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Fluorescence Lifetime Imaging Microscopy

2019
FLIO is based on Fluorescence Lifetime Imaging Microscopy (FLIM), which is used in basic science to investigate metabolic conditions in cell cultures and tissues. After excitation of fluorophores with a laser light, the fluorophore returns to its ground state by releasing light with a longer wavelength.
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Fluorescence Lifetime Imaging Microscopy for Quantitative Biological Imaging

2013
Fluorescence lifetime imaging microscopy (FLIM) is a method for measuring fluorophore lifetimes with microscopic spatial resolution, providing a useful tool for cell biologists to detect, visualize, and investigate structure and function of biological systems. In this chapter, we begin by introducing the basic theory of fluorescence lifetime, including
Leng-Chun, Chen   +4 more
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Fluorescence Lifetime Imaging Microscopy: Two‐Dimensional Distribution Measurement of Fluorescence Lifetime

2006
A newly developed fluorescence lifetime imaging microscopy (FLIM) system has combined the high-temporal resolution of a streak camera with the high-spatial resolution of a microscope to obtain a two-dimensional distribution of fluorescence lifetimes within living cells. The temporal resolution is as short as 20 ps.
Masanobu, Fujiwara, William, Cieslik
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Applying image restoration to fluorescence lifetime imaging microscopy (FLIM)

SPIE Proceedings, 2009
We describe a novel approach using 2D-intensity-deconvolution to improve spatial resolution in wide-field FLIM. The method maintains lifetime accuracy and can restore features within experimentally reasonable intensity ranges.
Ching-Wei Chang, Mary-Ann Mycek
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Three dimensional image restoration in fluorescence lifetime imaging microscopy

Journal of Microscopy, 1999
A microscope set‐up and numerical methods are described which enable the measurement and reconstruction of three‐dimensional nanosecond fluorescence lifetime images in every voxel. The frequency domain fluorescence lifetime imaging microscope (FLIM) utilizes phase detection of high‐frequency modulated light by homodyne mixing on a microchannel plate ...
Squire, A., Bastiaens, P.
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Imaging Vacuolar Anthocyanins with Fluorescence Lifetime Microscopy (FLIM)

2018
Anthocyanins are intrinsically fluorescent pigments that accumulate in plant vacuoles. We have developed a platform to analyze the fluorescence decay of anthocyanins by fluorescence lifetime imaging microscopy (FLIM), under in vitro and in vivo conditions. Fluorescence lifetime of a fluorophore can be influenced by temperature, pH, oxygen concentration,
Alexandra, Chanoca   +4 more
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Fluorescence-lifetime image scanning microscopy

Improving optical resolution and image quality has always been an important goal in the field of microscopy. One technique that histori- cally played a major role in the optimization of image quality has been confocal microscopy. With the ability to remove out of focus contribu- tion to the final image it has revolutionized the field.
Radmacher, Niels Johann   +5 more
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Fluorescence Lifetime Imaging Microscopy (FLIM): Instrumentation and Applications

Critical Reviews in Analytical Chemistry, 1992
Ammasi Periasamy   +2 more
exaly  

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