Presentation
9 March 2020 Fluorescence lifetime image scanning microscopy (Conference Presentation)
Ingo Gregor, Niels Radmacher, Jörg Enderlein
Author Affiliations +
Abstract
Image Scanning Microscopy (ISM) enhances the spatial resolution of a confocal microscope by simple means. An extension to realize fluorescence lifetime imaging in combination with ISM seems straight-forward. First realizations have been reported by Israel et al. and Castello et al. [1,2] Here, we present a cost-efficient detector scheme based on a commercial multi-anode PMT that allows to perform fluorescence lifetime imaging microscopy (FLIM) in combination with ISM. We developa dedicated amplification electronics that allows for counting signals from 32 detector pixels using a commercial eight channel TCSPC hardware. [1] Y. Israel, R. Tenne, D. Oron, and Y. Silberberg “Quantum correlation enhanced super-resolution localization microscopy enabled by a fibre bundle camera” Nat. Commun. 8 (2017) 14786. [2] M. Castello et al. “A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM” Nat. Methods 16 (2019) 175-178.
Conference Presentation
© (2020) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Ingo Gregor, Niels Radmacher, and Jörg Enderlein "Fluorescence lifetime image scanning microscopy (Conference Presentation)", Proc. SPIE 11246, Single Molecule Spectroscopy and Superresolution Imaging XIII, 1124606 (9 March 2020); https://doi.org/10.1117/12.2546532
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KEYWORDS
Microscopy

Fluorescence lifetime imaging

Sensors

Luminescence

Confocal microscopy

Cameras

Electronics

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