edited by Peter J. Verveer, Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany
PHYSICAL DESCRIPTION
Specific Material Designation and Extent of Item
xi, 294 pages : illustrations )some color( ;
SERIES
Series Title
Methods in molecular biology,1064-3745 ;1251
Series Title
Springer protocols
Series Title
Series: Methods in molecular biology )Clifton, N.J.( ;v. 1251.1064-3745
Series Title
Series: Springer protocols )Series(
CONTENTS NOTE
Text of Note
The physical basis of total internal reflection fluorescence )TIRF( microscopy and its cellular applications --Two-photon excitation microscopy and its applications in neuroscience --Live spheroid formation recorded with light sheet-based fluorescence microscopy --Fluorescence microscopy-based RNA interference screening --Fluorescence resonance energy transfer microscopy )FRET( --Localizing protein-protein interactions in living cells using fluorescence lifetime imaging microscopy --Analysis of biomolecular dynamics by FRAP and computer simulation --Fluorescence correlation spectroscopy --Homo-FRET imaging highlights the nanoscale organization of cell surface molecules --Practical structured illumination microscopy -- 4Pi microscopy of the nuclear pore complex --Application of STED microscopy to cell biology questions --Three-dimensional photoactivated localization microscopy with genetically expressed probes --Direct stochastic optical reconstruction microscopy )dSTORM( --Optogenetics: Optical control of a photoactivatable Rac in living cells.