Re: [Histonet] her 2 controls
Check out Histocyte controls, which are available on slides or blocks. One of their distributors is Cell Marque: http://www.cellmarque.com/cms/histocyte/HER2.php Their Her2 control include 0, 1+, 2+, and 3+. Michael J. Dessoye, M.S. | Histology/Toxicology/Special Chemistry Supervisor | Commonwealth Health Laboratory Services | mjdess...@commonwealthhealth.net | 575 N. River Street | Wilkes Barre, PA 18764 | Tel: 570-552-1432 | Fax: 570-552-1484 -Original Message- From: Nirmala Srishan [mailto:sris...@mail.holyname.org] Sent: Thursday, April 18, 2019 12:15 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] her 2 controls Can someone suggest a company to purchase good Her 2 control slides. Preferably multi-tissue controls with +1,+2,+3. Thanks in advance. Nirmala Srishan Supervisor Histology Department of Pathology and Laboratory Medicine Holy Name Medical Center Teaneck, NJ Office: 201 541 6328 Lab: 201 833 3023 sris...@holyname.org Holy Name Medical Center is ranked among the top hospitals in the nation for patient care, clinical performance and workplace excellence. Click here to learn more. Warning: The information contained in this message is privileged and CONFIDENTIAL and is intended only for the use of the addressee above. If you are not the intended recipient, you are hereby notified that any disclosure, copying, distribution, or taking of any action in reliance on the content of this message is strictly prohibited. If you have received this communication in error, please notify the sender by replying to this message, and then delete it from your system. ** Disclaimer: This electronic message may contain information that is Proprietary, Confidential, or legally privileged or protected. It is intended only for the use of the individual(s) and entity named in the message. If you are not an intended recipient of this message, please notify the sender immediately and delete the material from your computer. Do not deliver, distribute or copy this message and do not disclose its contents or take any action in reliance on the information it contains. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] her 2 controls
I recommend that you e-mail these two gentlemen (both are super helpful) and they can put you in touch with your local distributor. Both their companies have HER2 controls plus controls for many other analytes. mr...@statlab.com (Mark Rees) colin.trist...@histocyte.com John www.ciqc.ca ‐‐‐ Original Message ‐‐‐ On Thursday, April 18, 2019 9:15 AM, Nirmala Srishan via Histonet wrote: > Can someone suggest a company to purchase good Her 2 control slides. > Preferably multi-tissue controls with +1,+2,+3. > Thanks in advance. > > Nirmala Srishan > Supervisor Histology > Department of Pathology and Laboratory Medicine > Holy Name Medical Center Teaneck, NJ > Office: 201 541 6328 > Lab: 201 833 3023 > sris...@holyname.org > > Holy Name Medical Center is ranked among the top hospitals in the nation > for patient care, clinical performance and workplace excellence. > Click here to learn more. > > Warning: The information contained in this message is privileged and > CONFIDENTIAL and is intended only for the use of the addressee above. If > you are not the intended recipient, you are hereby notified that any > disclosure, copying, distribution, or taking of any action in reliance on > the content of this message is strictly prohibited. If you have received > this communication in error, please notify the sender by replying to this > message, and then delete it from your system. > > 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] her 2 controls
Can someone suggest a company to purchase good Her 2 control slides. Preferably multi-tissue controls with +1,+2,+3. Thanks in advance. Nirmala Srishan Supervisor Histology Department of Pathology and Laboratory Medicine Holy Name Medical Center Teaneck, NJ Office: 201 541 6328 Lab: 201 833 3023 sris...@holyname.org Holy Name Medical Center is ranked among the top hospitals in the nation for patient care, clinical performance and workplace excellence. Click here to learn more. Warning: The information contained in this message is privileged and CONFIDENTIAL and is intended only for the use of the addressee above. If you are not the intended recipient, you are hereby notified that any disclosure, copying, distribution, or taking of any action in reliance on the content of this message is strictly prohibited. If you have received this communication in error, please notify the sender by replying to this message, and then delete it from your system. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Her 2 Control
