Related Experiment Video
Updated: Jan 19, 2026

Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
Published on: December 29, 2017
Cramér-Rao analysis of lifetime estimations in time-resolved fluorescence microscopy
Abstract:
Measuring the lifetime of fluorescent emitters by time-correlated single photon counting (TCSPC) is a routine procedure in many research areas spanning from nanophotonics to biology. The precision of such measurement depends on the number of detected photons but also on the various sources of noise arising from the measurement process. Using Fisher information theory, we calculate the lower bound on the precision of lifetime estimations for mono-exponential and bi-exponential distributions. We analyse the dependence of the lifetime estimation precision on experimentally relevant parameters, including the contribution of a non-uniform background noise and the instrument response function (IRF) of the setup. We also provide an open-source code to determine the lower bound on the estimation precision for any experimental conditions. Two practical examples illustrate how this tool can be used to reach optimal precision in time-resolved fluorescence microscopy.
Related Concept Videos
08:55Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy
09:30Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
06:01Fluorescence Lifetime Macro Imager for Biomedical Applications
Analyzing Amyloid Structures in a Tissue Section Using Fluorescence Lifetime Imaging Microscopy
10:23Time-Resolved Fluorescence Anisotropy from Single Molecules for Characterizing Local Flexibility in Biomolecules
08:43Production and Multi-Parameter Live Cell Fluorescence Lifetime Imaging Microscopy (FLIM) of Multicellular Spheroids

