STED microscopy of living cells: New frontiers in Membrane and Neurobiology

dc.creatorEggeling, Christian
dc.creatorWillig, Katrin I.
dc.creatorBarrantes, Francisco Jose
dc.date.accessioned2016-01-15T20:54:42Z
dc.date.accessioned2018-11-06T15:15:53Z
dc.date.available2016-01-15T20:54:42Z
dc.date.available2018-11-06T15:15:53Z
dc.date.created2016-01-15T20:54:42Z
dc.date.issued2013-04-23
dc.identifierEggeling, Christian; Willig, Katrin I.; Barrantes, Francisco Jose; STED microscopy of living cells: New frontiers in Membrane and Neurobiology; Wiley; Journal of Neurochemistry; 126; 2; 23-4-2013; 203-212
dc.identifier0022-3042
dc.identifierhttp://hdl.handle.net/11336/3661
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1895355
dc.description.abstractRecent developments in fluorescence far-field microscopy such as STED microscopy have accomplished observation of the living cell with a spatial resolution far below the diffraction limit. Here, we briefly review the current approaches to super-resolution optical microscopy and present the implementation of STED microscopy for novel insights into live cell mechanisms, with a focus on neurobiology and plasma membrane dynamics.
dc.languageeng
dc.publisherWiley
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1111/jnc.12243/abstract
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/DOI:10.1111/jnc.12243
dc.relationinfo:eu-repo/semantics/altIdentifier/issn/0022-3042
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectMICROSCOPY
dc.subjectSUPERRESOLUTION
dc.subjectSTED
dc.subjectNEUROSCIENCE
dc.titleSTED microscopy of living cells: New frontiers in Membrane and Neurobiology
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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