RE: [Histonet] Wax removal
We get our anti-fatigue mats from Lab Safety Supply. They have an extra thick one that I highly recommend. WANDA G. SMITH, HTL(ASCP)HT Pathology Supervisor TRIDENT MEDICAL CENTER 9330 Medical Plaza Drive Charleston, SC 29406 843-847-4586 843-847-4296 fax This email and any files transmitted with it may contain PRIVILEGED or CONFIDENTIAL information and may be read or used only by the intended recipient. If you are not the intended recipient of the email or any of its attachments, please be advised that you have received this email in error and that any use, dissemination, distribution, forwarding, printing, or copying of this email or any attached files is strictly prohibited. If you have received this email in error, please immediately purge it and all attachments and notify the sender by reply email or contact the sender at the number listed. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom Wells Sent: Thursday, July 15, 2010 4:48 PM To: Rathborne, Toni Cc: histonet@lists.utsouthwestern.edu; Hartz, Rhonda SktnHR Subject: RE: [Histonet] Wax removal Hi Rhonda, Where do you get the anti-fatigue mats Thanks. Tom Tom Wells BSc, ART Faculty School of Medical Laboratory Sciences British Columbia Institute of Technology Burnaby, BC Canada -histonet-boun...@lists.utsouthwestern.edu wrote: - To: Hartz, Rhonda SktnHR rhonda.ha...@saskatoonhealthregion.ca, histonet@lists.utsouthwestern.edu From: Rathborne, Toni trathbo...@somerset-healthcare.com Sent by: histonet-boun...@lists.utsouthwestern.edu Date: 07/15/2010 10:04AM Subject: RE: [Histonet] Wax removal We have a paraffin scraper that our Housekeeping staff uses. It was purchased from American MasterTech Scientific (item CPW04200E, and replacement blades item CPW04201P). We also have perforated anti-fatigue mats in aisles around the cutting stations which trap the wax and can be vacuumed/swept away when the mat is flipped. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Hartz, Rhonda SktnHR Sent: Thursday, July 15, 2010 12:42 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Wax removal Hi everyone; This may seem like a insignificant question, but we consistently have issues with injuries to our maintenance staff from cleaning the wax off of our floors. Housekeeping has laid sticky layered mats all over our floors (like large mouse traps), which they peel off layer by layer as they become wax covered. Apparently these are very expensive. Does anyone have any suggestions? Rhonda Hartz Technologist Supervisor Anatomic Pathology Division Saskatoon Health Region (306) 655-8197 rhonda.ha...@saskatoonhealthregion.ca ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet CONFIDENTIALITY NOTICE This message and any included attachments are from Somerset Medical Center and are intended only for the addressee. The information contained in this message is confidential and may contain privileged, confidential, proprietary and/or trade secret information entitled to protection and/or exemption from disclosure under applicable law. Unauthorized forwarding, printing, copying, distribution, or use of such information is strictly prohibited and may be unlawful. If you are not the addressee, please promptly delete this message and notify the sender of the delivery error by e-mail or you may call Somerset Medical Center's computer Help Desk at 908-685-2200, ext. 4050. Be sure to visit Somerset Medical Center's Web site - www.somersetmedicalcenter.com - for the most up-to-date news, event listings, health information and more. ___ 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] Hemoglobin Stain
Hi Linda, Thanks for the reply! No, I'm not limited to staining only. In fact, I will be performing some seperate IHC to demonstrate a couple of other proteins. It is simply my preference to use a histochemical technique for the following reasons. Firstly, from what I understand, staining will not be as laborious as IHC nor as difficult/technical to obtain positive results. Secondly, as this is part of my Honours year project, I would like to try my luck with several different techniques, and hemoglobin is the only molecule from the products I am looking at for which a simple histochemical approach is possible. Again, any suggestions would be highly valuable. Cheers, Anna Subject: RE: [Histonet] Hemoglobin Stain Date: Thu, 15 Jul 2010 11:41:54 -0500 From: lseb...@uwhealth.org To: annatay...