*****
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. ***** Dear colleagues, have any of you tried the AiryScan (Zeiss) system together with a multiphoton platform? If yes, do you think is it possible to achieve true "SHG super resolution"? Thanks in advance for your comments/opinion. Best, Mar |
Periasamy, Ammasi (ap3t)-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. ***** Yes, we collected 2photon Airyscan images in the fly brain and mouse embryo, the S/N is 2-3 times better than the conventional 2photon. The lateral resolution is also improved about 1.5 times in the fly brain at about 100 micron depth compared to confocal. I would expect you should get better lateral resolution for SHG and THG imaging. Hope this helps. Ammasi Dr. Ammasi Periasamy Professor & Center Director, WM Keck Center for Cellular Imaging, Department of Biology, Univeristy of Virginia, 90 Geldard Dr., Charlottesville, VA 22904, USA. http://www.kcci.virginia.edu/people/profile/ap3t Phone: (434) 243-7602 or 982-4869 Fax: (434) 982-5210 E-mail: [hidden email] FRET/FLIM Workshop-March 11-15, 2019: http://www.kcci.virginia.edu/workshop -----Original Message----- From: Confocal Microscopy List <[hidden email]> On Behalf Of Mar Baha Sent: Monday, May 21, 2018 7:05 PM To: [hidden email] Subject: AiryScan vs. "superresolution" SHG? ***** 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. ***** Dear colleagues, have any of you tried the AiryScan (Zeiss) system together with a multiphoton platform? If yes, do you think is it possible to achieve true "SHG super resolution"? Thanks in advance for your comments/opinion. Best, Mar |
Roland Nitschke |
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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 presented a talk at the FOM 2018: http://www.focusonmicroscopy.org/2018/PDF/1096_Kleppe.pdf, that showed strong improvement in image resolution and noise by using airy scan detection for 2P fluorescence imaging down to a depth of 800 µm. We did not use thicker samples for our tests. I expect it should be the same for SHG imaging. Best regards Roland Nitschke *********************************************************** *********************************************************** Dr. Roland Nitschke Albert-Ludwigs University Freiburg Life Imaging Center (LIC) in ZBSA Microscopy and Image Analysis Platform (MIAP) Habsburgerstr.49 79104 Freiburg Germany e-mail: [hidden email] <mailto:[hidden email]> phone: +49 761 203 2934 fax: +49 761 203 2941 web LIC: https://miap.eu/miap-units/life-imaging-center-lic/ web MIAP: https://miap.eu <https://miap.eu/> Am 22.05.2018 um 01:30 schrieb Periasamy, Ammasi (ap3t): > ***** > 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. > ***** > > Yes, we collected 2photon Airyscan images in the fly brain and mouse embryo, the S/N is 2-3 times better than the conventional 2photon. The lateral resolution is also improved about 1.5 times in the fly brain at about 100 micron depth compared to confocal. > I would expect you should get better lateral resolution for SHG and THG imaging. > Hope this helps. > Ammasi > > Dr. Ammasi Periasamy > Professor & Center Director, > WM Keck Center for Cellular Imaging, > Department of Biology, Univeristy of Virginia, > 90 Geldard Dr., Charlottesville, VA 22904, USA. > > http://www.kcci.virginia.edu/people/profile/ap3t > Phone: (434) 243-7602 or 982-4869 > Fax: (434) 982-5210 > E-mail: [hidden email] > > FRET/FLIM Workshop-March 11-15, 2019: http://www.kcci.virginia.edu/workshop > > -----Original Message----- > From: Confocal Microscopy List <[hidden email]> On Behalf Of Mar Baha > Sent: Monday, May 21, 2018 7:05 PM > To: [hidden email] > Subject: AiryScan vs. "superresolution" SHG? > > ***** > 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. > ***** > > Dear colleagues, > > have any of you tried the AiryScan (Zeiss) system together with a multiphoton platform? > If yes, do you think is it possible to achieve true "SHG super resolution"? > > Thanks in advance for your comments/opinion. > Best, > Mar |
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