A Feasible Add-On Upgrade on a Commercial Two-Photon FLIM Microscope for Optimal FLIM-FRET Imaging of CFP-YFP Pairs
暂无分享,去创建一个
[1] M. Davidson,et al. An Improved Cerulean Fluorescent Protein with Enhanced Brightness and Reduced Reversible Photoswitching , 2011, PloS one.
[2] A. Pietraszewska-Bogiel,et al. FRET microscopy: from principle to routine technology in cell biology , 2011, Journal of microscopy.
[3] S. Achilefu,et al. Fluorescence lifetime measurements and biological imaging. , 2010, Chemical reviews.
[4] Rory R. Duncan,et al. Munc18/Syntaxin Interaction Kinetics Control Secretory Vesicle Dynamics* , 2009, The Journal of Biological Chemistry.
[5] Jörg Enderlein,et al. Remote temperature measurements in femto-liter volumes using dual-focus-Fluorescence Correlation Spectroscopy. , 2009, Lab on a chip.
[6] Paolo Fornasini,et al. The Uncertainty in Physical Measurements: An Introduction to Data Analysis in the Physics Laboratory , 2008 .
[7] H. Ewers,et al. Even illumination in total internal reflection fluorescence microscopy using laser light , 2008, Microscopy research and technique.
[8] D. Piston,et al. Fluorescent protein FRET: the good, the bad and the ugly. , 2007, Trends in biochemical sciences.
[9] R. Zucker,et al. Quality assessment of confocal microscopy slide based systems: Performance , 2006, Cytometry. Part A : the journal of the International Society for Analytical Cytology.
[10] W. Zipfel,et al. Optimization of Pairings and Detection Conditions for Measurement of FRET between Cyan and Yellow Fluorescent Proteins , 2006, Microscopy and Microanalysis.
[11] W. Becker. Advanced Time-Correlated Single Photon Counting Techniques , 2005 .
[12] G. Karp. Cell and molecular biology : concepts and experiments / Gerald Karp , 1996 .