@hotmail.com; histonet@lists.utsouthwestern.edu Anna, Are you limited to histochemical stains? Because if you're not, hemoglobin may be detected by immunohistochemistry quite nicely. Linda A. Sebree University of Wisconsin Hospital Clinics IHC/ISH Laboratory DB1-223 VAH 600 Highland Ave. Madison, WI 53792 (608)265-6596 -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Anna Taylor Sent: Thursday, July 15, 2010 11:37 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Hemoglobin Stain Hi all, In my quest for advice about what will be my very first attempt at histology, I have been recommended to post my query here. I'm attempting to demonstrate hemoglobin in FFPE lymph node sections. I've been able to find a couple of techniques (namely the Dunn Thompson technique and Okajima's technique), although I'm not sure how suitable either would be on lymph node sections? As I said, this will be my debut experience in histology/histochemistry so any advice/recommendations at all will be appreciated :)Thanks,Anna. _ View photos of singles in your area! Looking for a hot date? http://clk.atdmt.com/NMN/go/150855801/direct/01/ ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet _ If It Exists, You'll Find it on SEEK. Australia's #1 job site http://clk.atdmt.com/NMN/go/157639755/direct/01/___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Embedding multiple GI pieces on end in a paraffin block
Is there a way to do this without one or more pieces falling over? I saw in the archive the method for frozen sections-embed them on their sides in OCT, then cut on the end, but I don't think I'd be able to do that in paraffin. Would one of the tissue microarray methods work? (I've never done that before, so I have no idea.) Thanks in advance for all your help, Kathleen Principal Lab Technician Neurotoxicology Labs Molecular Pathology Facility Core Dept of Pharmacology Toxicology Rutgers, the State University of NJ 41 B Gordon Road Piscataway, NJ 08854 (732) 445-6914 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block
How many are we talking about? I embed 6 sections of mouse = bowel on end and it works? Just fill the mold, put it on the cold spo= t for a second, then on some room temperature area, the paraffin will harde= n slowly enough that you should be able to embed them? Sarah Goebel, B.A., = HT (ASCP) Histotechnician = /div XBiotech USA Inc. 8201 East Riverside Dr. Bldg 4 Suite 100 Austin, T= exas 78744 (512)386-5107 = br Original Message Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin block From: [1]kgrob...@rci.rutgers.ed= u Date: Fri, July 16, 2010 8:23 am To: histonet [2]h= isto...@lists.utsouthwestern.edu Is there a way to do this without one or more pieces falling over? I saw in the archive the method for frozen sections-embed them on their sides in= br OCT, then cut on the end, but I don't think I'd be able to do that in paraffin. Would one of the tissue microarray methods work? (I've never done that before, so I have no idea.) Thanks in advance for all your help, Kathleen Principal Lab Technician Neurotoxicology Labs Molecular Pathology Facility Core Dept of Pharmacology Toxicology Rutgers, the State University of NJ 41 B Gordon Road Piscataway, NJ 08854 (732) 445-6914 ___ Histonet mailing list [3]histo...@lists.utsou= thwestern.edu [4]http:= //lists.utsouthwestern.edu/mailman/listinfo/histonet References 1. 3Dmailto://kgrob...@rci.rutgers.edu/ 2. 3Dmailto://histonet@lists.utsouthwestern.edu/ 3. 3Dmailto://Histonet@lists.utsouthwestern.edu/ 4. 3Dhttp://lists.utsouthwestern.edu/mailman/listinfo/histonet; ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block
I have techs that embed 10-15 pieces on end in one block. Just cool the block slowly and move your pieces around quickly. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of kgrob...@rci.rutgers.edu Sent: Friday, July 16, 2010 10:24 AM To: histonet Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin block Is there a way to do this without one or more pieces falling over? I saw in the archive the method for frozen sections-embed them on their sides in OCT, then cut on the end, but I don't think I'd be able to do that in paraffin. Would one of the tissue microarray methods work? (I've never done that before, so I have no idea.) Thanks in advance for all your help, Kathleen Principal Lab Technician Neurotoxicology Labs Molecular Pathology Facility Core Dept of Pharmacology Toxicology Rutgers, the State University of NJ 41 B Gordon Road Piscataway, NJ 08854 (732) 445-6914 ___ 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 Block Storage
Hello histonetters, Does anyone know of a good source of used or economical plastic storage drawer cabinets for paraffin blocks? Auctions, used equipment, or otherwise retailers? Interested in purchasing some. We have thousands of blocks to store. Thanks! AB ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Embedding multiple GI pieces on end in a paraffin block
