The Histochemical Journal

, Volume 26, Issue 9, pp 687–694

Deconvolution in 3-D optical microscopy

  • Peter Shaw

DOI: 10.1007/BF00158201

Cite this article as:
Shaw, P. Histochem J (1994) 26: 687. doi:10.1007/BF00158201


Fluorescent probes are becoming ever more widely used in the study of subcellular structure, and determination of their three-dimensional distributions has become very important. Confocal microscopy is now a common technique for overcoming the problem of out-of-focus flare in fluorescence imaging, but an alternative method uses digital image processing of conventional fluorescence images — a technique often termed ‘deconvolution’ or ‘restoration’. This review attempts to explain image deconvolution in a non-technical manner. It is also applicable to 3-D confocal images, and can provide a further significant improvement in clarity and interpretability of such images. Some examples of the application of image deconvolution to both conventional and confocal fluorescence images are shown.

Copyright information

© Chapman & Hall 1994

Authors and Affiliations

  • Peter Shaw
    • 1
  1. 1.Department of Cell BiologyJohn Innes CentreNorwichUK