Hey Scott - Our interpretation of CAP requirements for IHC Controls is the same as yours. Our Her2 control is a microarray with 3+ case and a piece of normal skin to serve as our negative tissue control. If you have normal breast tissue adjacent to your tumor control, that can also serve as a negative tissue control, but your procedure has to state it as such. Our control tissue are 5mm punches of solid tumor, so we just add a punch of normal skin. I hope this helps, but sometimes, it's just not worth the argument. Terri L. Braud, HT(ASCP) Anatomic Pathology Supervisor Laboratory Holy Redeemer Hospital 1648 Huntingdon Pike Meadowbrook, PA 19046 ph: 215-938-3689 fax: 215-938-3874 Care, Comfort, and Heal Message: 2 Date: Tue, 21 Nov 2017 21:05:51 + From: "Lindrud, Scott" Subject: [Histonet] Negative IHC Control for Her2 Hi All, We are having an internal debate regarding Her2 IHC control tissue in our lab. We run a MTA (multi tissue array) consisting of 0+, 1+, 2+, and 3+ Her2 staining tissue taken from lumpectomy/resection cases. I'm in the process of searching for more tissue to use in future control blocks and it can be difficult to find tissue that is 0+ and 3+. I've discussed this with our pathologist in charge of Histology and he says that we don't need to run all 4 of the cores as controls. He says all we need to run is a positive control and a negative control. He says the positive control could be a 2+ or 3+ and the negative control could be either a 0+ OR a 1+. I respectfully disagreed with him and said the negative control is not meant for accessing staining interpretation but to verify the sensitivity and specificity of the actual antibody-antigen reaction. I said a 1+ is still staining the tissue where there is no staining in a 0+ reaction. The 1+ is not a negative staining reaction, but a negative interpretation. The pathologist says I'm wrong. The CAP in its checklist says "It is also important to assess the specificity of each antibody by a negative tissue control, which must show no staining of tissues known to lack the antigen".To me, a 1+ Her2 staining reaction shows that that tissue has antigen and should not be used as a negative control. So, after saying all that, can/should 1+ Her2 breast tissue be used as a negative tissue control? Seems pretty straight forward to me, but I'm just a Cytotechnologist/Histotech. Thanks for any input! Scott Scott A. Lindrud, MLS(ASCP)CM CTCM Histopathology Technical Specialist/Cytotechnologist Rice Memorial Hospital 301 Becker Ave SW Willmar, MN 56201 WP(320)231-4406 Fax(320)231-4861 scott.lind...@rice.willmar.mn.us "This e-mail transmission is for the sole use of the intended recipient(s) and may contain confidential and privileged information. Any unauthorized review, use, disclosure, or distribution violates confidentiality and privacy laws and is prohibited. If you are not the intended recipient, please notify the sender immediately and delete all copies of the message. Thank you." -- Message: 3 Date: Wed, 22 Nov 2017 16:02:21 + (UTC) From: Rene J Buesa To: "Lindrud, Scott" , "histonet@lists.utsouthwestern.edu" Subject: Re: [Histonet] Negative IHC Control for Her2 Message-ID: <800857894.1231622.1511366541...@mail.yahoo.com> Content-Type: text/plain; charset=UTF-8 You are right but, your point is?Regardless, the pathologist is the responsible for his/her diagnosis/interpretation and the liability is his/hers.Remember that for us histotechs, our "client" is the pathologist (always remembering the patient behind the whole process) and our essential duty is to provide the pathologist what s/he needs to being able to make the best and more accurate diagnosis.Follow his/her instructions and your life will be much simpler and less stressful.Ren? On Tuesday, November 21, 2017 4:21 PM, "Lindrud, Scott via Histonet" wrote: Hi All, We are having an internal debate regarding Her2 IHC control tissue in our lab.? We run a MTA (multi tissue array) consisting of 0+, 1+, 2+, and 3+ Her2 staining tissue taken from lumpectomy/resection cases.? I'm in the process of searching for more tissue to use in future control blocks and it can be difficult to find tissue that is 0+ and 3+. I've discussed this with our pathologist in charge of Histology and he says that we don't need to run all 4 of the cores as controls.? He says all we need to run is a positive control and a negative control.? He says the positive control could be a 2+ or 3+ and the negative control could be either a 0+ OR a 1+. I respectfully disagreed with him and said the negative control is not meant for accessing staining interpretation but to verify the sensitivity and specificity of the actual antibody-antigen reaction.? I said a 1+ is still staining the tissue where there is no staining in a 0+ reaction.? The 1+ is not a negative stai
