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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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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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.
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Fu-Jen Kao |
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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 |
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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 |
work_keys_str_mv |
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