| Literature DB >> 12296819 |
Tokuko Haraguchi1, Takeshi Shimi, Takako Koujin, Noriyo Hashiguchi, Yasushi Hiraoka.
Abstract
The spectral resolution of fluorescence microscope images in living cells is achieved by using a confocal laser scanning microscope equipped with grating optics. This capability of temporal and spectral resolution is especially useful for detecting spectral changes of a fluorescent dye; for example, those associated with fluorescence resonance energy transfer (FRET). Using the spectral imaging fluorescence microscope system, it is also possible to resolve emitted signals from fluorescent dyes that have spectra largely overlapping with each other, such as fluorescein isothiocyanate (FITC) and green fluorescent protein (GFP).Entities:
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Year: 2002 PMID: 12296819 DOI: 10.1046/j.1365-2443.2002.00575.x
Source DB: PubMed Journal: Genes Cells ISSN: 1356-9597 Impact factor: 1.891