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
Link To Document :
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