• Title of article

    Three-Dimensional Imaging by Deconvolution Microscopy

  • Author/Authors

    McNally، James G. نويسنده , , Karpova، Tatiana نويسنده , , Cooper، John نويسنده , , Conchello، José Angel نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1999
  • Pages
    -372
  • From page
    373
  • To page
    0
  • Abstract
    Deconvolution is a computational method used to reduce out-of-focus fluorescence in three-dimensional (3D) microscope images. It can be applied in principle to any type of microscope image but has most often been used to improve images from conventional fluorescence microscopes. Compared to other forms of 3D light microscopy, like confocal microscopy, the advantage of deconvolution microscopy is that it can be accomplished at very low light levels, thus enabling multiple focal-plane imaging of light-sensitive living specimens over long time periods. Here we discuss the principles of deconvolution microscopy, describe different computational approaches for deconvolution, and discuss interpretation of deconvolved images with a particular emphasis on what artifacts may arise.
  • Keywords
    interleukin-18 , cytokines , interferon GAMMA
  • Journal title
    METHODS : A COMPANION TO METHODS IN ENZYMOLOGY
  • Serial Year
    1999
  • Journal title
    METHODS : A COMPANION TO METHODS IN ENZYMOLOGY
  • Record number

    58119