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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. ***** We have been trying to do FRAP experiments on the Zeiss 880, but we are having difficulties getting accurate times. Typically, we take 2 to 4 before images, then a bleach, and then the recovery sequence. The problem is that we do not know how to get accurate times for the sequence after the bleaching. I used to do this on a Leica SP2 and the times were well reported in the metadata, but I cannot find the times in the Zeiss files. Any help would be appreciated. Thank you. Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY 10016 [hidden email]<mailto:[hidden email]> http://nyulmc.org/micros http://microscopynotes.com/ Voice direct only, no text or messages: 1-914-309-3270 and 1-646-501-0567 |
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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. ***** Did you tried to look at the table in Mean ROI tab? I'm pretty sure you can get it there. Uzi Uzi Hadad, PhD Shared Resource Laboratory for Flow Cytometry & Bio-Imaging Ilse Katz Institute for Nanoscale Science and Technology Ben-Gurion University of the Negev Beer Sheva 84105, Israel Office: +972-8-6428674 | Blgd 51, Room 325 Lab: +972-8-6428648 | Room 326 On Wed, Aug 19, 2020, 23:44 Cammer, Michael < [hidden email]> wrote: > ***** > 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. > ***** > > We have been trying to do FRAP experiments on the Zeiss 880, but we are > having difficulties getting accurate times. > > > Typically, we take 2 to 4 before images, then a bleach, and then the > recovery sequence. > > > The problem is that we do not know how to get accurate times for the > sequence after the bleaching. I used to do this on a Leica SP2 and the > times were well reported in the metadata, but I cannot find the times in > the Zeiss files. Any help would be appreciated. > > > Thank you. > > > Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory > > NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY > 10016 > > [hidden email]<mailto:[hidden email]> > http://nyulmc.org/micros http://microscopynotes.com/ > > Voice direct only, no text or messages: 1-914-309-3270 and 1-646-501-0567 > |
Rebecca M. Williams |
In reply to this post by Cammer, Michael-2
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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 Michael -- As I recall this info is remarkably difficult to get. The only way I could get it was to have zen display a timepoint on the images. You do this using the graphics tab under the display. Make sure you have "show all" checked (hidden to the right). Choose the More. . . option and then coordinate -> time. Becky Rebecca Williams Director, BRC Imaging Facility B35 Weill Hall Cornell University (607) 255-4610 -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Cammer, Michael Sent: Wednesday, August 19, 2020 4:44 PM To: [hidden email] Subject: Zeiss 880 timing question ***** 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. ***** We have been trying to do FRAP experiments on the Zeiss 880, but we are having difficulties getting accurate times. Typically, we take 2 to 4 before images, then a bleach, and then the recovery sequence. The problem is that we do not know how to get accurate times for the sequence after the bleaching. I used to do this on a Leica SP2 and the times were well reported in the metadata, but I cannot find the times in the Zeiss files. Any help would be appreciated. Thank you. Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY 10016 [hidden email]<mailto:[hidden email]> http://nyulmc.org/micros http://microscopynotes.com/ Voice direct only, no text or messages: 1-914-309-3270 and 1-646-501-0567 |
Toth, Peter Tibor |
In reply to this post by Cammer, Michael-2
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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 Michael, You can drop the Zeiss .czi file into Fiji. In the Metadata viewing column check the "Display OME-XML metadata" checkbox. Metadata with times, etc. opens up in a separate window. -Peter -- Peter T. Toth, PhD Director, Fluorescence Imaging Core The University of Illinois at Chicago 835 S. Wolcott Ave (MSB), E-325 Phone: (312) 996-0003 [hidden email] ________________________________ From: Confocal Microscopy List <[hidden email]> on behalf of Cammer, Michael <[hidden email]> Sent: Wednesday, August 19, 2020 3:43 PM To: [hidden email] <[hidden email]> Subject: Zeiss 880 timing question ***** 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. ***** We have been trying to do FRAP experiments on the Zeiss 880, but we are having difficulties getting accurate times. Typically, we take 2 to 4 before images, then a bleach, and then the recovery sequence. The problem is that we do not know how to get accurate times for the sequence after the bleaching. I used to do this on a Leica SP2 and the times were well reported in the metadata, but I cannot find the times in the Zeiss files. Any help would be appreciated. Thank you. Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY 10016 [hidden email]<mailto:[hidden email]> http://nyulmc.org/micros http://microscopynotes.com/ Voice direct only, no text or messages: 1-914-309-3270 and 1-646-501-0567 |
Cammer, Michael-2 |
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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. ***** I want to thank the many replies to my question including from Zeiss directly. I had been struggling with the regular metadata and didn't even think to look at the XML version separately. This may also answer a question someone asked about FRAP a few weeks ago. In addition to the Elyra images, I opened a FRAP sequence from the Zeiss 880 and while not all the information to reconstruct the settings is displayed, this combined with the ROIs may be sufficient to run the analyses. Best regards- Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY 10016 Office: 646-501-0567 Cell: 914-309-3270 [hidden email] http://nyulmc.org/micros http://microscopynotes.com/ -----Original Message----- From: Confocal Microscopy List <[hidden email]> On Behalf Of Toth, Peter Tibor Sent: Thursday, August 20, 2020 12:35 PM To: [hidden email] Subject: Re: Zeiss 880 timing question [EXTERNAL] ***** To join, leave or search the confocal microscopy listserv, go to: https://urldefense.proofpoint.com/v2/url?u=http-3A__lists.umn.edu_cgi-2Dbin_wa-3FA0-3Dconfocalmicroscopy&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=RO7Yq9eP8ZfxCNopWy3q-eVrSLkPaNAAwRVC50ldYZ8&e= Post images on https://urldefense.proofpoint.com/v2/url?u=http-3A__www.imgur.com&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=gaLQ5Cex9nn2TfrvgDixI_WcxdQAfj014E36KO4K1Dw&e= and include the link in your posting. ***** Hi Michael, You can drop the Zeiss .czi file into Fiji. In the Metadata viewing column check the "Display OME-XML metadata" checkbox. Metadata with times, etc. opens up in a separate window. -Peter -- Peter T. Toth, PhD Director, Fluorescence Imaging Core The University of Illinois at Chicago 835 S. Wolcott Ave (MSB), E-325 Phone: (312) 996-0003 [hidden email] ________________________________ From: Confocal Microscopy List <[hidden email]> on behalf of Cammer, Michael <[hidden email]> Sent: Wednesday, August 19, 2020 3:43 PM To: [hidden email] <[hidden email]> Subject: Zeiss 880 timing question ***** To join, leave or search the confocal microscopy listserv, go to: https://urldefense.proofpoint.com/v2/url?u=http-3A__lists.umn.edu_cgi-2Dbin_wa-3FA0-3Dconfocalmicroscopy&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=RO7Yq9eP8ZfxCNopWy3q-eVrSLkPaNAAwRVC50ldYZ8&e= Post images on https://urldefense.proofpoint.com/v2/url?u=http-3A__www.imgur.com&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=gaLQ5Cex9nn2TfrvgDixI_WcxdQAfj014E36KO4K1Dw&e= and include the link in your posting. ***** We have been trying to do FRAP experiments on the Zeiss 880, but we are having difficulties getting accurate times. Typically, we take 2 to 4 before images, then a bleach, and then the recovery sequence. The problem is that we do not know how to get accurate times for the sequence after the bleaching. I used to do this on a Leica SP2 and the times were well reported in the metadata, but I cannot find the times in the Zeiss files. Any help would be appreciated. Thank you. Michael Cammer, Sr Research Scientist, DART Microscopy Laboratory NYU Langone Health, 540 First Avenue, SK2 Microscopy Suite, New York, NY 10016 [hidden email]<mailto:[hidden email]> https://urldefense.proofpoint.com/v2/url?u=http-3A__nyulmc.org_micros&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=W0S_dPKuif2Wetayp0kp72GnoskC0c3LU0XZ2iQEv6E&e= https://urldefense.proofpoint.com/v2/url?u=http-3A__microscopynotes.com_&d=DwIFAg&c=j5oPpO0eBH1iio48DtsedeElZfc04rx3ExJHeIIZuCs&r=E0xNnPAQpUbDiPlC50tp7rW2nBkvV7fujQf0RknE5bU&m=vzTvuCdTuXlNt7xwl2BxjS4F_j4AB9ovE0B2SIQGqeE&s=PRasAxaBALJ_xYlaShcnTFrKD0jWSHcR0BFQ3XACnu8&e= Voice direct only, no text or messages: 1-914-309-3270 and 1-646-501-0567 |
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