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Multi-Parametric Live Cell Microscopy of 3D Tissue Models

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Attention for Chapter 8: Application of Fluorescence Lifetime Imaging (FLIM) to Measure Intracellular Environments in a Single Cell
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Chapter title
Application of Fluorescence Lifetime Imaging (FLIM) to Measure Intracellular Environments in a Single Cell
Chapter number 8
Book title
Multi-Parametric Live Cell Microscopy of 3D Tissue Models
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-3-319-67358-5_8
Pubmed ID
Book ISBNs
978-3-31-967357-8, 978-3-31-967358-5
Authors

Takakazu Nakabayashi, Kamlesh Awasthi, Nobuhiro Ohta

Abstract

Fluorescence 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.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Professor > Associate Professor 3 27%
Student > Doctoral Student 1 9%
Student > Ph. D. Student 1 9%
Professor 1 9%
Researcher 1 9%
Other 1 9%
Unknown 3 27%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 45%
Agricultural and Biological Sciences 1 9%
Physics and Astronomy 1 9%
Medicine and Dentistry 1 9%
Unknown 3 27%