Rapid fluorescence lifetime imaging microscopy via few-photon imaging
Conventional fluorescence lifetime imaging microscopy (FLIM) based on time-correlated single photon counting has great potential in various domains, notably in cellular biology, enabling comprehensive studies encompassing spatiotemporal dynamics and quantitative analysis of fluorescence lifetimes. H...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
AIP Publishing LLC
2024-01-01
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| Series: | APL Photonics |
| Online Access: | http://dx.doi.org/10.1063/5.0178452 |