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Spectral imaging fluorescence microscopy | |
Haraguchi, T. | |
2002 | |
Source Publication | Genes to Cells
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ISSN | 1356-9597 |
Volume | 7Issue:9Pages:881-887 |
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). |
Language | 英语 |
Document Type | 期刊论文 |
Identifier | https://ir.xtbg.ac.cn/handle/353005/8963 |
Collection | 公共技术服务中心主要仪器相关文献_激光共聚焦显微镜 |
Recommended Citation GB/T 7714 | Haraguchi, T.. Spectral imaging fluorescence microscopy[J]. Genes to Cells,2002,7(9):881-887. |
APA | Haraguchi, T..(2002).Spectral imaging fluorescence microscopy.Genes to Cells,7(9),881-887. |
MLA | Haraguchi, T.."Spectral imaging fluorescence microscopy".Genes to Cells 7.9(2002):881-887. |
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