Abstract
Confocal microscopy is routinely used to produce high-resolution images of single, double-, and triple labeled fluorescent samples. The images are collected as single optical sections (2D imaging), as Z-series (3D imaging), as time-lapse series (2D over time), or as Z-series over time (3D over time or 4D imaging). Because the images are in a digital format, they can be further manipulated using a range of software.
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© 1999 Humana Press Inc., Totowa, NJ
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Halder, G., Paddock, S.W. (1999). Presentation of Confocal Images. In: Paddock, S.W. (eds) Confocal Microscopy Methods and Protocols. Methods in Molecular Biology™, vol 122. Humana Press. https://doi.org/10.1385/1-59259-722-X:373
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DOI: https://doi.org/10.1385/1-59259-722-X:373
Publisher Name: Humana Press
Print ISBN: 978-0-89603-526-3
Online ISBN: 978-1-59259-722-2
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