Gary Laevsky |
*****
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 All, We been working on this for a few months, and not getting what we need. The goal is to image the whole critter on one of our light-sheets. We've tried CUBIC, and iDisco (using DCM and Ethyl Cinnamate). Any ideas? Thanks so much. -- Best, Gary Laevsky, Ph.D. Director, Confocal Imaging Facility Nikon Center of Excellence Co-Founder, North Atlantic Microscopy Society (NAMS) https://namsmicroscopy.com/ Dept. of Molecular Biology Washington Rd. Princeton University Princeton, New Jersey, 08544-1014 (O) 609 258 5432 (C) 508 507 1310 North Atlantic Microscopy Society Spring Meeting at UPENN, April 23, 2020. |
Arvydas Matiukas |
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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 Gary, How big is your critter (sorry just noticed the name in the subject but no dimensions provided)and what type of tissues/cells does it contain? I was able to clear heart=muscle tissue up to 10mm thick using the old good BABB (though not compatible with many dyes and FP). The modern clearing methods are good for brain but not working on the heart because of significantly higher refractive index. Best, Arvydas +++++++++++++++++++++++++++++ Arvydas Matiukas, Ph.D. Manager of NRB Shared Research Equipment Director of Confocal&Two-Photon Core SUNY Upstate Medical University >>> Gary Laevsky <[hidden email]> 02/10/20 8:10 AM >>> ***** 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=DwIBaQ&c=ogn2iPkgF7TkVSicOVBfKg&r=DtXPX1Vw9uh8rqlCEC9BTBr2oYBP4dEG1ecsgK6l-4k&m=dYD-JqP3bCJyPD3yje4UrA1paF0oSWgb9nsZ5N4MKWA&s=auSPMRnt4qGosfU9Edr1RRjpKtgU21cImpwKknvfpEQ&e= Post images on https://urldefense.proofpoint.com/v2/url?u=http-3A__www.imgur.com&d=DwIBaQ&c=ogn2iPkgF7TkVSicOVBfKg&r=DtXPX1Vw9uh8rqlCEC9BTBr2oYBP4dEG1ecsgK6l-4k&m=dYD-JqP3bCJyPD3yje4UrA1paF0oSWgb9nsZ5N4MKWA&s=XBlBbGP754VIN-RYLZUWiG22hm4XHiT6f48k7-fikIE&e= and include the link in your posting. ***** Hi All, We been working on this for a few months, and not getting what we need. The goal is to image the whole critter on one of our light-sheets. We've tried CUBIC, and iDisco (using DCM and Ethyl Cinnamate). Any ideas? Thanks so much. -- Best, Gary Laevsky, Ph.D. Director, Confocal Imaging Facility Nikon Center of Excellence Co-Founder, North Atlantic Microscopy Society (NAMS) https://urldefense.proofpoint.com/v2/url?u=https-3A__namsmicroscopy.com_&d=DwIBaQ&c=ogn2iPkgF7TkVSicOVBfKg&r=DtXPX1Vw9uh8rqlCEC9BTBr2oYBP4dEG1ecsgK6l-4k&m=dYD-JqP3bCJyPD3yje4UrA1paF0oSWgb9nsZ5N4MKWA&s=KtC4lMFaev7ApILM9jF34BqK3BiwijmfniRe3ZXMEKA&e= Dept. of Molecular Biology Washington Rd. Princeton University Princeton, New Jersey, 08544-1014 (O) 609 258 5432 (C) 508 507 1310 North Atlantic Microscopy Society Spring Meeting at UPENN, April 23, 2020. |
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