Visualizing dynamic processes with rapidFLIMHiRes, the ultra fast FLIM imaging method with outstanding 10ps time resolution

Maria Loidolt-Krüger; Fabian Jolmes; Matthias Patting; Michael Wahl; Evangelos Sisamakis; André Devaux; Uwe Ortmann; Felix Koberling; Rainer Erdmann

doi:10.1364/OMP.2021.OTh1E.5

Biophotonics Congress 2021
OSA Technical Digest (Optica Publishing Group, 2021),
paper OTh1E.5
•https://doi.org/10.1364/OMP.2021.OTh1E.5

Visualizing dynamic processes with rapidFLIM^HiRes, the ultra fast FLIM imaging method with outstanding 10ps time resolution

Maria Loidolt-Krüger, Fabian Jolmes, Matthias Patting, Michael Wahl, Evangelos Sisamakis, André Devaux, Uwe Ortmann, Felix Koberling, and Rainer Erdmann

Optical Molecular Probes, Imaging and Drug Delivery 2021

Washington, DC United States
12–16 April 2021
ISBN: 978-1-943580-85-9

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Biomolecular Processes (OTh1E)

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M. Loidolt-Krüger, F. Jolmes, M. Patting, M. Wahl, E. Sisamakis, A. Devaux, U. Ortmann, F. Koberling, and R. Erdmann, "Visualizing dynamic processes with rapidFLIMHiRes, the ultra fast FLIM imaging method with outstanding 10ps time resolution," in Biophotonics Congress 2021, C. Boudoux, K. Maitland, C. Hendon, M. Wojtkowski, K. Quinn, M. Schanne-Klein, N. Durr, D. Elson, F. Cichos, L. Oddershede, V. Emiliani, O. Maragò, S. Nic Chormaic, N. Pégard, S. Gibbs, S. Vinogradov, M. Niedre, K. Samkoe, A. Devor, D. Peterka, P. Blinder, and E. Buckley, eds., OSA Technical Digest (Optica Publishing Group, 2021), paper OTh1E.5.

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Abstract

PicoQuant’s rapidFLIM^HiRes approach redefines Fluorescence Lifetime Imaging (FLIM). Combining fast data acquisition with 10 ps time resolution allows for reliable, quantitative analysis of fast processes like protein interactions, changes in environmental parameters, or metabolic imaging.

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