Fluorescence Spectroscopy and Microscopy Methods and Protocols 1st Edition by Yves Engelborghs, Antonie Visser – Ebook PDF Instant Download/Delivery: 9781627036498, 1627036490
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Product details:
ISBN 10: 1627036490
ISBN 13: 9781627036498
Author: Yves Engelborghs, Antonie J.W.G. Visser
Reflecting the expanding field’s need for reliable protocols, __Fluorescence Spectroscopy and Microscopy: Methods and Protocols__ offers techniques from a worldwide team of experts on this versatile and vital subject. The topics covered fall into four broad categories: steady-state fluorescence spectroscopy, time-resolved fluorescence spectroscopy, fluorescent probe development, and the various sub-categories of fluorescence microscopy, such as fluorescence recovery after photobleaching (FRAP), live cell FRET imaging (FRETim), fluorescence lifetime imaging (FLIM), fluorescence fluctuation spectroscopy (FFS), and single-molecule fluorescence spectroscopy (smFS). Written as a part of the popular __Methods in Molecular Biology__ series, chapters include the kind of unambiguous detail and key implementation advice that proves essential for successful results.
Comprehensive and practical, __Fluorescence Spectroscopy and Microscopy: Methods and Protocols__ aims to guide both ‘novice’ and established scientists toward furthering their research with these invaluable techniques.
Table of contents:
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How to Collect National Institute of Standards and Technology (NIST) Traceable Fluorescence Excitation and Emission Spectra
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Steady-State Fluorescence Polarization/Anisotropy for the Study of Protein Interactions
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Quantitative Fluorescence Spectral Analysis of Protein Denaturation
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High-Pressure Fluorescence Applications
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Frequency Domain Fluorometry: Theory and Application
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Polar Plot Representation of Time-Resolved Fluorescence
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Ensemble and Single-Molecule Detected Time-Resolved FRET Methods in Studies of Protein Conformations and Dynamics
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MD + QM Correlations with Tryptophan Fluorescence Spectral Shifts and Lifetimes
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Analysis of Time-Dependent Red Shifts in Fluorescence Emission from Tryptophan Residues in Proteins
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Global Analysis of Time-Resolved Fluorescence Data
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Nanometrology
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Upconversion Spectrophotofluorometry
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Subpicosecond Kerr-Gate Spectrofluorometry
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Photoinduced Electron Transfer Modeling to Simulate Flavoprotein Fluorescence Decay
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Biosynthetic Incorporation of Tryptophan Analogs in Proteins
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Optimization of Fluorescent Proteins
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Monitoring Membrane Properties and Apoptosis Using Membrane Probes of the 3-Hydroxyflavone Family
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Rectangle FRAP for Measuring Diffusion with a Laser Scanning Microscope
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Quantitative Protocol for Intensity-Based Live Cell FRET Imaging
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Wide-Field Fluorescence Lifetime Imaging with Multi-Anode Detectors
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Global Analysis of FRET-FLIM Data in Live Plant Cells
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Time-Resolved Fluorescence Anisotropy Imaging
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Multimodal Fluorescence Imaging Spectroscopy
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Application of Fluorescence Correlation Spectroscopy (FCS) to Measure the Dynamics of Fluorescent Proteins in Living Cells
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Fluorescence Cross-Correlation Spectroscopy (FCCS) in Living Cells
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Quantifying Lipid-Protein Interaction by Fluorescence Correlation Spectroscopy (FCS)
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PET-FCS: Probing Rapid Structural Fluctuations of Proteins and Nucleic Acids by Single-Molecule Fluorescence Quenching
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Z-Scan Fluorescence Correlation Spectroscopy as a Tool for Diffusion Measurements in Planar Lipid Membranes
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Scanning Fluorescence Correlation Spectroscopy (SFCS) with a Scan Path Perpendicular to the Membrane Plane
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Implementation and Application of Pulsed Interleaved Excitation for Dual-Color FCS and RICS
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Quantitative Study of Protein-Protein Interactions in Live Cell by Dual-Color Fluorescence Correlation Spectroscopy
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Brightness Experiments
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Global Analysis of Autocorrelation Functions and Photon Counting Distributions in Fluorescence Fluctuation Spectroscopy
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Simulation of Autocorrelation Function and Photon Counting Distribution in Fluorescence Fluctuation Spectroscopy
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Single-Molecule Fluorescence of Nucleic Acids
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Photoswitchable Fluorescent Proteins for Superresolution Fluorescence Microscopy Circumventing the Diffraction Limit of Light
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Tags: Yves Engelborghs, Antonie Visser, Fluorescence, Microscopy