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Fb2 Confocal Microscopy And Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging (SPIE Press Monograph Vol. PM161) ePub

by Barry R. Masters

Category: Medicine and Health Sciences
Subcategory: Other
Author: Barry R. Masters
ISBN: 0819461180
ISBN13: 978-0819461186
Language: English
Publisher: SPIE Publications (February 9, 2006)
Pages: 230
Fb2 eBook: 1332 kb
ePub eBook: 1722 kb
Digital formats: lrf azw rtf lit

Date Published: 9 February 2006 Pages: 230 ISBN: 9780819461186 Volume: PM161. 1. In-Vivo Microscopy or Live Cell and Tissue Imaging. Instrument Development.

Confocal Microscopy and Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging. Author(s): Barry R. Masters. Date Published: 9 February 2006 Pages: 230 ISBN: 9780819461186 Volume: PM161.

On July 20, we had the largest server crash in the last 2 years This text guides you through the principles and practical techniques of confocal and multiphoton microscopy.

On July 20, we had the largest server crash in the last 2 years. This text guides you through the principles and practical techniques of confocal and multiphoton microscopy. It also describes the historical connections and parallel inventions that resulted in modern techniques of live cell imaging and their use in biology and medicine.

Confocal microscopy, most frequently confocal laser scanning microscopy (CLSM) or laser confocal scanning microscopy (LCSM), is an optical imaging technique for increasing optical resolution and contrast of a micrograph by means of using a spatial p. .

Confocal microscopy, most frequently confocal laser scanning microscopy (CLSM) or laser confocal scanning microscopy (LCSM), is an optical imaging technique for increasing optical resolution and contrast of a micrograph by means of using a spatial pinhole to block out-of-focus light in image formation. Capturing multiple two-dimensional images at different depths in a sample enables the reconstruction of three-dimensional structures (a process known as optical sectioning) within an object.

Home eBooks Confocal Microscopy and Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging Speculation on FutureĀ . SPIE books (print and digital) may be purchased individually on SPIE.

Home eBooks Confocal Microscopy and Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging Speculation on Future Directions for Confocal and Multiphoton Excitation Microscopy. Contact your librarian to recommend SPIE eBooks for your organization. Translator Disclaimer.

Goodreads helps you keep track of books you want to read. Published February 1st 2006 by SPIE-International Society for Optical Engineering. Start by marking Confocal Microscopy and Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging as Want to Read: Want to Read savin. ant to Read. Confocal Microscopy And Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging (SPIE Press Monograph Vol. PM161). 0819461180 (ISBN13: 9780819461186).

Confocal Microscopy and Multiphoton Excitation Microscopy : The Genesis of Live Cell Imaging.

This text guides you through the principles and practical techniques of confocal and multiphoton microscopy. You will find comparisons of different types of confocal and multiphoton microscopes, solutions to the problems one would encounter when using various microscopic techniques, tips on selecting equipment, and an extensive annotated bibliography of additional resources.

Two-photon excitation microscopy (TPEF or 2PEF) is a fluorescence imaging technique that allows imaging of living tissue up to about one millimeter in thickness. It differs from traditional fluorescence microscopy, in which the excitation wavelength. It differs from traditional fluorescence microscopy, in which the excitation wavelength is shorter than the emission wavelength, as the wavelengths of the two exciting photons are longer than the wavelength of the resulting emitted light.

Barry, R. Masters, Peter So, 2008.

Confocal Microscopy and Multiphoton Excitation Microscopy: The Genesis of Live Cell Imaging, SPIE Press Monograph, Vol. PM161, 2005. 5. Mertz, J. Introduction to Optical Microscopy, Roberts and Company Pu. 2010. 6. Barry, R. Handbook of Biomedical Nonlinear Optical Microscopy, Oxford University Press, 2008. Lippitz, . Erker, . Decker, . van Holde, . Basche, . Two-photon excitation microscopy of g proteins.

Confocal microscopy and multi-photon excitation microscopy of human skin in vivo. Department of Ophthalmology, University of Bern, Bern, 3010 Switzerland. 3. B. R. Masters, P. T. C. So, K. H. Kim, C. Buehler, and E. Gratton, Multiphoton excitation microscopy, confocal microscopy, and spectroscopy of living cells and tissues: functional metabolic imaging of human skin in vivo, in Methods in Enzymology, Confocal Microscopy, vol. 307, P. M. Conn, ed. (Academic Press, New York, 1999) Chap.

This text guides you through the principles and practical techniques of confocal and multiphoton microscopy. It also describes the historical connections and parallel inventions that resulted in modern techniques of live cell imaging and their use in biology and medicine. You will find comparisons of different types of confocal and multiphoton microscopes, solutions to the problems one would encounter when using various microscopic techniques, tips on selecting equipment, and an extensive annotated bibliography of additional resources.

Contents

- List of Abbreviations

- Preface

- Optical Microscopy

- Confocal Microscopy

- Nonlinear Microscopy

- The Path to Imaging Live Cells, Tissues, and Organs

- Epilogue

- Appendix: Reference Materials and Resources

- Index

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