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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Everyone, I have been preparing 0.1um Tetraspeck bead slides to use when measuring point spread functions on our Zeiss Elyra PS1 super resolution microscope and Zeiss LSM880 confocal with Airyscan. The problem is that over time the beads appear to swell to about 3 times in size and lose much of their fluorescence. I have tried many different mounting medias (hardening and nonhardening) all with the same result. Has anyone else experienced this problem? Any suggestions to solve the problem would be appreciated. Thanks, Jean -- Jean Ross Delaware Biotechnology Institute, BioImaging Center University of Delaware 15 Innovation Way Suite 117 Newark, DE 19711 Phone: (302)831-0620 Fax: (302)831-4841 |
Heddleston, John |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Jean, Over what time frame do you see them swell? In general we make bead slides relatively fresh (every ~2-3 weeks) to make sure the beads are good quality for PSF and alignment measurements. Cheers, John John M. Heddleston, PhD Applications Scientist Advanced Imaging Center at HHMI Janelia Ashburn, Virginia, USA E: [hidden email] Ph: (571) 209-4000, ext. 3356 -----Original Message----- From: Confocal Microscopy List <[hidden email]> On Behalf Of Jean Ross Sent: Friday, August 3, 2018 3:49 PM To: [hidden email] Subject: Tetraspeck beads for PSFs ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Everyone, I have been preparing 0.1um Tetraspeck bead slides to use when measuring point spread functions on our Zeiss Elyra PS1 super resolution microscope and Zeiss LSM880 confocal with Airyscan. The problem is that over time the beads appear to swell to about 3 times in size and lose much of their fluorescence. I have tried many different mounting medias (hardening and nonhardening) all with the same result. Has anyone else experienced this problem? Any suggestions to solve the problem would be appreciated. Thanks, Jean -- Jean Ross Delaware Biotechnology Institute, BioImaging Center University of Delaware 15 Innovation Way Suite 117 Newark, DE 19711 Phone: (302)831-0620 Fax: (302)831-4841 |
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