We regularly embed 6-12 pieces on end in one block without any special method. You just have to be quick... and don't leave the block on the cold plate very long... just touch the cold plate briefly while embedding the individual piece, then lift the block off the plate until you grab the next piece... repeat quickly and you'll run out of room in the mold before you'll have to worry about it hardening too much. Drew On Fri, Jul 16, 2010 at 11:23, kgrob...@rci.rutgers.edu wrote: Is there a way to do this without one or more pieces falling over? I saw in the archive the method for frozen sections-embed them on their sides in OCT, then cut on the end, but I don't think I'd be able to do that in paraffin. Would one of the tissue microarray methods work? (I've never done that before, so I have no idea.) Thanks in advance for all your help, Kathleen Principal Lab Technician Neurotoxicology Labs Molecular Pathology Facility Core Dept of Pharmacology Toxicology Rutgers, the State University of NJ 41 B Gordon Road Piscataway, NJ 08854 (732) 445-6914 ___ 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 Block Storage
In Vermont we are very frugal. What I have used for more years than I care to remember are pizza boxes from Pizza Hut. Our local Pizza Hut gives them to us for free. They are very sturdy and perfectly fit 11 rows across and approximately 36 blocks per row. I have 20 years of blocks stored this way. Lynne A. Bell, HT (ASCP) Technical Specialist, Histology Central Vermont Medical Center 130 Fisher Road Barre, VT 05641 802-371-4923 ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Lab in Aiken, South Carolina seeking histotech
Outpatient laboratory located in Aiken South Carolina is currently seeking a histotech. The company includes 20 specialty pathologists, more than 100 dedicated professionals, operates 9 patient service centers, and provides medical directorship for 18 hospitals throughout Georgia and northern Florida. Please contact me today for consideration Brian Feldman Principal Prometheus Healthcare Office 301-693-9057 Fax 301-368-2478 br...@prometheushealthcare.com mailto:br...@prometheushealthcare.com www.prometheushealthcare.com http://www.prometheushealthcare.com/ *** Stay up to date on the newest positions and healthcare trends nationwide on Twitter!*** http://twitter.com/PrometheusBlog ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block
To all, OK, looks like most of you are saying the same thing-work fast! :o) I've printed out all of your replies and discussed them with the graduate student who needs this done for her thesis, and she agrees with me-it's just going to take practice. I'll try the cool slowly/work fast suggestions first and see how that goes, then see about the trick with the cucumber (which sounds really cool!), slowly edging the mold onto the cold plate as I go, and using sponges to help flip the samples on end (and not necessarily in that order). I don't want to try too many things at once, lest I drive myself nuts. The first batch of samples should be coming sometime next week. Wish me luck, and thanks for all your help! Kathy ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] inking dyes
I use tattoo dyes. They work great and are much cheaper than tissue marking dyes. Cindy Pyse, CLT, HT (ASCP) Histology Supervisor X-Cell Laboratories e-mail cp...@x-celllab.com -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Diana McCaig Sent: Thursday, July 15, 2010 10:53 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] inking dyes Can someone provide me with a supplier of tissue marking dyes for use on the grossing bench. Diana McCaig Histology Lab Chatham Kent Health Alliance 80 Grand Avenue West Chatham. Ontario N7L 1B7 519-352-6401 (6604) This email communication and any files transmitted with it may contain confidential and or proprietary information and is provided for the use of the intended recipient only. Any review, retransmission or dissemination of this information by anyone other than the intended recipient is prohibited. If you receive this email in error, please contact the sender and delete this communication and any copies immediately. Thank you. ___ 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] Re: NG2 antibody/ Antigen retrieval/Protocol
I am trying to stain human glioma sections(as a positive control) using Anti-NG2 antibody. The tissue that I have is Paraffin embedded and I appreciate if somebody could send me the protocol for antigen retrieval ,antibody titer and IHC protocol. Let us know what Ab you are currently using ( Source and catalogue number) and also what detection/AR protocol you are using. Also, what problem do you have using your Ab? Best wishes, Carl ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
