Influence of different buffers (HEPES/MOPS) on keratinocyte cell viability and microbial growth

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:02:16Z
dc.date.available2018-12-11T17:02:16Z
dc.date.created2018-12-11T17:02:16Z
dc.date.issued2016-06-01
dc.identifierJournal of Microbiological Methods, v. 125, p. 40-42.
dc.identifier1872-8359
dc.identifier0167-7012
dc.identifierhttp://hdl.handle.net/11449/172809
dc.identifier10.1016/j.mimet.2016.03.018
dc.identifier2-s2.0-84962921676
dc.identifier2-s2.0-84962921676.pdf
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.
dc.languageeng
dc.relationJournal of Microbiological Methods
dc.relation0,696
dc.rightsAcesso aberto
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 growth
dc.typeOtros


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