dc.creatorEggeling, Christian
dc.creatorWillig, Katrin I.
dc.creatorBarrantes, Francisco José
dc.date.accessioned2019-09-17T18:39:19Z
dc.date.accessioned2022-09-29T16:29:44Z
dc.date.available2019-09-17T18:39:19Z
dc.date.available2022-09-29T16:29:44Z
dc.date.created2019-09-17T18:39:19Z
dc.date.issued2013
dc.identifierEggeling C, Willig KI, Barrantes FJ. STED microscopy of living cells – new frontiers in membrane and neurobiology. Journal of Neurochemistry. 2013;126(2):203-212. doi:10.1111/jnc.12243. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/8754
dc.identifierhttps://repositorio.uca.edu.ar/handle/123456789/8754
dc.identifier10.1111/jnc.12243
dc.identifier23506404
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3789420
dc.description.abstractAbstract: Recent 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.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsAcceso abierto
dc.sourceJournal of Neurochemistry Vol. 126, N° 2, 2013
dc.subjectNEUROBIOLOGIA
dc.subjectMICROSCOPIA
dc.subjectNANOTECNOLOGIA
dc.subjectIMAGENES DE FLUORESCENCIA
dc.subjectMEMBRANA PLASMATICA
dc.titleSTED microscopy of living cells--new frontiers in membrane and neurobiology
dc.typeArtículos de revistas


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