| Literature DB >> 27088314 |
Marcel Raspe1, Katarzyna M Kedziora1, Bram van den Broek1, Qiaole Zhao2, Sander de Jong3, Johan Herz3, Marieke Mastop4, Joachim Goedhart4,5, Theodorus W J Gadella4,5, Ian T Young2, Kees Jalink1,4,5.
Abstract
We developed single-image fluorescence lifetime imaging microscopy (siFLIM), a method for acquiring quantitative lifetime images from a single exposure. siFLIM takes advantage of a new generation of dedicated cameras that simultaneously record two 180°-phase-shifted images, and it allows for video-rate lifetime imaging with minimal phototoxicity and bleaching. siFLIM is also inherently immune to artifacts stemming from rapid cellular movements and signal transients.Mesh:
Substances:
Year: 2016 PMID: 27088314 DOI: 10.1038/nmeth.3836
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547