Paper
10 May 1996 Two-photon excitation laser scanning microscopy: applications in neuroscience
Winfried Denk
Author Affiliations +
Abstract
High resolution fluorescence imaging in intact tissues faces special challenges posed by scattering of excitation and fluorescence light and the need to avoid photodynamic damage. Significant improvements over conventional widefield and confocal imaging are provided when two-photon excitation is used. Applications to the functional imaging of the calcium dynamics in synaptic spines, small invertebrate neurites, and auditory hair cells are shown. Two-photon absorption induced photolysis can also be used for scanning photochemical microscopy and for high resolution measurements of diffusional coupling between cellular compartments.
© (1996) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Winfried Denk "Two-photon excitation laser scanning microscopy: applications in neuroscience", Proc. SPIE 2678, Optical Diagnostics of Living Cells and Biofluids, (10 May 1996); https://doi.org/10.1117/12.239549
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KEYWORDS
Microscopy

Tissues

Spine

Confocal microscopy

Luminescence

Laser scanners

Light scattering

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