[Histonet] Her-2 Bond issues
Robert, We had a similar problem with our Bond. It was a calibration issue. It was only noticeable with our more "delicate" antibodies. I would call for service. Sara McCabe, HT(ASCP) DuBois Regional Medical Center This email and any attached files are confidential and intended solely for the intended recipient(s). If you are not the named recipient you should not read, distribute, copy or alter this email. Any views or opinions expressed in this email are those of the author and do not represent those of the company. Warning: Although precautions have been taken to make sure no viruses are present in this email, the company cannot accept responsibility for any loss or damage that arise from the use of this email or attachments. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] HER-2
I would suggest that you send several of your own cases to a reference lab that reads tons of them and see what numbers they report. Then compare the two results. 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: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Wilson A Sent: Friday, February 01, 2013 9:52 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] HER-2 Hi, Our pathologists are concerned we may be reporting too many 2+ HER2’s. Can someone help with this? Thanks, Wilson ___ 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
Re: [Histonet] HER-2
Many pathologists, if they have any doubt about the score will just say that it is 2+ so that its gets HER2 by FISH which is considered the best method for determining HER2 status. Even if by the scoring criteria it is a 1+ but the intensity is a little stronger than normal (but maybe basolateral or not complete staining) they just go with 2+. Sometimes its high grade 1+ and it doesn't quite meet the 2+ staining criteria and they call it 2+ too. If these things are happening enough it could mean calling more 2+ cases. They don't always follow the scoring criteria to the letter. We use digital image analysis for HER2 IHC scoring and the computer is pretty right on (matches with FISH), but sometimes the pathologist will change the score in the report to 2+ even though it's a 1+ by the computer. There is one pathologist in particular who doesn't believe in the computer reading the HER2 score and is trying very hard to find cases that are positive by FISH but that the computer is calling the IHC 1+. He also requests FISH on some 3+ cases to try and find any over-calling by the computer. The thought of a woman getting a toxic drug needlessly really bothers him. So without Wilson posting more info there's not much help that I think anyone can offer. This is stain that has to be validated more extensively than others, so the protocol shouldn't just be tweaked. How do the controls look? Was there any lot to lot variation? Lots of questions.. Mark On Tue, Feb 5, 2013 at 12:49 PM, Rene J Buesa wrote: > Yes, that is sometimes a common occurrence amongst pathologists, BUT those > differences have to be solved in conference before issuing the report. > Difficult cases (at least at my hospital) are reviewed in conference, > I agree with you: your protocol (specially if it is based on DAKO'sprotocol) > should remain as is. > The diagnosis differences should not determine a change. > René J. > > *From:* Mark Tarango > *To:* Wilson A > *Cc:* "histonet@lists.utsouthwestern.edu" < > histonet@lists.utsouthwestern.edu> > *Sent:* Tuesday, February 5, 2013 2:24 PM > *Subject:* Re: [Histonet] HER-2 > > I'd be interested to know if all your pathologists agree that the 2+ cases > are 2+. Is it possible that one of the pathologists is calling more cases > as 2+ than the rest? I would have a lot of questions before modifying the > staining protocol. It would be helpful you posted more info. > > Mark T. > > On Fri, Feb 1, 2013 at 6:52 PM, Wilson A wrote: > > > > >Hi, > > Our pathologists are concerned we may be reporting too many 2+ > > HER2’s. Can someone help with this? > > > > Thanks, > >Wilson > > ___ > > 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] HER-2
