Two-Photon STED Microscopy for Nanoscale Imaging of Neural Morphology In Vivo

The advent of super-resolution microscopy offers to bridge the gap between electron and light microscopy. It has opened up the possibility of visualizing cellular structures and dynamic signaling events on the "mesoscale" well below the classic diffraction barrier of light microscopy (10-2...

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Bibliographic Details
Published in:	Methods in molecular biology (Clifton, N.J.) Vol. 1663; p. 45
Main Authors:	Ter Veer, Mirelle J T, Pfeiffer, Thomas, Nägerl, U Valentin
Format:	Journal Article
Language:	English
Published:	United States 01.01.2017
Subjects:	Animals Dendritic Spines Mice Microglia - cytology Microscopy, Fluorescence - instrumentation Microscopy, Fluorescence - methods Nanotechnology Neurons - cytology Cranial window Nanoscale neural morphology Dendritic spines Microglia-synapse interactions Microglial processes Acute brain slice s Two-photon microscopy Mouse cortex STED microscopy Super-resolution imaging in vivo
ISSN:	1940-6029, 1940-6029
Online Access:	Get more information
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