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A method for the fast and photon‐efficient analysis of time‐domain fluorescence lifetime image data over large dynamic ranges

Fluorescence lifetime imaging (FLIM) allows the quantification of sub‐cellular processes in situ, in living cells. A number of approaches have been developed to extract the lifetime from time‐domain FLIM data, but they are often limited in terms of speed, photon efficiency, precision or the dynamic...

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Detalles Bibliográficos
Autores principales:	Laine, Romain F., Poudel, Chetan, Kaminski, Clemens F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544871/ https://www.ncbi.nlm.nih.gov/pubmed/35676768 http://dx.doi.org/10.1111/jmi.13128

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