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dc.contributor.authorEskandari, L
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorZarghami, N
dc.contributor.authorRahmati-Yamchi, M
dc.date.accessioned2018-08-26T05:39:07Z
dc.date.available2018-08-26T05:39:07Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/40150
dc.description.abstractIn breast cancer, a proper biomarker for the assessment of metastasis and poor prognosis is the RNA of activated leukocyte cell adhesion molecule (ALCAM) gene, which is expressed at high levels in breast tumor. We applied DNA-functionalized gold nanoparticles as the target-specific probes, for detecting specific sequences of DNA or RNA. At high MgCL2 concentrations, nanoprobes aggregate in the absence of the complementary DNA sequence and alteration in the solution color is detectable by evaluating the localized surface plasmon resonance (LSPR). But in the presence of complementary DNA, nanoprobes hybridize to the complementary sequence; therefore, no aggregation takes place, and no color change is observed. We designed a gold nanoprobe-based method that promptly detects the ALCAM gene expression in a low reaction volume with high sensitivity and specificity. This method is simple, fast, selective, and quantitative and can be done with small concentrations of the target (fmol/?L). Limit of detection of the method corresponded to 300?fmol/?L of synthetic ALCAM target.
dc.language.isoEnglish
dc.relation.ispartofArtificial cells, nanomedicine, and biotechnology
dc.subjectAntigens, CD
dc.subjectBiomarkers, Tumor
dc.subjectBiosensing Techniques
dc.subjectBreast Neoplasms
dc.subjectCell Adhesion Molecules, Neuronal
dc.subjectCell Line, Tumor
dc.subjectFemale
dc.subjectFetal Proteins
dc.subjectGold
dc.subjectHumans
dc.subjectMetal Nanoparticles
dc.subjectNeoplasm Proteins
dc.subjectSensitivity and Specificity
dc.titleGold nanoprobe-based method for sensing activated leukocyte cell adhesion molecule (ALCAM) gene expression, as a breast cancer biomarker.
dc.typearticle
dc.citation.volume45
dc.citation.issue2
dc.citation.spage277
dc.citation.epage282
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.3109/21691401.2016.1146732


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