Results 151 to 160 of about 6,539 (187)
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mb-FLIM: Model-based fluorescence lifetime imaging
SPIE Proceedings, 2012We have developed a model-based, parallel procedure to estimate fluorescence lifetimes. Multiple frequencies are present in the excitation signal. Modeling the entire fluorescence and measurement process produces an analytical ratio of polynomials in the lifetime variable τ. A non-linear model-fitting procedure is then used to estimate τ.
Qiaole Zhao +5 more
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Biophysical Chemistry, 1993
A frequency domain fluorescence lifetime imaging microscope (FLIM) has been developed. A continuous wave laser excitation source of an epi-illumination fluorescence microscope is modulated at a high frequency fk The lifetime of the modulated fluorescence emission is determined from the phase delay and modulation depth of the fluorescence signal ...
Thomas M Jovin +2 more
exaly +5 more sources
A frequency domain fluorescence lifetime imaging microscope (FLIM) has been developed. A continuous wave laser excitation source of an epi-illumination fluorescence microscope is modulated at a high frequency fk The lifetime of the modulated fluorescence emission is determined from the phase delay and modulation depth of the fluorescence signal ...
Thomas M Jovin +2 more
exaly +5 more sources
Fluorescence lifetime imaging microscopy (FLIM) on the single molecule level
Laser Applications to Chemical and Environmental Analysis, 2001During the last years, several methods for the detection of individual fluorescently labeled molecules have been developed.
Phillip Tinnefeld +4 more
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Fluorescence lifetime imaging (FLIM) of membrane markers in living cells
Confocal, Multiphoton, and Nonlinear Microscopic Imaging, 2003An experimental setup for fluorescence lifetime imaging (FLIM) has been combined with total internal reflection fluorescence microscopy (TIRFM) in order to detect various membrane markers within living cells. The method is established using T47D human breast cancer cells transfected by a plasmid encoding for a membrane associated yellow fluorescent ...
Herbert Schneckenburger +4 more
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SPIE Proceedings, 2006
We characterised populations of wild type baking and brewing yeast cells using intrinsic fluorescence and fluorescence lifetime microscopy, in order to obtain quantitative identifiers of different strains. The cell autofluorescence was excited at 405 nm and observed within 440-540 nm range where strong cell to cell variability was observed.
H. Bhatta, E. M. Goldys, J. Ma
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We characterised populations of wild type baking and brewing yeast cells using intrinsic fluorescence and fluorescence lifetime microscopy, in order to obtain quantitative identifiers of different strains. The cell autofluorescence was excited at 405 nm and observed within 440-540 nm range where strong cell to cell variability was observed.
H. Bhatta, E. M. Goldys, J. Ma
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Fluorescence Lifetime Imaging (FLIM): Basic Concepts and Recent Applications
2015Fluorescence lifetime imaging (FLIM) is a key fluorescence microscopy technique to map the environment and interaction of fluorescent probes. It can report on photo physical events that are difficult or impossible to observe by fluorescence intensity imaging, because FLIM is independent of the local fluorophore concentration and excitation intensity. A
Suhling, Klaus +12 more
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Analysis of Fluorescence Lifetime Imaging Microscopy (FLIM) Data
Methods of Information in Medicine, 2010Summary Objectives: A novel Fluorescence Lifetime Imaging Microscopy (FLIM) deconvolution method based on the linear expansion of fluorescence decays on a set of orthonormal Laguerre functions was recently proposed. The Laguerre deconvolution method applies linear least-square estimation to estimate the expansion coefficients of all pixel ...
P, Pande, C A, Trivedi, J A, Jo
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Fluorescence lifetime imaging (FLIM): Basic concepts and some recent developments
Medical Photonics, 2015Summary Fluorescence lifetime imaging (FLIM) is a key fluorescence microscopy technique to map the environment and interaction of fluorescent probes. It can report on photophysical events that are difficult or impossible to observe by fluorescence intensity imaging, because FLIM is independent of the local fluorophore concentration and excitation ...
Suhling, Klaus +12 more
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Fluorescence Resonance Energy Transfer (FRET) and Fluorescence Lifetime Imaging Microscopy (FLIM)
2006Current approaches and developments in the field of microscopy based on determinations of Fluorescence (Forster) Resonance Energy Transfer (FRET) and Fluorescence Lifetime (FLIM) are discussed.
Jovin, T., Lidke, D., Jares-Erijman, E.
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Confocal Fluorescence Lifetime Imaging Microscopy (FLIM) at the Single Molecule Level
Single Molecules, 2000We report on confocal fluorescence lifetime imaging microscopy (CFLIM) of single dye molecules adsorbed on glass surface. Applying a short-pulse diode laser emitting at 635 nm with a repetition rate of 64 MHz we studied the time-resolved identification of individual carbocyanine and oxazine dyes via their characteristic fluorescence lifetimes of 2.06±0.
Philip Tinnefeld +4 more
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