Implementing Fluorescence Lifetime Imaging on a Confocal Microscope

碩士 === 國立中山大學 === 光電工程研究所 === 93 === In this thesis, the development and implementation of fluorescence lifetime imaging microscopy that integrates time correlated single photon counting (TCSPC) and a confocal microscope will be described. The TCSPC method has high detection efficiency, with a time...

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Main Authors: Yi-Chun Chiu, 邱一鈞
Other Authors: Fu-Jen Kao
Format: Others
Language:zh-TW
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/99199009215630318239
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spelling ndltd-TW-093NSYS51240172015-12-23T04:08:13Z http://ndltd.ncl.edu.tw/handle/99199009215630318239 Implementing Fluorescence Lifetime Imaging on a Confocal Microscope 以共焦顯微鏡建構螢光半衰期影像系統 Yi-Chun Chiu 邱一鈞 碩士 國立中山大學 光電工程研究所 93 In this thesis, the development and implementation of fluorescence lifetime imaging microscopy that integrates time correlated single photon counting (TCSPC) and a confocal microscope will be described. The TCSPC method has high detection efficiency, with a time resolution limited only by the transit time spread of the detector, and directly delivers the decay functions in the time domain. TCSPC can also be used to obtain images that indicate the fluorescence resonance energy transfer (FRET) effect between critical fluorophores, an important method distinguish the difference between binding and co-localization. Estimation of distances between RET fluorophore pairs can also be established. Additionally, the effects of ion concentration, oxygen concentration, pH value, ..etc. can also be revealed. Fu-Jen Kao 高甫仁 2005 學位論文 ; thesis 64 zh-TW
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description 碩士 === 國立中山大學 === 光電工程研究所 === 93 === In this thesis, the development and implementation of fluorescence lifetime imaging microscopy that integrates time correlated single photon counting (TCSPC) and a confocal microscope will be described. The TCSPC method has high detection efficiency, with a time resolution limited only by the transit time spread of the detector, and directly delivers the decay functions in the time domain. TCSPC can also be used to obtain images that indicate the fluorescence resonance energy transfer (FRET) effect between critical fluorophores, an important method distinguish the difference between binding and co-localization. Estimation of distances between RET fluorophore pairs can also be established. Additionally, the effects of ion concentration, oxygen concentration, pH value, ..etc. can also be revealed.
author2 Fu-Jen Kao
author_facet Fu-Jen Kao
Yi-Chun Chiu
邱一鈞
author Yi-Chun Chiu
邱一鈞
spellingShingle Yi-Chun Chiu
邱一鈞
Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
author_sort Yi-Chun Chiu
title Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
title_short Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
title_full Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
title_fullStr Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
title_full_unstemmed Implementing Fluorescence Lifetime Imaging on a Confocal Microscope
title_sort implementing fluorescence lifetime imaging on a confocal microscope
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/99199009215630318239
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