17 August 1994 New waves in light microscopy
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Proceedings Volume 2137, Time-Resolved Laser Spectroscopy in Biochemistry IV; (1994); doi: 10.1117/12.182704
Event: OE/LASE '94, 1994, Los Angeles, CA, United States
Abstract
The light microscope is an icon of the sciences, but its sophistication and usefulness have had a far from linear evolution. During the last decade great progress in fluorescent probe design, light source and detector technology, and computers have contributed to a revolutionary increase in the capabilities of light microscopy, turning it from a static, 2D tool into a dynamic, 3D means of studying live biological specimens. We believe that the next wave in light microscopy is based on automation and improved spatio-temporal resolution. Our work on multimode robotic microscopy and standing wave-excited fluorescence microscopy is presented here. The former allows simultaneous imaging with several modes of light microscopy and good specimen control (temperature, displacement, chemistry), while the latter affords an axial resolution significantly improving on confocal microscopy and, for the first time, exceeding transverse resolution. Examples of biological information obtainable solely by these advances are also given.
© (1994) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Daniel L. Farkas, Brent Bailey, Frederick Lanni, D. Lansing Taylor, "New waves in light microscopy", Proc. SPIE 2137, Time-Resolved Laser Spectroscopy in Biochemistry IV, (17 August 1994); doi: 10.1117/12.182704; https://doi.org/10.1117/12.182704
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KEYWORDS
Microscopy

Microscopes

Luminescence

3D image processing

Image processing

Confocal microscopy

3D acquisition

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