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Published in 2022 at "Analytical chemistry"
DOI: 10.1021/acs.analchem.2c02149
Abstract: The excited-state lifetime is an intrinsic property of fluorescent molecules that can be leveraged for multiplexed imaging. An advantage of fluorescence lifetime-based multiplexing is that signals from multiple probes can be gathered simultaneously, whereas traditional…
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Keywords:
three probes;
fluorescence lifetime;
phasor analysis;
lifetime ... See more keywords
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3
Published in 2023 at "Analytical Chemistry"
DOI: 10.1021/acs.analchem.3c00212
Abstract: Hyperspectral stimulated Raman scattering (SRS) microscopy is a robust imaging tool for the analysis of biological systems. Here, we present a unique perspective, a label-free spatiotemporal map of mitosis, by integrating hyperspectral SRS microscopy with…
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Keywords:
label free;
mitosis;
spectral phasor;
microscopy ... See more keywords
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Published in 2022 at "Molecular biology of the cell"
DOI: 10.1091/mbc.p22-04-1006
Abstract: Luciferaseābased bioluminescence imaging requires no excitation light and thus can be advantageous over fluorescence imaging, but multicolor imaging has been a challenge due to the difficulties of spectral and substrate unmixing. To achieve effective multiplexing…
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Keywords:
bioluminescence;
cell;
microscopy;
phasor analysis ... See more keywords
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Published in 2022 at "Optics express"
DOI: 10.1364/oe.450761
Abstract: We investigated the possibility of using long excitation pulses in fluorescence lifetime imaging microscopy (FLIM) using phasor analysis. It has long been believed that the pulse width of an excitation laser must be shorter than…
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Keywords:
measurement;
excitation;
excitation pulses;
phasor analysis ... See more keywords