Yes, that is sometimes a common occurrence amongst pathologists, BUT those differences have to be solved in conference before issuing the report. Difficult cases (at least at my hospital) are reviewed in conference, I agree with you: your protocol (specially if it is based on DAKO's protocol) should remain as is. The diagnosis differences should not determine a change. René J. From: Mark Tarango To: Wilson A Cc: "histonet@lists.utsouthwestern.edu" Sent: Tuesday, February 5, 2013 2:24 PM Subject: Re: [Histonet] HER-2 I'd be interested to know if all your pathologists agree that the 2+ cases are 2+. Is it possible that one of the pathologists is calling more cases as 2+ than the rest? I would have a lot of questions before modifying the staining protocol. It would be helpful you posted more info. Mark On Fri, Feb 1, 2013 at 6:52 PM, Wilson A wrote: > > Hi, > Our pathologists are concerned we may be reporting too many 2+ > HER2’s. Can someone help with this? > > Thanks, > Wilson > ___ > 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] HER-2
I'd be interested to know if all your pathologists agree that the 2+ cases are 2+. Is it possible that one of the pathologists is calling more cases as 2+ than the rest? I would have a lot of questions before modifying the staining protocol. It would be helpful you posted more info. Mark On Fri, Feb 1, 2013 at 6:52 PM, Wilson A wrote: > > Hi, > Our pathologists are concerned we may be reporting too many 2+ > HER2’s. Can someone help with this? > > Thanks, > Wilson > ___ > 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] HER-2
Which primary antibody and detection system are you using? Are you testing core biopsy tissue or excisional tumor? What criteria are your pathologists using to score a tumor "2+"? Richard Richard Cartun, MS, PhD Director, Histology & Immunopathology Director, Biospecimen Collections Programs Assistant Director, Anatomic Pathology Hartford Hospital/Clinical Laboratory Partners 80 Seymour Street Hartford, CT 06102 (860) 545-1596 (860) 545-2204 Fax >>> Wilson A 02/01/13 9:56 PM >>> Hi, Our pathologists are concerned we may be reporting too many 2+ HER2’s. Can someone help with this? Thanks, Wilson ___ 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] HER-2
That is a very strange question by your pathologists, since they are the ones doing the reporting. If they follow the reporting guidelines and arrive to a 2+ result, they should report it. Another question would be: are our lab's 2+ reports above the "mean" for other labs? The answer to this question can be done only if your find out the 2+ percentage for all labs is, and compare with yours. I think that your pathologists should contact CAP to find out if there are statistics on this issue. René J. From: Wilson A To: "histonet@lists.utsouthwestern.edu" Sent: Friday, February 1, 2013 9:52 PM Subject: [Histonet] HER-2 Hi, Our pathologists are concerned we may be reporting too many 2+ HER2’s. Can someone help with this? Thanks, Wilson ___ 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] Her-2 procedure
The protocol described by DAKO is very explicit, it produces consistent results and is the one I followed. Check it out. René J. From: Wilson A To: "histonet@lists.utsouthwestern.edu" Sent: Sunday, February 3, 2013 12:20 AM Subject: [Histonet] Her-2 procedure Hi, Please I will appreciate it, if you guys could share your HER-2 PROCEDURE with me. Thanks, Wilson ___ 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] Her-2 procedure
Hi, Please I will appreciate it, if you guys could share your HER-2 PROCEDURE with me. Thanks, Wilson ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] HER-2
Hi, Our pathologists are concerned we may be reporting too many 2+ HER2’s. Can someone help with this? Thanks, Wilson ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] her 2 neu, CISH vs FISH
Good afternoon histonetters We are currently investigating bringing Her 2 Neu CISH staining into our lab. FISH staining has too many logistics nightmares for me to consider, not to mention the cost of purchasing digital scanning equipment. Our pathologist are off site in 5 different hospitals. Does anyone know if there is a sensitivity issue between fluoresce and chromogen staining? Are oncologists receptive to having the Her 2 Neu confirmed by chromogenic ISH as opposed to fluoresce ISH? Anyone performing Her 2 Neu by CISH, what, if any, issues have you encountered. Any help and information would be appreciated. Thanks in advance. Cindy Cindy Pyse, CLT, HT (ASCP) Laboratory Manager X-Cell Laboratories 20 Northpointe Parkway Suite 100 Amherst, NY 14228 716-250-9235 etx. 232 e-mail cp...@x-celllab.com ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Her/2
