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dc.contributor.authorNakabayashi, Takakazuen_US
dc.contributor.authorAwasthi, Kamleshen_US
dc.contributor.authorOhta, Nobuhiroen_US
dc.date.accessioned2018-08-21T05:53:51Z-
dc.date.available2018-08-21T05:53:51Z-
dc.date.issued2017-01-01en_US
dc.identifier.issn0065-2598en_US
dc.identifier.urihttp://dx.doi.org/10.1007/978-3-319-67358-5_8en_US
dc.identifier.urihttp://hdl.handle.net/11536/145247-
dc.description.abstractFluorescence lifetime imaging (FLIM) has now been used in many bioscience fields, which comes from the quantification of fluorescence lifetime. The procedure for obtaining lifetime images is very similar to that used in fluorescence microscopy. However, obtaining reliable lifetime images requires an understanding of the theory of fluorescence lifetime, principle of FLIM systems, and evaluation procedure of intracellular environments. In this chapter, the materials, methods, and notes on FLIM measurements have been described, in conjunction with a brief explanation of the background of FLIM.en_US
dc.language.isoen_USen_US
dc.subjectFluorescence lifetime imagingen_US
dc.subjectTCSPCen_US
dc.subjectFemtosecond laseren_US
dc.subjectIntracellular pHen_US
dc.subjectIntracellular environmenten_US
dc.subjectRatiometric methoden_US
dc.titleApplication of Fluorescence Lifetime Imaging (FLIM) to Measure Intracellular Environments in a Single Cellen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/978-3-319-67358-5_8en_US
dc.identifier.journalMULTI-PARAMETRIC LIVE CELL MICROSCOPY OF 3D TISSUE MODELSen_US
dc.citation.volume1035en_US
dc.citation.spage121en_US
dc.citation.epage133en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000438285400009en_US
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