Spectral imaging fluorescence microscopy

被引:101
作者
Haraguchi, T
Shimi, T
Koujin, T
Hashiguchi, N
Hiraoka, Y
机构
[1] Kansai Adv Res Ctr, CREST Res Project, Commun Res Lab, Kobe, Hyogo, Japan
[2] Osaka Univ, Dept Biol, Grad Sch Sci, Osaka 5600043, Japan
关键词
D O I
10.1046/j.1365-2443.2002.00575.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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).
引用
收藏
页码:881 / 887
页数:7
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