marcia, was just getting ready to stain our her 2's , will let you know how they look. anita dudley providence hosp mobile, al > Date: Wed, 4 May 2011 12:54:29 -0400 > From: fu...@mercyhealth.com > To: histonet@lists.utsouthwestern.edu > Subject: [Histonet] Her/2 > > CAP validation Her/2 slides not staining as clear as before. Is anyone else > having any issues ? We use the Ventana system and our daily IHC slides are > staining > and controls are working well. Is there a coating on these slides from CAP ? > Thanks for any help ? > Marcia Funk HT,QIHC > > > > Marcia Funk > Histology Laboratory > Mercy Medical Center North Iowa > Mason City, IA, 50401 > 641-428-7907 > ___ > 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] Her/2
Yes, our slides look weak. I did slides for another hospital and they look weak as well. I have already contacted the CAP to see if they have received any other complaints. 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 >>> "Marcia Funk" 5/4/2011 12:54 PM >>> CAP validation Her/2 slides not staining as clear as before. Is anyone else having any issues ? We use the Ventana system and our daily IHC slides are staining and controls are working well. Is there a coating on these slides from CAP ? Thanks for any help ? Marcia Funk HT,QIHC Marcia Funk Histology Laboratory Mercy Medical Center North Iowa Mason City, IA, 50401 641-428-7907 ___ 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] Her/2
Hi Marcia, Our slides for the Her2 CAP survey stained just fine. We're using a Ventana XT to stain for Her2 by IHC. Mark On Wed, May 4, 2011 at 9:54 AM, Marcia Funk wrote: > CAP validation Her/2 slides not staining as clear as before. Is anyone > else having any issues ? We use the Ventana system and our daily IHC slides > are staining > and controls are working well. Is there a coating on these slides from CAP > ? > Thanks for any help ? > Marcia Funk HT,QIHC > > > > Marcia Funk > Histology Laboratory > Mercy Medical Center North Iowa > Mason City, IA, 50401 > 641-428-7907 > ___ > 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] Her/2
CAP validation Her/2 slides not staining as clear as before. Is anyone else having any issues ? We use the Ventana system and our daily IHC slides are staining and controls are working well. Is there a coating on these slides from CAP ? Thanks for any help ? Marcia Funk HT,QIHC Marcia Funk Histology Laboratory Mercy Medical Center North Iowa Mason City, IA, 50401 641-428-7907 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] HER 2
I-VIEW DAB Detection Kit from Ventena From: histonet-boun...@lists.utsouthwestern.edu [histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sara Baldwin/mhhcc.org [sbald...@mhhcc.org] Sent: Wednesday, September 22, 2010 3:32 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] HER 2 Which detection kit do you use? Thanks Pathology Supervisor Kathy Baldwin, SCT (ASCP) Memorial Hospital and Health Care Center sbald...@mhhcc.org Ph 812-482-0210, 482-0216, Fax 812-482-0232, Pager 812-481-0897 Confidential information, Authorized use only. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet - This electronic message may contain information that is confidential or legally privileged. It is intended only for the use of the individual(s) and entity named as recipients in the message. If you are not an intended recipient of this message, please notify the sender immediately and delete the material from any computer. Do not deliver, distribute, or copy this message, and do not disclose its contents or take any action in reliance on the information it contains. Thank you ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] HER 2
Which detection kit do you use? Thanks Pathology Supervisor Kathy Baldwin, SCT (ASCP) Memorial Hospital and Health Care Center sbald...@mhhcc.org Ph 812-482-0210, 482-0216, Fax 812-482-0232, Pager 812-481-0897 Confidential information, Authorized use only. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] her-2 neu validation
Hi Anita, We ran 25 amplified and 25 negative cases for our validation study. Good Luck. Debbie Nannenga, HTL(ASCP) QIHC InCyte Pathology Spokane, WA ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Her-2 Controls
Morning All, My chief pathologist has asked the following question. For all of those doing Her-2 Neu staining for scoring with the Vias system. How many control slides do you cut in advance and how long are they viable if kept refrigerated? Thanks in advance, Rae Ann Staskiewicz ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] her 2 validation
good morning!! just wanted to make sure about the number of slides that are required for validation for her 2. is it 25? thanks so much, anita dudley providence hospital mobile alabama _ Windows Live Hotmail gives you a free,exclusive gift. http://www.microsoft.com/windows/windowslive/hotmail_bl1/hotmail_bl1.aspx?ocid=PID23879::T:WLMTAGL:ON:WL:en-ww:WM_IMHM_7:092009___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet