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Biophotonics pp 233-258 | Cite as

Microscopy

  • Gerd KeiserEmail author
Chapter
  • 2.4k Downloads
Part of the Graduate Texts in Physics book series (GTP)

Abstract

Many technical developments have appeared in recent years to enhance imaging performance and instrument versatility in optical microscopy for biophotonics and biomedical applications to visualize objects ranging in size from millimeters to nanometers. These developments include increasing the penetration depth in scattering media, improving image resolution beyond the diffraction limit, increasing image acquisition speed, enhancing instrument sensitivity, and developing better contrast mechanisms. This chapter first describes the basic concepts and principles of optical microscopy and then discusses the limitations of distinguishing two closely spaced points. Next, the functions of confocal microscopes, fluorescence microscopy, multiphoton microscopy, Raman microscopy, light sheet microscopy, and super-resolution fluorescence microscopy are given.

Keywords

Surface Enhance Raman Scattering Objective Lens Numerical Aperture Stimulate Raman Scattering Fluorescence Lifetime Imaging Microscopy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media Singapore 2016

Authors and Affiliations

  1. 1.Department of Electrical and Computer EngineeringBoston UniversityNewtonUSA

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