
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
Tür:
Yazar Ek Girişi:
Elektronik Erişim:
https://onlinelibrary.wiley.com/doi/book/10.1002/9781394417896Kopya:
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Kütüphane | Materyal Türü | Demirbaş Numarası | Yer Numarası | Durumu/İade Tarihi | Materyal Ayırtma |
|---|---|---|---|---|---|
Arıyor... | E-Kitap | 600226-1001 | QH205.2 .S53 2025 | Arıyor... | Arıyor... |
