Unit

UNIT 2.1 Fluorescence Microscopy: A Concise Guide to Current Imaging Methods

  1. Christian A. Combs

Published Online: 1 JAN 2010

DOI: 10.1002/0471142301.ns0201s50

Current Protocols in Neuroscience

Current Protocols in Neuroscience

How to Cite

Combs, C. A. 2010. Fluorescence Microscopy: A Concise Guide to Current Imaging Methods. Current Protocols in Neuroscience. 50:2.1:2.1.1–2.1.14.

Author Information

  1. NHLBI Light Microscopy Facility, NIH, Bethesda, Maryland

Publication History

  1. Published Online: 1 JAN 2010
  2. Published Print: JAN 2010

Abstract

The field of fluorescence microscopy is rapidly growing, providing ever increasing imaging capabilities for cell and neurobiologists. Over the last decade, many new technologies and techniques have been developed which allow for deeper, faster, or higher resolution imaging. For the non-expert microscopist, it can be difficult to match the best imaging technique to the biological question to be examined. Picking the right technique requires a basic understanding of the underlying imaging physics for each technique, as well as an informed comparison and balancing of competing imaging properties in the context of the sample to be imaged. This unit provides concise descriptions of a range of commercially available imaging techniques and provides a tabular guide to choosing among them. Techniques covered include structured light, confocal, total internal reflection fluorescence (TIRF), two-photon, and stimulated emission depletion (STED) microscopy. Curr. Protoc. Neurosci. 50:2.1.1-2.1.14. © 2010 by John Wiley & Sons, Inc.

Keywords:

  • confocal;
  • two-photon;
  • structured light;
  • STED