[Histonet] Cytology 100 slide limit
Our Cytology Supervisor was telling me about the 100 slide maximum that they can screen in a day. Our LIS is not capturing the NON-GYN slides being screened, so unless you are very diligent in recording the slides screened, you could go over the 100 limit. Our supervisor also believes the computer system should notify the user when the limit has been reached and prevent them from continuing. Is this a CAP requirement? How are you dealing with this problem or is it a problem for you? Victor -- Victor Tobias Clinical Applications Analyst University of Washington Medical Center Dept of Pathology Room BB220 1959 NE Pacific Seattle, WA 98195 vic...@pathology.washington.edu 206-598-2792 206-598-7659 Fax = Privileged, confidential or patient identifiable information may be contained in this message. This information is meant only for the use of the intended recipients. If you are not the intended recipient, or if the message has been addressed to you in error, do not read, disclose, reproduce, distribute, disseminate or otherwise use this transmission. Instead, please notify the sender by reply e-mail, and then destroy all copies of the message and any attachments. ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Re: [Histonet] Cytology 100 slide limit
Victor: As you wrote, either you have to be diligent in recording your work, or you will have to modify the software of the LIS system to account correctly. On the other hand, if you are dealing with liquid base samples usually using a Thin-Prep Imaging System (TIS) and the sample covers one-half or less of the slide surface, CLIA88 has expanded the limit from 100 to 200 slides/day. René J. --- On Fri, 7/16/10, Victor Tobias vic...@pathology.washington.edu wrote: From: Victor Tobias vic...@pathology.washington.edu Subject: [Histonet] Cytology 100 slide limit To: Histonet Histonet@lists.utsouthwestern.edu Date: Friday, July 16, 2010, 3:33 PM Our Cytology Supervisor was telling me about the 100 slide maximum that they can screen in a day. Our LIS is not capturing the NON-GYN slides being screened, so unless you are very diligent in recording the slides screened, you could go over the 100 limit. Our supervisor also believes the computer system should notify the user when the limit has been reached and prevent them from continuing. Is this a CAP requirement? How are you dealing with this problem or is it a problem for you? Victor -- Victor Tobias Clinical Applications Analyst University of Washington Medical Center Dept of Pathology Room BB220 1959 NE Pacific Seattle, WA 98195 vic...@pathology.washington.edu 206-598-2792 206-598-7659 Fax = Privileged, confidential or patient identifiable information may be contained in this message. This information is meant only for the use of the intended recipients. If you are not the intended recipient, or if the message has been addressed to you in error, do not read, disclose, reproduce, distribute, disseminate or otherwise use this transmission. Instead, please notify the sender by reply e-mail, and then destroy all copies of the message and any 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] New Job Opportunities
Hello everyone and happy Friday to all, Leica Microsystems is adding new positions and would like to hear from those of you who might be interested. The positions are for Field Support Specialists (FSS) and will be based in the following areas: Southeast Florida NYC/Bronx/NJ MD/VA/DC TN/MS/AR NM/TX/western OK CO/WY/MT Southern IL/Iowa Some of the responsibilities include in-field support for IHC, conducting demonstrations and post-sales customer training, performing validations and optimization, and providing technical support for remote problem solving. If you are interested in trying something different and feel that you are qualified, please contact Linda Jordan, HR Recruiter at hrco...@leica-microsystems.com. Kind regards, Jan Minshew Marketing Manager Leica Microsystems Biosystems Division 2345 Waukegan Road Bannockburn, IL 60015 Office: 847.405.7051 Cell: 847.970.8468 Fax: 847.405.6560 www.leica-microsystems.com Click Here for this month's special offers! http://www.leica-microsystems.com/bsdspecial __ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email __ ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Cytology 100 slide limit
