Eric Olson |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear List, We are imaging cortical neurons in a transgenic mouse embryo (eGFP expressing). We can express a second FP by electroporation and want to visualize both FPs at one excitation wavelength. Any recommendations for another FP partner for eGFP? Possibly DsRed? And what excitation wavelength is used to excite both FPs? Our Chameleon laser tunes 700 to 950nm, but without much energy at the longer wavelengths. Thanks, Eric Eric C. Olson, Ph.D. Department of Neuroscience and Physiology SUNY Upstate Medical University 3295 Weiskotten Hall 766 Irving St. Syracuse, NY 13210 |
Pascal Weber |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** We use on our setup (Zeiss + MaïTaï) 840 or 930nm Cheers |
Andrew York |
In reply to this post by Eric Olson
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** No personal experience, but these links seem relevant: dx.doi.org/10.1038/nmeth0508-373 dx.doi.org/10.1038/nmeth.1596 On Fri, Apr 13, 2012 at 11:21 AM, Eric Olson <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Dear List, > > We are imaging cortical neurons in a transgenic mouse embryo (eGFP > expressing). We can express a second FP by electroporation and want to > visualize both FPs at one excitation wavelength. > > Any recommendations for another FP partner for eGFP? Possibly DsRed? And > what excitation wavelength is used to excite both FPs? Our Chameleon laser > tunes 700 to 950nm, but without much energy at the longer wavelengths. > > Thanks, > > Eric > > > Eric C. Olson, Ph.D. > Department of Neuroscience and Physiology > SUNY Upstate Medical University > 3295 Weiskotten Hall > 766 Irving St. > Syracuse, NY 13210 > |
Armstrong, Brian |
In reply to this post by Eric Olson
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Eric, we have good results with 860nm for dual green/red, and would suggest GFP and mCherry. Cheers, Brian D Armstrong PhD Assistant Research Professor Director, Light Microscopy Core Beckman Research Institute City of Hope Dept of Neuroscience 1450 E Duarte Rd Duarte, CA 91010 626-256-4673 x62872 http://www.cityofhope.org/research/support/Light-Microscopy-Digital-Imaging/Pages/default.aspx -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Eric Olson Sent: Friday, April 13, 2012 8:22 AM To: [hidden email] Subject: Optimal two-photon dual-color imaging using eGFP and . . . .? ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear List, We are imaging cortical neurons in a transgenic mouse embryo (eGFP expressing). We can express a second FP by electroporation and want to visualize both FPs at one excitation wavelength. Any recommendations for another FP partner for eGFP? Possibly DsRed? And what excitation wavelength is used to excite both FPs? Our Chameleon laser tunes 700 to 950nm, but without much energy at the longer wavelengths. Thanks, Eric Eric C. Olson, Ph.D. Department of Neuroscience and Physiology SUNY Upstate Medical University 3295 Weiskotten Hall 766 Irving St. Syracuse, NY 13210 --------------------------------------------------------------------- *SECURITY/CONFIDENTIALITY WARNING: This message and any attachments are intended solely for the individual or entity to which they are addressed. This communication may contain information that is privileged, confidential, or exempt from disclosure under applicable law (e.g., personal health information, research data, financial information). Because this e-mail has been sent without encryption, individuals other than the intended recipient may be able to view the information, forward it to others or tamper with the information without the knowledge or consent of the sender. If you are not the intended recipient, or the employee or person responsible for delivering the message to the intended recipient, any dissemination, distribution or copying of the communication is strictly prohibited. If you received the communication in error, please notify the sender immediately by replying to this message and deleting the message and any accompanying files from your system. If, due to the security risks, you do not wish to receive further communications via e-mail, please reply to this message and inform the sender that you do not wish to receive further e-mail from the sender. (fpc5p) --------------------------------------------------------------------- |
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