Additional content from Coherent Corp
Additional content from Coherent Corp
(Photo credit: SPIE)
(Courtesy of R. Kato/Tokushima University)
Photo 237017308 © Penchan Pumila | Dreamstime.com
(Courtesy of Frank Lison, Toptica)
(Photo 100051973 © Keatanan Viya | Dreamstime.com)
(Photo 139452497 © Ecaterina Tolicova | Dreamstime.com)
(Photo 138242136 © Feng Yu | Dreamstime.com)
(Photo 70224198 © One Photo | Dreamstime.com)
(Photo 181453982 © Andrey Popov | Dreamstime.com)
(ID: 180682420 © Tero Vesalainen | Dreamstime.com)
(Credit: Gerd Altmann/Pixabay)
(Courtesy of Morgan Trassin)
Credit: Gerd Altmann/Pixabay
(Courtesy of the Fleming group)
![FIGURE 1. These total internal reflection fluorescence microscopy images were obtained using two excitation lasers combined in the Coherent Galaxy laser combiner; as part of research on the binding of actin filaments, the red signal is from Cy5-labeled Tm1A (protein) fluorescence excited at 640 nm, and the green signal is due to Alexa488 labeled actin excited at 488 nm. [1]](https://img.laserfocusworld.com/files/base/ebm/lfw/image/2018/07/content_dam_lfw_print_articles_2018_06_1806lfw_cal_f1.png?auto=format,compress&fit=&q=45&h=139&height=139&w=250&width=250 "FIGURE 1. These total internal reflection fluorescence microscopy images were obtained using two excitation lasers combined in the Coherent Galaxy laser combiner; as part of research on the binding of actin filaments, the red signal is from Cy5-labeled Tm1A (protein) fluorescence excited at 640 nm, and the green signal is due to Alexa488 labeled actin excited at 488 nm. [1]")
(Courtesy of Becton Dickinson)
(Courtesy of IPG Photonics)
(Courtesy of Gentec-EO USA)
(Courtesy of Adam Packer, Häusser lab, University College London)
(Courtesy Christian Eggeling and Alf Honigman)
(Images courtesy of the Campagnola lab, University of Wisconsin-Madison)
