Photonic imaging for biology : from conventional microscopy to super-resolution
tarafından
 
Sibarita, Jean-Baptiste, editor.

Başlık
Photonic imaging for biology : from conventional microscopy to super-resolution

Yazar
Sibarita, Jean-Baptiste, editor.

ISBN
9781394417896
 
9781394417872

Fiziksel Tanımlama
1 online resource (257 p.).

Seri
Sciences. IMAGE. Imagery in life sciences

Genel Not
6.5. Computational-based methods

İçerik
Cover -- Title Page -- Copyright Page -- Contents -- Untitled -- Preface -- Chapter 1. Principles of Light Microscopy -- 1.1. Introduction -- 1.2. Principle of image formation -- 1.2.1. Geometric approach -- 1.2.2. Wave approach -- 1.2.3. Image formation under coherent light -- 1.2.4. Microscope resolution (diffraction-limited) -- 1.2.5. Abbe's theory of image formation -- 1.3. Optical sectioning techniques in fluorescence microscopy -- 1.3.1. Wide-field techniques -- 1.3.2. Point-scanning techniques -- 1.4. Conclusion -- 1.5. References
 
Chapter 2. Contrast-based Label-Free Imaging and Phase Measurement -- 2.1. Introduction, the biological object as an index object -- 2.2. Zernike phase contrast -- 2.2.1. Practical application and limitations -- 2.3. Differential interference contrast -- 2.3.1. Practical application and limitations -- 2.4. Other contrast methods with transparent objects -- 2.5. Measuring phase quantitatively: more than just contrast -- 2.6. Conclusions -- 2.7. References -- Chapter 3. Fluorophores and Labeling Methods for Fluorescence Microscopy -- 3.1. Introduction -- 3.2. Basics of fluorophore photophysics
 
3.3. Fluorescent proteins -- 3.4. Organic dyes -- 3.5. Conclusion -- 3.6. References -- Chapter 4. Quantitative FRAP and FCS -- 4.1. Life is motion -- 4.2. FRAP -- 4.2.1. Basics of FRAP -- 4.2.2. Quantitative principles of single spot FRAP -- 4.2.3. Analytical expression for principal origins of fluorescence recoveries -- 4.2.4. Variable radii FRAP -- 4.2.5. Quantitative imaging FRAP -- 4.2.6. Fluorescence loss in photobleaching -- 4.2.7. Photoactivation/photoconversion -- 4.3. FCS -- 4.3.1. Basic principle of correlation spectroscopy -- 4.3.2. Mathematics of FCS
 
4.3.3. Analytical expression for different origins of concentration fluctuations -- 4.3.4. Space and time correlation spectroscopy -- 4.4. Conclusion -- 4.5. References -- Chapter 5. Single-Particle Tracking for Nanoscale Dynamics of Biological Samples -- 5.1. Introduction -- 5.2. Nanoscale localization -- 5.3.Trajectory reconstruction -- 5.4. Nanoscale dynamics -- 5.4.1. Basic properties of Brownian motion -- 5.4.2. Quantification of experimental trajectories -- 5.4.3. Time-variable diffusion -- 5.4.4. Beyond Brownian motion: anomalous diffusion -- 5.5. References
 
Chapter 6. In Depth Microscopy -- 6.1. Introduction -- 6.2. Confocal microscopy -- 6.2.1. Principle -- 6.2.2. Spinning disk confocal microscopy -- 6.2.3. Limitations -- 6.2.4. Photon reassignment approaches -- the new confocal systems -- 6.3. Multi-photon microscopy -- 6.3.1. Principle -- 6.3.2. Laser-scanning multi-photon microscopy optical setup -- 6.3.3. Widefield multi-photon microscopy by temporal focusing -- 6.4. Light-sheet fluorescence microscopy -- 6.4.1. Principles and advantages -- 6.4.2. Light-sheet creation and properties -- 6.4.3. Main implementation overview

Özet
Light microscopy is a central tool in biological research, allowing scientists to observe living cells and organisms with details invisible to the naked eye.Since its inception in the 17th century, it has evolved through key innovations in optics, staining, electronics and informatics.

Notlar
John Wiley and Sons

Konu Terimleri
Microscopy -- Technique.
 
Microscopy -- Technological innovations.
 
Fluorescence microscopy.
 
Microscopie -- Technique.
 
Microscopie -- Innovations.
 
Microscopie de fluorescence.
 
Microscopes & Microscopy.
 
Biology.
 
Life Sciences.
 
SCIENCE.

Tür
Electronic books.

Yazar Ek Girişi
Sibarita, Jean-Baptiste,

Elektronik Erişim
https://onlinelibrary.wiley.com/doi/book/10.1002/9781394417896


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