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dc.contributor.authorDias, Kássia de Carvalho [UNESP]
dc.contributor.authorBarbugli, Paula Aboud [UNESP]
dc.contributor.authorVergani, Carlos Eduardo [UNESP]
dc.date.accessioned2018-12-11T17:02:16Z
dc.date.available2018-12-11T17:02:16Z
dc.date.issued2016-06-01
dc.identifierhttp://dx.doi.org/10.1016/j.mimet.2016.03.018
dc.identifier.citationJournal of Microbiological Methods, v. 125, p. 40-42.
dc.identifier.issn1872-8359
dc.identifier.issn0167-7012
dc.identifier.urihttp://hdl.handle.net/11449/172809
dc.description.abstractThis study assessed the effect of the buffers 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) and 3-(N-morpholino) propanesulfonic acid (MOPS) on keratinocyte cell viability and microbial growth. It was observed that RPMI buffered with HEPES, supplemented with l-glutamine and sodium bicarbonate, can be used as a more suitable medium to promote co-culture.en
dc.format.extent40-42
dc.language.isoeng
dc.relation.ispartofJournal of Microbiological Methods
dc.sourceScopus
dc.subjectCandida albicans
dc.subjectCell survival
dc.subjectHEPES
dc.subjectKeratinocytes
dc.subjectStaphylococcus aureus
dc.titleInfluence of different buffers (HEPES/MOPS) on keratinocyte cell viability and microbial growthen
dc.typeNota
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Oral Rehabilitation Program-Araraquara School of Dentistry UNESP-Univ. Estadual Paulista Centro
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Oral Rehabilitation Program-Araraquara School of Dentistry UNESP-Univ. Estadual Paulista Centro
dc.identifier.doi10.1016/j.mimet.2016.03.018
dc.rights.accessRightsAcesso aberto
dc.identifier.scopus2-s2.0-84962921676
dc.identifier.file2-s2.0-84962921676.pdf
unesp.author.lattes3003130522427820[3]
unesp.author.orcid0000-0001-6476-020X[1]
unesp.author.orcid0000-0002-7375-4714[3]
dc.relation.ispartofsjr0,696
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