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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. ***** Dear all, I'm keen to find out what your favoured pair of fluorescent proteins for multiphoton microcopy, in which you’re limited to a single excitation wavelength (to avoid compromising too much with each). And which excitation wavelengths you use with them. Thanks in advance, Graham — Graham Wright, PhD Director, A*STAR Microscopy Platform T: +65 6407 0167 E: [hidden email] W: www.a-star.edu.sg/imb/Tech-Platforms/AMP-Light-Microscopy |
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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. ***** BFP/GFP and BFP/YFP worked well with 800-820 nm excitation in Zebrafish. Good luck! Ekaterina -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Graham Wright Sent: Tuesday, October 16, 2018 3:38 PM To: [hidden email] Subject: FPs for MP ***** 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 all, I'm keen to find out what your favoured pair of fluorescent proteins for multiphoton microcopy, in which you’re limited to a single excitation wavelength (to avoid compromising too much with each). And which excitation wavelengths you use with them. Thanks in advance, Graham — Graham Wright, PhD Director, A*STAR Microscopy Platform T: +65 6407 0167 E: [hidden email] W: www.a-star.edu.sg/imb/Tech-Platforms/AMP-Light-Microscopy |
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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. ***** To add: Where you can also combine TagBFP + eGFP/Venus + Tetra-methyl Rhodamine (TMR), in case you are able to add labelled dextrans for instance, to excite 3 dyes with 830-840nm Best Gabriel -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Ekaterina PAPUSHEVA Sent: Tuesday, October 16, 2018 15:43 To: [hidden email] Subject: Re: FPs for MP ***** 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. ***** BFP/GFP and BFP/YFP worked well with 800-820 nm excitation in Zebrafish. Good luck! Ekaterina -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Graham Wright Sent: Tuesday, October 16, 2018 3:38 PM To: [hidden email] Subject: FPs for MP ***** 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 all, I'm keen to find out what your favoured pair of fluorescent proteins for multiphoton microcopy, in which you’re limited to a single excitation wavelength (to avoid compromising too much with each). And which excitation wavelengths you use with them. Thanks in advance, Graham — Graham Wright, PhD Director, A*STAR Microscopy Platform T: +65 6407 0167 E: [hidden email] W: www.a-star.edu.sg/imb/Tech-Platforms/AMP-Light-Microscopy |
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