Graham Wright-2 |
*****
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. ***** Hello, I would like to ask for some opinions/feedback from those with experience of using ATTO488 and ATTO565 for live-cell imaging experiments (conjugated to peptides), particularly in terms of photostability/bleaching (planned for WF and spinning disk microscopy). I heard from someone that the ATTO565 bleaches relatively quickly (not sure on their imaging parameters), but would like to hear more. Would people recommend any other dyes in this spectral range (561 nm laser) that they have used for these sort of experiments? Thanks in advance, Graham -- Graham Wright, PhD Head, Microscopy Unit Institute of Medical Biology, A*STAR 8A Biomedical Grove, #06-06 Immunos, Singapore 138648 W: http://www.a-star.edu.sg/imb/Tech-Platforms/IMB-Microscopy-Unit.aspx |
lechristophe |
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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 Graham, This reference could be useful: Bosch PJ, Corrêa IR, Sonntag MH, Ibach J, Brunsveld L, Kanger JS & Subramaniam V (2014) Evaluation of Fluorophores to Label SNAP-Tag Fused Proteins for Multicolor Single-Molecule Tracking Microscopy in Live Cells. *Biophys. J* *107:* 803–814 They have tested 6 green and 16 red dyes for single molecule tracking in live cells. Hope this helps, Christophe On Fri, Jun 19, 2015 at 10:25 AM, Graham Wright <[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. > ***** > > Hello, > > I would like to ask for some opinions/feedback from those with experience > of using ATTO488 and ATTO565 for live-cell imaging experiments (conjugated > to peptides), particularly in terms of photostability/bleaching (planned > for WF and spinning disk microscopy). > > I heard from someone that the ATTO565 bleaches relatively quickly (not sure > on their imaging parameters), but would like to hear more. Would people > recommend any other dyes in this spectral range (561 nm laser) that they > have used for these sort of experiments? > > Thanks in advance, > Graham > > -- > Graham Wright, PhD > Head, Microscopy Unit > > Institute of Medical Biology, A*STAR > 8A Biomedical Grove, #06-06 Immunos, Singapore 138648 > > W: http://www.a-star.edu.sg/imb/Tech-Platforms/IMB-Microscopy-Unit.aspx > |
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