Earl_Sanford |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I have a user that insists on growing their cells in plastic well plates and am trying to come up with a good way to punch or cut out individual wells without disturbing the cells too much. My thought is that if I can cut the wells out I can flip them over in a glass bottom petri dish or examine them straight down in a petri dish with water dippers. If anyone knows of a tool that work well to do this I would greatly appreciate hearing about it - particularly if it performs well in 96 and 384 well plates. Any tips on convincing researchers to switch over to glass bottom plates would also be appreciated. We have tried showing them the difference in image quality between samples grown on glass versus plastic but can not seem to get them to switch. Thanks, Earl Sanford |
Oshel, Philip Eugene |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I used to do this using a core borer. Find the size borer just big enough to fit the well, and gently heat it. The hot borer will cut the well bottom free around the edges. Use a forceps or something on one edge and poke that edge up into the bore, rotating the plastic disc. Grab the edge that rotates down, and remove it from the borer. But be quick. I did this on 96 well plates, 384 well plates may not work. Phil You're at Corning, and they don't like glass? >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >I have a user that insists on growing their cells in plastic well >plates and am >trying to come up with a good way to punch or cut out individual wells without >disturbing the cells too much. My thought is that if I can cut the wells out I >can flip them over in a glass bottom petri dish or examine them straight down >in a petri dish with water dippers. > >If anyone knows of a tool that work well to do this I would greatly appreciate >hearing about it - particularly if it performs well in 96 and 384 >well plates. Any >tips on convincing researchers to switch over to glass bottom plates would >also be appreciated. We have tried showing them the difference in image >quality between samples grown on glass versus plastic but can not seem to >get them to switch. > >Thanks, >Earl Sanford -- Philip Oshel Microscopy Facility Supervisor Biology Department 024C Brooks Hall Central Michigan University Mt. Pleasant, MI 48859 (989) 774-3576 |
Ignatius, Mike-2 |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Long ago I used a hot wire stretched tight to cut the bottoms off of plastic 96 well round bottomed wells- caught them in a an arrayed rack of tubes underneath. 96 wells in 10 seconds. Do it in a fume hood though. The strongest case against plastic bottoms is the long working distance and thus low NA objectives that have to used. Loss of resolution and signal. Mike Ignatius -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Philip Oshel Sent: Tuesday, March 01, 2011 1:04 PM To: [hidden email] Subject: Re: Is there an easy way to punch out plastic well plates ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I used to do this using a core borer. Find the size borer just big enough to fit the well, and gently heat it. The hot borer will cut the well bottom free around the edges. Use a forceps or something on one edge and poke that edge up into the bore, rotating the plastic disc. Grab the edge that rotates down, and remove it from the borer. But be quick. I did this on 96 well plates, 384 well plates may not work. Phil You're at Corning, and they don't like glass? >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >I have a user that insists on growing their cells in plastic well >plates and am >trying to come up with a good way to punch or cut out individual wells without >disturbing the cells too much. My thought is that if I can cut the wells out I >can flip them over in a glass bottom petri dish or examine them straight down >in a petri dish with water dippers. > >If anyone knows of a tool that work well to do this I would greatly appreciate >hearing about it - particularly if it performs well in 96 and 384 >well plates. Any >tips on convincing researchers to switch over to glass bottom plates would >also be appreciated. We have tried showing them the difference in image >quality between samples grown on glass versus plastic but can not seem to >get them to switch. > >Thanks, >Earl Sanford -- Philip Oshel Microscopy Facility Supervisor Biology Department 024C Brooks Hall Central Michigan University Mt. Pleasant, MI 48859 (989) 774-3576 |
Moninger, Thomas |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I've found that disposable surgical cauterizers also work well. Tom -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Ignatius, Mike Sent: Tuesday, March 01, 2011 3:14 PM To: [hidden email] Subject: Re: Is there an easy way to punch out plastic well plates ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Long ago I used a hot wire stretched tight to cut the bottoms off of plastic 96 well round bottomed wells- caught them in a an arrayed rack of tubes underneath. 96 wells in 10 seconds. Do it in a fume hood though. The strongest case against plastic bottoms is the long working distance and thus low NA objectives that have to used. Loss of resolution and signal. Mike Ignatius -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Philip Oshel Sent: Tuesday, March 01, 2011 1:04 PM To: [hidden email] Subject: Re: Is there an easy way to punch out plastic well plates ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I used to do this using a core borer. Find the size borer just big enough to fit the well, and gently heat it. The hot borer will cut the well bottom free around the edges. Use a forceps or something on one edge and poke that edge up into the bore, rotating the plastic disc. Grab the edge that rotates down, and remove it from the borer. But be quick. I did this on 96 well plates, 384 well plates may not work. Phil You're at Corning, and they don't like glass? >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >I have a user that insists on growing their cells in plastic well >plates and am >trying to come up with a good way to punch or cut out individual wells without >disturbing the cells too much. My thought is that if I can cut the wells out I >can flip them over in a glass bottom petri dish or examine them straight down >in a petri dish with water dippers. > >If anyone knows of a tool that work well to do this I would greatly appreciate >hearing about it - particularly if it performs well in 96 and 384 >well plates. Any >tips on convincing researchers to switch over to glass bottom plates would >also be appreciated. We have tried showing them the difference in image >quality between samples grown on glass versus plastic but can not seem to >get them to switch. > >Thanks, >Earl Sanford -- Philip Oshel Microscopy Facility Supervisor Biology Department 024C Brooks Hall Central Michigan University Mt. Pleasant, MI 48859 (989) 774-3576 ________________________________ Notice: This UI Health Care e-mail (including attachments) is covered by the Electronic Communications Privacy Act, 18 U.S.C. 2510-2521, is confidential and may be legally privileged. If you are not the intended recipient, you are hereby notified that any retention, dissemination, distribution, or copying of this communication is strictly prohibited. Please reply to the sender that you have received the message in error, then delete it. Thank you. ________________________________ |
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