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dc.contributor.authorHernández-Ortego, Pabloes_ES
dc.contributor.authorTorres-Montero, Remedioses_ES
dc.contributor.authorPeña, Elvira de laes_ES
dc.contributor.authorViana, Félixes_ES
dc.contributor.authorFernández-Trillo, Jorgees_ES
dc.date.accessioned2023-03-27T18:33:29Z-
dc.date.available2023-03-27T18:33:29Z-
dc.date.issued2022-12-18-
dc.identifier.citationInternational Journal of Molecular Sciences 23(24): 16164 (2022)es_ES
dc.identifier.issn1661-6596-
dc.identifier.urihttp://hdl.handle.net/10261/304491-
dc.descriptionThis article belongs to the Special Issue Targeting TRP Channels for Pain, Itch and Inflammation Relief.es_ES
dc.description.abstractTRPM8 is a non-selective cation channel expressed in primary sensory neurons and other tissues, including the prostate and urothelium. Its participation in different physiological and pathological processes such as thermoregulation, pain, itch, inflammation and cancer has been widely described, making it a promising target for therapeutic approaches. The detection and quantification of TRPM8 seems crucial for advancing the knowledge of the mechanisms underlying its role in these pathophysiological conditions. Antibody-based techniques are commonly used for protein detection and quantification, although their performance with many ion channels, including TRPM8, is suboptimal. Thus, the search for reliable antibodies is of utmost importance. In this study, we characterized the performance of six TRPM8 commercial antibodies in three immunodetection techniques: Western blot, immunocytochemistry and immunohistochemistry. Different outcomes were obtained for the tested antibodies; two of them proved to be successful in detecting TRPM8 in the three approaches while, in the conditions tested, the other four were acceptable only for specific techniques. Considering our results, we offer some insight into the usefulness of these antibodies for the detection of TRPM8 depending on the methodology of choice.es_ES
dc.description.sponsorshipDuring the course of this work, PH was supported by an FPI predoctoral fellowship (BES-2017-080782). This study was funded by MICIN/AEI/10.13039/501100011033 (PID2019-108194RB-I00), Generalitat Valenciana (PROMETEO/2021/031) and the Severo Ochoa Programme for Centres of Excellence in R&D (ref. SEV-2017-0723).es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institutees_ES
dc.relationinfo:eu-repo/grantAgreement/AEI//BES-2017-080782es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108194RB-I00/ES/DIVERSIDAD MOLECULAR Y CELULAR DE LOS RECEPTORES TERMICOS Y MECANICOS: PAPEL EN LOS MECANISMOS PERIFERICOS Y CENTRALES DEL DOLOR CRONICO/es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI//SEV-2017-0723es_ES
dc.relation.ispartofInternational journal of molecular scienceses_ES
dc.relation.isversionofPublisher's versiones_ES
dc.relation.isbasedonThe underlying dataset has been published as supplementary material of the article in the publisher platform at DOI 10.3390/ijms232416164-
dc.rightsopenAccesses_ES
dc.subjectTRPM8es_ES
dc.subjectWestern blotes_ES
dc.subjectImmunocytochemistryes_ES
dc.subjectImmunohistochemistryes_ES
dc.titleValidation of six commercial antibodies for the detection of heterologous and endogenous TRPM8 ion channel expressiones_ES
dc.typeartículoes_ES
dc.identifier.doi10.3390/ijms232416164-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/ijms232416164es_ES
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)es_ES
dc.contributor.funderAgencia Estatal de Investigación (España)es_ES
dc.contributor.funderGeneralitat Valencianaes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003359es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011033es_ES
dc.contributor.orcidViana, Félix [0000-0003-1439-949X]es_ES
dc.identifier.pmid36555804-
dc.identifier.scopus2-s2.0-85144557223-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85144557223-
dc.subject.urihttp://metadata.un.org/sdg/3es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
dc.subject.sdgEnsure healthy lives and promote well-being for all at all ageses_ES
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeartículo-
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