RE: [Histonet] Waste drum labeling
I would also be interested in the answers to this. 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 -Original Message- From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amber McKenzie Sent: Wednesday, November 28, 2012 1:16 AM Cc: histonet@lists.utsouthwestern.edu Subject: [Histonet] Waste drum labeling For EPA standards, how do you label your waste drums? I have one 55 lb drum that we only pour ventana waste in. What numbers do you write in the diamond to cover all the kits that you stain with? 2 reps from EPA came by my lab yesterday and said i needed an emergency phone list by our phone?? Does anyone have the checklist for EPA that small labs should follow? From: histonet-boun...@lists.utsouthwestern.edu [histonet-boun...@lists.utsouthwestern.edu] on behalf of Cristi Rigazio [cls71...@gmail.com] Sent: Tuesday, November 27, 2012 3:01 PM To: Rene J Buesa Cc: histonet@lists.utsouthwestern.edu; Elizabeth Cameron Subject: Re: [Histonet] Uneven Staining As most other bases have been covered, do you leave space between the slides in the rack? Once in a blue moon we had stains from the same rack that differed in intensity, after much troubleshooting we started putting space between the slides and we haven't had the problem since. Just an idea. Cristi Sent from my iPhone On Nov 27, 2012, at 12:24 PM, Rene J Buesa rjbu...@yahoo.com wrote: This is quite a puzzling situation. You have ruled out dewaxing (that was my first idea of cause) but I do not think that soaking will be the problem because the sections are fixed and infiltrated with paraffin, so there is no possibility of diluting in water. Thick/thin sections in a series is a very rare occurrence so I am also at a loss with this problem. Weak staining solutions could cause it but all sections in a series will be equally weak. Just in case, since you have covered the dewaxing, issue do the following: do not leave the sections too long in the water bath and dry them in the oven as soon as they are drained. René J. From: Elizabeth Cameron elizabeth.came...@jax.org To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu Sent: Tuesday, November 27, 2012 1:35 PM Subject: [Histonet] Uneven Staining About a year ago, I posted about issues with staining mouse kidney sections (see below for original post). We realized that part of the problem was the sections drying during staining, which has been resolved, but we are still having some issues with some slides staining well and others being very pale. This time it seems to be consistent across the slide, so I know it is not a drying issue. They are serial sections, so they are all cut together and stained together, and they are from the same animal. I don't believe deparaffinization is an issue - we have tried longer times with fresh solutions and it doesn't make a difference. We have also tried re-staining the slides after letting them sit in xylene overnight, and there is no difference in the staining. I am now thinking that it may be related to how long the sections soak or how long they sit on the waterbath. They are NBF fixed, and there is a fine line between soaking well for hydration and oversoaking, resulting in swelling. Has anyone experienced anything like this? Any other ideas? I am at a loss, and I'd really like for this to work! Thanks, Liz We are doing a Hale's colloidal iron stain (no counterstain) on serial sections of mouse kidneys. We are staining an entire kidney at a time (about 90-150 slides), and after many successful runs, we are now finding some slides in each batch with very uneven staining. Half of a section will stain as it should, and the rest of the section is very pale. It seems to be in a similar area from one section to the next, but not exactly the same area. It does not look like a deparaffinization issue. There may be two or three slides in a row like this, or just one section on a slide, followed by 30-40 that look fine. The sections are 6 microns. Any ideas on why this might be happening? Thanks! The information in this email, including attachments, may be confidential and is intended solely for the addressee(s). If you believe you received this email by mistake, please notify the sender by return email as soon as possible. ___ 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
Re: [Histonet] Waste drum labeling
With different products the toxicity level will vary. Write in the diamond the highest toxic level even if that is not the most abundant. By doing so you cover all inside the drum regarding their toxicity. I do not see the need for the emergency phone but if they told you to so so, do it. René J. From: Amber McKenzie amber.mcken...@gastrodocs.net To: Cc: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu Sent: Wednesday, November 28, 2012 1:16 AM Subject: [Histonet] Waste drum labeling For EPA standards, how do you label your waste drums? I have one 55 lb drum that we only pour ventana waste in. What numbers do you write in the diamond to cover all the kits that you stain with? 2 reps from EPA came by my lab yesterday and said i needed an emergency phone list by our phone?? Does anyone have the checklist for EPA that small labs should follow? From: histonet-boun...@lists.utsouthwestern.edu [histonet-boun...@lists.utsouthwestern.edu] on behalf of Cristi Rigazio [cls71...@gmail.com] Sent: Tuesday, November 27, 2012 3:01 PM To: Rene J Buesa Cc: histonet@lists.utsouthwestern.edu; Elizabeth Cameron Subject: Re: [Histonet] Uneven Staining As most other bases have been covered, do you leave space between the slides in the rack? Once in a blue moon we had stains from the same rack that differed in intensity, after much troubleshooting we started putting space between the slides and we haven't had the problem since. Just an idea. Cristi Sent from my iPhone On Nov 27, 2012, at 12:24 PM, Rene J Buesa rjbu...@yahoo.com wrote: This is quite a puzzling situation. You have ruled out dewaxing (that was my first idea of cause) but I do not think that soaking will be the problem because the sections are fixed and infiltrated with paraffin, so there is no possibility of diluting in water. Thick/thin sections in a series is a very rare occurrence so I am also at a loss with this problem. Weak staining solutions could cause it but all sections in a series will be equally weak. Just in case, since you have covered the dewaxing, issue do the following: do not leave the sections too long in the water bath and dry them in the oven as soon as they are drained. René J. From: Elizabeth Cameron elizabeth.came...@jax.org To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu Sent: Tuesday, November 27, 2012 1:35 PM Subject: [Histonet] Uneven Staining About a year ago, I posted about issues with staining mouse kidney sections (see below for original post). We realized that part of the problem was the sections drying during staining, which has been resolved, but we are still having some issues with some slides staining well and others being very pale. This time it seems to be consistent across the slide, so I know it is not a drying issue. They are serial sections, so they are all cut together and stained together, and they are from the same animal. I don't believe deparaffinization is an issue - we have tried longer times with fresh solutions and it doesn't make a difference. We have also tried re-staining the slides after letting them sit in xylene overnight, and there is no difference in the staining. I am now thinking that it may be related to how long the sections soak or how long they sit on the waterbath. They are NBF fixed, and there is a fine line between soaking well for hydration and oversoaking, resulting in swelling. Has anyone experienced anything like this? Any other ideas? I am at a loss, and I'd really like for this to work! Thanks, Liz We are doing a Hale's colloidal iron stain (no counterstain) on serial sections of mouse kidneys. We are staining an entire kidney at a time (about 90-150 slides), and after many successful runs, we are now finding some slides in each batch with very uneven staining. Half of a section will stain as it should, and the rest of the section is very pale. It seems to be in a similar area from one section to the next, but not exactly the same area. It does not look like a deparaffinization issue. There may be two or three slides in a row like this, or just one section on a slide, followed by 30-40 that look fine. The sections are 6 microns. Any ideas on why this might be happening? Thanks! The information in this email, including attachments, may be confidential and is intended solely for the addressee(s). If you believe you received this email by mistake, please notify the sender by return email as soon as possible. ___ 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 ___
