Message-ID: 5c3e10119a1b824fbe92b08279f74a9102597...@msgb10.nih.gov Content-Type: text/plain; charset=us-ascii Hello, I'm wondering if anyone has experience removing dried unstained paraffin sections from charged glass slides. I don't need to preserve the sections, just want to reuse the slides. Thanks! Anna Anna Coffey, MS, HTL(ASCP)CM Histotechnologist Center for Advanced Preclinical Research Frederick National Laboratory for Cancer Research Leidos Biomedical Research, Inc. Bld 539, 224 Frederick, Maryland 21702 anna.cof...@nih.gov 301-846-1730 -- Message: 5 Date: Mon, 22 Jun 2015 14:52:30 + From: Weems, Joyce K. joyce.we...@emoryhealthcare.org To: 'Coffey, Anna (NIH/NCI) [C]' anna.cof...@nih.gov, histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu Subject: Re: [Histonet] Removing paraffin sections from glass slides Message-ID: e3a4ebd57a691646bcced4aa5911a030011c747...@e14mbx12n.enterprise.emory.net Content-Type: text/plain; charset=us-ascii This is what I would do... Soak the coverslip off in xylene Either - rehydrate back to water and just wipe the tissue off - then dip the slides in absolute and let dry.. OR - air dry out of xylene and wipe off with a wet gauze - then do the alcohol dip Whichever worked best. Just my 2 cents.. Happy Monday!! Joyce Weems Pathology Manager 678-843-7376 Phone 678-843-7831 Fax joyce.we...@emoryhealthcare.org www.saintjosephsatlanta.org 5665 Peachtree Dunwoody Road Atlanta, GA 30342 This e-mail, including any attachments is the property of Saint Joseph's Hospital and is intended for the sole use of the intended recipient(s). It may contain information that is privileged and confidential. Any unauthorized review, use, disclosure, or distribution is prohibited. If you are not the intended recipient, please delete this message, and reply to the sender regarding the error in a separate email. -Original Message- From: Coffey, Anna (NIH/NCI) [C] [mailto:anna.cof...@nih.gov] Sent: Monday, June 22, 2015 10:25 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Removing paraffin sections from glass slides Hello, I'm wondering if anyone has experience removing dried unstained paraffin sections from charged glass slides. I don't need to preserve the sections, just want to reuse the slides. Thanks! Anna Anna Coffey, MS, HTL(ASCP)CM Histotechnologist Center for Advanced Preclinical Research Frederick National Laboratory for Cancer Research Leidos Biomedical Research, Inc. Bld 539, 224 Frederick, Maryland 21702 anna.cof...@nih.gov 301-846-1730 ___ 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 recipient(s) and may contain confidential and privileged information. If the reader of this message is not the intended recipient, you are hereby notified that any dissemination, distribution or copying of this message (including any attachments) is strictly prohibited. If you have received this message in error, please contact the sender by reply e-mail message and destroy all copies of the original message (including attachments). -- Subject: Digest Footer ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet -- End of Histonet Digest, Vol 139, Issue 22 * ___ Histonet mailing list Histonet@lists.utsouthwestern.edu
Re: [Histonet] Removing paraffin sections from glass slides
Ventana loves that excuse for stain failures They even made us flip our slides upside down to place the control on the slide then flip them around to place the section on the slide due to the electrostatic forces Additionally all slides had to be air dried then placed in slide boxes prior to use Crap I say! Sent from my iPhone On Jun 23, 2015, at 5:50 PM, John Kiernan jkier...@uwo.ca wrote: Why shouldn't the slide surfaces remain positively charged after removing the sections? Water, alcohol and xylene are all routinely used, and don't impair electrostatic forces that help to hold the sections on the slide. The positively charged surface is not a coating that can be washed or rubbed off. Joyce Weems's suggested method did not involve anything that might react chemically with the cationic (amino-hydrocarbon) groups that are covalently bound to the polysilicate structure of the glass. See http://publish.uwo.ca/~jkiernan/adhesivs.htm John Kiernan Anatomy Cell Biology University of Western Ontario London, Canada = = = On 23/06/15, Jamal j.rowa...@alborglaboratories.com wrote: Dear Colleague I just want to remind you.. After all of that procedure of removing the paraffin sections from the positive charged slides. The slides will not be positive charged anymore and not suitable for IHC. Also the cost of the detergents and the chemicals which you used for removing the tissue section is more costly than the slides. Best Regards, Jamal M. Al RowaihiAnatomic Pathology Supervisor | Al Borg Medical Laboratories | Mobile +966 503629832| j.rowa...@alborglaboratories.com Palestine St, Al Rajhi Building, P.O. Box 52817, Jeddah 21573, KSA | Phone: +966 12 670 0099 | Fax: +966 12 676 4984 | www.alborglaboratories.com -Original Message- From: Weems, Joyce K. [mailto:joyce.we...@emoryhealthcare.org] joyce.we...@emoryhealthcare.org] Sent: Monday, June 22, 2015 5:53 PM To: 'Coffey, Anna (NIH/NCI) [C]'; histonet@lists.utsouthwestern.edu Subject: Re: [Histonet] Removing paraffin sections from glass slides This is what I would do... Soak the coverslip off in xylene Either - rehydrate back to water and just wipe the tissue off - then dip the slides in absolute and let dry.. OR - air dry out of xylene and wipe off with a wet gauze - then do the alcohol dip Whichever worked best. Just my 2 cents.. Happy Monday!! Joyce Weems Pathology Manager 678-843-7376 Phone 678-843-7831 Fax joyce.we...@emoryhealthcare.org www.saintjosephsatlanta.org 5665 Peachtree Dunwoody Road Atlanta, GA 30342 This e-mail, including any attachments is the property of Saint Joseph's Hospital and is intended for the sole use of the intended recipient(s). It may contain information that is privileged and confidential. Any unauthorized review, use, disclosure, or distribution is prohibited. If you are not the intended recipient, please delete this message, and reply to the sender regarding the error in a separate email. -Original Message- From: Coffey, Anna (NIH/NCI) [C] [mailto:anna.cof...@nih.gov] anna.cof...@nih.gov] Sent: Monday, June 22, 2015 10:25 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Removing paraffin sections from glass slides Hello, I'm wondering if anyone has experience removing dried unstained paraffin sections from charged glass slides. I don't need to preserve the sections, just want to reuse the slides. Thanks! Anna Anna Coffey, MS, HTL(ASCP)CM Histotechnologist Center for Advanced Preclinical Research Frederick National Laboratory for Cancer Research Leidos Biomedical Research, Inc. Bld 539, 224 Frederick, Maryland 21702 anna.cof...@nih.gov 301-846-1730 ___ 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 recipient(s) and may contain confidential and privileged information. If the reader of this message is not the intended recipient, you are hereby notified that any dissemination, distribution or copying of this message (including any attachments) is strictly prohibited. If you have received this message in error, please contact the sender by reply e-mail message and destroy all copies of the original message (including attachments). ___ 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
[Histonet] Antigen retrieval survey
Hi, I am conducting a short 2 min survey for my science/business class examining current trends for antigen retrieval also known as heat induce epitope retrieval. Response will be greatly appreciated! https://www.surveymonkey.com/s/7989LKR Best, Craig Vollert Graduate Student Department of Pharmacological Pharmaceutical Sciences SR2 521B College of Pharmacy University of Houston ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