Victor, Rene is correct in stating that CLIA allows Gyn Liquid Based Paps to be counted as 1/2 slide. It gets tricky when you start mixing 1/2 slide counts and full slide counts in making sure the techs do not exceed 100 slides (or in the case of LBP's 200 slides). If you get a lot of FNA's the counts can go up very quickly. Most LIS systems can prevent Techs from exceeding their limit. I would check again to see why your LIS is not capturing the NON-Gyn slides. Another CAP and CLIA requirement is that each 6 months, the cytotechs are supposed to have a Competency Assessment where the Medical Director signs off on the maximum number of slides each tech is qualified to screen. This is the number that most labs place in the LIS as the max that particular tech can review. What LIS system do you have? Steve -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa Sent: Friday, July 16, 2010 5:21 PM To: Histonet; Victor Tobias Subject: Re: [Histonet] Cytology 100 slide limit Victor: As you wrote, either you have to be diligent in recording your work, or you will have to modify the software of the LIS system to account correctly. On the other hand, if you are dealing with liquid base samples usually using a Thin-Prep Imaging System (TIS) and the sample covers one-half or less of the slide surface, CLIA88 has expanded the limit from 100 to 200 slides/day. René J. --- On Fri, 7/16/10, Victor Tobias vic...@pathology.washington.edu wrote: From: Victor Tobias vic...@pathology.washington.edu Subject: [Histonet] Cytology 100 slide limit To: Histonet Histonet@lists.utsouthwestern.edu Date: Friday, July 16, 2010, 3:33 PM Our Cytology Supervisor was telling me about the 100 slide maximum that they can screen in a day. Our LIS is not capturing the NON-GYN slides being screened, so unless you are very diligent in recording the slides screened, you could go over the 100 limit. Our supervisor also believes the computer system should notify the user when the limit has been reached and prevent them from continuing. Is this a CAP requirement? How are you dealing with this problem or is it a problem for you? Victor -- Victor Tobias Clinical Applications Analyst University of Washington Medical Center Dept of Pathology Room BB220 1959 NE Pacific Seattle, WA 98195 vic...@pathology.washington.edu 206-598-2792 206-598-7659 Fax = Privileged, confidential or patient identifiable information may be contained in this message. This information is meant only for the use of the intended recipients. If you are not the intended recipient, or if the message has been addressed to you in error, do not read, disclose, reproduce, distribute, disseminate or otherwise use this transmission. Instead, please notify the sender by reply e-mail, and then destroy all copies of the message and any 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] Embedding multiple GI pieces on end in a paraffin block
Hello, The way I used to embed GI specimens is to place them on end on a stack of specimen bags that have solidified, since they are already in place, then you can pick them up quickly. I did this with sectioned arterial artieries or vas deferens this worked like a dream. Robyn Vazquez Date: Fri, 16 Jul 2010 11:00:01 -0500 From: mpe...@grhs.net To: kgrob...@rci.rutgers.edu; histonet@lists.utsouthwestern.edu Subject: RE: [Histonet] Embedding multiple GI pieces on end in a paraffin block CC: I have techs that embed 10-15 pieces on end in one block. Just cool the block slowly and move your pieces around quickly. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of kgrob...@rci.rutgers.edu Sent: Friday, July 16, 2010 10:24 AM To: histonet Subject: [Histonet] Embedding multiple GI pieces on end in a paraffin block Is there a way to do this without one or more pieces falling over? I saw in the archive the method for frozen sections-embed them on their sides in OCT, then cut on the end, but I don't think I'd be able to do that in paraffin. Would one of the tissue microarray methods work? (I've never done that before, so I have no idea.) Thanks in advance for all your help, Kathleen Principal Lab Technician Neurotoxicology Labs Molecular Pathology Facility Core Dept of Pharmacology Toxicology Rutgers, the State University of NJ 41 B Gordon Road Piscataway, NJ 08854 (732) 445-6914 ___ 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
[Histonet] Wax removal
