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dc.contributor.authorGonzález González, María
dc.contributor.authorBartolome, Raquel
dc.contributor.authorJara-Acevedo, Ricardo
dc.contributor.authorCasado-Vela, Juan
dc.contributor.authorDasilva Freire, Noelia 
dc.contributor.authorMatarraz Sudón, Sergio 
dc.contributor.authorGarcía García, Jacinto 
dc.contributor.authorAlcázar Montero, José Antonio 
dc.contributor.authorSayagués Manzano, José María 
dc.contributor.authorOrfao de Matos Correia e Vale, José Alberto 
dc.contributor.authorFuentes García, Manuel 
dc.contributor.authorDasilva, Noelia
dc.contributor.authorMatarraz, Sergio
dc.contributor.authorGarcía García, Jacinto 
dc.contributor.authorAlcázar Montero, José Antonio 
dc.contributor.authorOrfao de Matos Correia e Vale, José Alberto 
dc.contributor.authorFuentes, Manuel
dc.date.accessioned2024-12-02T17:47:04Z
dc.date.available2024-12-02T17:47:04Z
dc.date.issued2014
dc.identifier.citationGonzález-González, M., Bartolome, R., Jara-Acevedo, R., Casado-Vela, J., Dasilva, N., Matarraz, S., García, J., Alcazar, J. A., Sayagues, J. M., Orfao, A., y Fuentes, M. (2014). Evaluation of homo- and hetero-functionally activated glass surfaces for optimized antibody arrays. Analytical Biochemistry, 450, 37-45. https://doi.org/10.1016/j.ab.2014.01.002es_ES
dc.identifier.issn0003-2697
dc.identifier.issn1096-0309
dc.identifier.urihttp://hdl.handle.net/10366/160887
dc.description.abstract[EN]Antibody arrays hold great promise for biomedical applications, but they are typically manufactured using chemically functionalized surfaces that still require optimization. Here, we describe novel hetero-functionally activated glass surfaces favoring oriented antibody binding for improved performance in protein microarray applications. Antibody arrays manufactured in our facility using the functionalization chemistries described here proved to be reproducible and stable and also showed good signal intensities. As a proof-of-principle of the glass surface functionalization protocols described in this article, we built antibody-based arrays functionalized with different chemistries that enabled the simultaneous detection of 71 human leukocyte membrane differentiation antigens commonly found in peripheral blood mononuclear cells. Such detection is specific and semi-quantitative and can be performed in a single assay under native conditions. In summary, the protocol described here, based on the use of antibody array technology, enabled the concurrent detection of a set of membrane proteins under native conditions in a specific, selective, and semi-quantitative manner and in a single assay.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntibody arrayses_ES
dc.subjectSurface functionalizationes_ES
dc.subjectAntibody immobilizationes_ES
dc.subjectProtein microarrayses_ES
dc.subjectFunctionalized surfaceses_ES
dc.titleEvaluation of homo- and hetero-functionally activated glass surfaces for optimized antibody arrayses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://www.sciencedirect.com/science/article/pii/S0003269714000141es_ES
dc.subject.unesco2211.28 Superficies
dc.subject.unesco2412.02 Anticuerpos
dc.identifier.doi10.1016/j.ab.2014.01.002
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleAnalytical Biochemistryes_ES
dc.volume.number450es_ES
dc.page.initial37es_ES
dc.page.final45es_ES
dc.type.hasVersioninfo:eu-repo/semantics/draftes_ES


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