We have constructed a mathematical model to analyze the photon efficiency of frequency-domain fluorescence lifetime imaging microscopy (FLIM). The power of the light source needed for illumination in a FLIM system and the signal-to-noise ratio of the detector have led us to a photon “budget.” These measures are relevant to many fluorescence microscope users and the results are not restricted to FLIM but applicable to widefield fluorescence microscopy in general. Limitations in photon numbers, however, are more of an issue with FLIM compared to other less quantitative types of imaging. By modeling a typical experimental configuration, examples are given for fluorophores whose absorption peaks span the visible spectrum from Fura-2 to Cy5. We ...
In this paper a detailed discussion is presented of the factors that affect the fluorescence lifetim...
FRET measurements can provide dynamic spatial information on length scales smaller than the diffract...
The work presented here improves the level of quantification achievable with fluorescence microscopy...
We have constructed a mathematical model to analyze the photon efficiency of frequency-domain fluore...
Fluorescence lifetime imaging (FLIM) is a powerful microscopy technique for providing contrast of bi...
Fluorescence lifetime imaging (FLIM) is a powerful microscopy technique for providing contrast of bi...
Förster resonance energy transfer (FRET) imaging is an essential analytical method in biomedical res...
Förster resonance energy transfer (FRET) imaging is an essential analytical method in biomedical res...
Fluorescence lifetime imaging microscopy (FLIM) has become a standard tool in the quantitative chara...
Fluorescence lifetime imaging (FLIM) uses the fact that the fluorescence lifetime of a fluorophore d...
Fluorescence lifetime imaging microscopy (FLIM) may reveal subcellular spatial lifetime maps of key ...
Fluorescence lifetime images are obtained with the laser scanning microscope using two methods: the ...
Fluorescence lifetime images are obtained with the laser scanning microscope using two methods: the ...
We present novel Bayesian methods for the analysis of exponential decay data that exploit the eviden...
In this paper a detailed discussion is presented of the factors that affect the fluorescence lifetim...
In this paper a detailed discussion is presented of the factors that affect the fluorescence lifetim...
FRET measurements can provide dynamic spatial information on length scales smaller than the diffract...
The work presented here improves the level of quantification achievable with fluorescence microscopy...
We have constructed a mathematical model to analyze the photon efficiency of frequency-domain fluore...
Fluorescence lifetime imaging (FLIM) is a powerful microscopy technique for providing contrast of bi...
Fluorescence lifetime imaging (FLIM) is a powerful microscopy technique for providing contrast of bi...
Förster resonance energy transfer (FRET) imaging is an essential analytical method in biomedical res...
Förster resonance energy transfer (FRET) imaging is an essential analytical method in biomedical res...
Fluorescence lifetime imaging microscopy (FLIM) has become a standard tool in the quantitative chara...
Fluorescence lifetime imaging (FLIM) uses the fact that the fluorescence lifetime of a fluorophore d...
Fluorescence lifetime imaging microscopy (FLIM) may reveal subcellular spatial lifetime maps of key ...
Fluorescence lifetime images are obtained with the laser scanning microscope using two methods: the ...
Fluorescence lifetime images are obtained with the laser scanning microscope using two methods: the ...
We present novel Bayesian methods for the analysis of exponential decay data that exploit the eviden...
In this paper a detailed discussion is presented of the factors that affect the fluorescence lifetim...
In this paper a detailed discussion is presented of the factors that affect the fluorescence lifetim...
FRET measurements can provide dynamic spatial information on length scales smaller than the diffract...
The work presented here improves the level of quantification achievable with fluorescence microscopy...