Hi, You can get abrasive pads that have adhesive on one side. They are usually used on stairs. They are like 8 inch wide 3 foot long strips of sandpaper that stick (really well) to the floor. I have them placed about 1 per foot along main traffic areas. I don't recall off the top of my head where we got them from, but if you'd like, I'll look it up on Monday. Amos Message: 6 Date: Thu, 15 Jul 2010 10:42:26 -0600 From: Hartz, Rhonda SktnHR rhonda.ha...@saskatoonhealthregion.ca Subject: [Histonet] Wax removal To: histonet@lists.utsouthwestern.edu Message-ID: b7f15445a710ba4fa7b48f2c55134ad404b3d...@lou.sktnhr.ca Content-Type: text/plain; charset=US-ASCII Hi everyone; This may seem like a insignificant question, but we consistently have issues with injuries to our maintenance staff from cleaning the wax off of our floors. Housekeeping has laid sticky layered mats all over our floors (like large mouse traps), which they peel off layer by layer as they become wax covered. Apparently these are very expensive. Does anyone have any suggestions? Rhonda Hartz Technologist Supervisor Anatomic Pathology Division Saskatoon Health Region (306) 655-8197 rhonda.ha...@saskatoonhealthregion.ca ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
RE: [Histonet] Wax removal
We get our anti-fatigue mats from Sam's make sure you get the red ones and not the black ones. They are in the office materials area. Connie G. From: wanda.sm...@hcahealthcare.com To: tom_we...@bcit.ca; trathbo...@somerset-healthcare.com Date: Fri, 16 Jul 2010 09:00:01 -0500 Subject: RE: [Histonet] Wax removal CC: histonet@lists.utsouthwestern.edu; rhonda.ha...@saskatoonhealthregion.ca We get our anti-fatigue mats from Lab Safety Supply. They have an extra thick one that I highly recommend. WANDA G. SMITH, HTL(ASCP)HT Pathology Supervisor TRIDENT MEDICAL CENTER 9330 Medical Plaza Drive Charleston, SC 29406 843-847-4586 843-847-4296 fax This email and any files transmitted with it may contain PRIVILEGED or CONFIDENTIAL information and may be read or used only by the intended recipient. If you are not the intended recipient of the email or any of its attachments, please be advised that you have received this email in error and that any use, dissemination, distribution, forwarding, printing, or copying of this email or any attached files is strictly prohibited. If you have received this email in error, please immediately purge it and all attachments and notify the sender by reply email or contact the sender at the number listed. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom Wells Sent: Thursday, July 15, 2010 4:48 PM To: Rathborne, Toni Cc: histonet@lists.utsouthwestern.edu; Hartz, Rhonda SktnHR Subject: RE: [Histonet] Wax removal Hi Rhonda, Where do you get the anti-fatigue mats Thanks. Tom Tom Wells BSc, ART Faculty School of Medical Laboratory Sciences British Columbia Institute of Technology Burnaby, BC Canada -histonet-boun...@lists.utsouthwestern.edu wrote: - To: Hartz, Rhonda SktnHR rhonda.ha...@saskatoonhealthregion.ca, histonet@lists.utsouthwestern.edu From: Rathborne, Toni trathbo...@somerset-healthcare.com Sent by: histonet-boun...@lists.utsouthwestern.edu Date: 07/15/2010 10:04AM Subject: RE: [Histonet] Wax removal We have a paraffin scraper that our Housekeeping staff uses. It was purchased from American MasterTech Scientific (item CPW04200E, and replacement blades item CPW04201P). We also have perforated anti-fatigue mats in aisles around the cutting stations which trap the wax and can be vacuumed/swept away when the mat is flipped. -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of Hartz, Rhonda SktnHR Sent: Thursday, July 15, 2010 12:42 PM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] Wax removal Hi everyone; This may seem like a insignificant question, but we consistently have issues with injuries to our maintenance staff from cleaning the wax off of our floors. Housekeeping has laid sticky layered mats all over our floors (like large mouse traps), which they peel off layer by layer as they become wax covered. Apparently these are very expensive. Does anyone have any suggestions? Rhonda Hartz Technologist Supervisor Anatomic Pathology Division Saskatoon Health Region (306) 655-8197 rhonda.ha...@saskatoonhealthregion.ca ___ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet CONFIDENTIALITY NOTICE This message and any included attachments are from Somerset Medical Center and are intended only for the addressee. The information contained in this message is confidential and may contain privileged, confidential, proprietary and/or trade secret information entitled to protection and/or exemption from disclosure under applicable law. Unauthorized forwarding, printing, copying, distribution, or use of such information is strictly prohibited and may be unlawful. If you are not the addressee, please promptly delete this message and notify the sender of the delivery error by e-mail or you may call Somerset Medical Center's computer Help Desk at 908-685-2200, ext. 4050. Be sure to visit Somerset Medical Center's Web site - www.somersetmedicalcenter.com - for the most up-to-date news, event listings, health information and more. ___ 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