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dc.contributor.authorAlonso Alonso, María Teresa 
dc.contributor.authorRodríguez Prados, Macarena
dc.contributor.authorNavas Navarro, Paloma
dc.contributor.authorRojo Ruiz, Jonathan
dc.contributor.authorGarcía-Sancho Martín, Francisco Javier 
dc.date.accessioned2019-03-22T11:22:18Z
dc.date.available2019-03-22T11:22:18Z
dc.date.issued2017
dc.identifier.citationCell Calcium Volume 64, 2017, Pages 3-11es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/35194
dc.descriptionProducción Científicaes
dc.description.abstractAequorins are excellent tools for measuring intra-organellar Ca2+ and assessing its role in physiological and pathological functions. Here we review targeting strategies to express aequorins in various organelles. We address critical topics such as probe affinity tuning as well as normalization and calibration of the signal. We also focus on bioluminescent Ca2+ imaging in nucleus or mitochondria of living cells. Finally, recent advances with a new chimeric GFP-aequorin protein (GAP), which can be used either as luminescent or fluorescent Ca2+ probe, are presented. GAP is robustly expressed in transgenic flies and mice, where it has proven to be a suitable Ca2+ indicator for monitoring physiological Ca2+ signaling ex vivo and in vivo.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleUsing aequorin probes to measure Ca2+ in intracellular organelleses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1016/j.ceca.2017.01.006es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0143416016302263es
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía, Industria y Competitividad (Project BFU2014-53469P)es
dc.description.projectInstituto de Salud Carlos III (TerCel, RD16/0011/0003)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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