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dc.contributor.authorDurisic, Nela
dc.contributor.authorLaparra Cuervo, Lara
dc.contributor.authorLakadamyali, Melike
dc.contributor.otherUniversitat Politècnica de Catalunya. Institut de Ciències Fotòniques
dc.date.accessioned2016-07-19T08:16:58Z
dc.date.available2016-07-19T08:16:58Z
dc.date.issued2014-06-01
dc.identifier.issn1367-5931
dc.identifier.urihttp://hdl.handle.net/2117/88879
dc.description.abstractSuper-resolution microscopy is an enabling technology that allows biologists to visualize cellular structures at nanometer length scales using far-field optics. To break the diffraction barrier, it is necessary to leverage the distinct molecular states of fluorescent probes. At the same time, the existence of these different molecular states and the photophysical properties of the fluorescent probes can complicate data quantification and interpretation. Here, we review the pitfalls in super-resolution data analysis that must be avoided for proper interpretation of images.
dc.format.extent7 p.
dc.language.isoeng
dc.publisherScienceDirect
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Física
dc.subject.lcshmicroscopy
dc.subject.othermicroscopy
dc.titleQuantitative super-resolution microscopy: pitfalls and strategies for image analysis
dc.typeArticle
dc.subject.lemacMicroscòpia
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttp://doi.org/10.1016/j.cbpa.2014.04.005
dc.rights.accessOpen Access
dc.description.versionPostprint (author's final draft)
dc.relation.projectidinfo:eu-repo/grantAgreement/EC/FP7/337191/EU/On the move: Motor-cargo and motor-microtubule interactions studied with quantitative, high spatio-temporal resolution microscopy in vivo/MOTORS
local.citation.pubplaceUSA
local.citation.publicationNameCurrent Opinion in Chemical Biology
local.citation.volume20
local.citation.startingPage22
local.citation.endingPage28
local.personalitzacitaciotrue


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