Abstract
Spectrally Resolved Fluorescence Lifetime Imaging Microscopy (SFLIM), that uses a standard confocal microscope for imaging single molecules in living cells was presented. The fluorescence lifetime images were generated by recording the signals from two avalanche photodiodes by time-correlated single-photon counting interface card. The image signal data to determine monoexponential fluorescence lifetimes from a low photon statistics, was analyzed by applying a maximum likelihood estimator (MLE) a
Sprache: English
Art der Begutachtung: Peer Review(Double-blind peer review)
Print: Ja
Online: Ja, ohne Open Access
Datenmedium: Keine Angabe
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