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首页> 外文期刊>Journal of biomedical nanotechnology >Bioconjugation of gold and silver nanoparticles synthesized by Fusarium oxysporum and their use in rapid identification of Candida species by using bioconjugate-nano-polymerase chain reaction
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Bioconjugation of gold and silver nanoparticles synthesized by Fusarium oxysporum and their use in rapid identification of Candida species by using bioconjugate-nano-polymerase chain reaction

机译:尖孢镰刀菌合成金和银纳米粒子的生物共轭及其在生物共轭-纳米聚合酶链反应中快速鉴定念珠菌的应用

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摘要

We developed a Bioconjugate-Nano-PCR as a rapid and specific method for identification of Candida species in less time. This requires very low concentration of master mix and DNA sample of Candida albicans in conjugation with gold nanoparticles (AuNPs) and silver nanoparticles (AgNPs). We report a modification of the PCR assay with nanoparticles that allows the detection of high fidelity amplification of ITS-rDNA and beta (β) tubulin gene of Candida species from low concentrated DNA in short period. We synthesized and characterized the covalently attached 34 nm (AuNPs) and 35 nm of (AgNPs) and conjugated with C. albicans DNA sample, which is used as a template for PCR. The use of this nanoparticle modified template improves the sensitivity and specificity of the traditional PCR assay with very low cycles which is very helpful in molecular diagnostics and therapeutics. It proves to be an effective method for identification of Candida species with low concentration of DNA. This type of PCR assay is useful for detection of target gene by enhancing the specificity of the target gene and is less time consuming.
机译:我们开发了一种生物缀合物-纳米PCR作为一种快速,特异性的方法,可以在更短的时间内鉴定出念珠菌。这要求与金纳米颗粒(AuNPs)和银纳米颗粒(AgNPs)结合的白色假丝酵母的母液和DNA样品的浓度非常低。我们报告了纳米颗粒PCR检测方法的改进,该方法可以在短时间内从低浓度DNA检测念珠菌属物种的ITS-rDNA和β(β)微管蛋白基因的高保真扩增。我们合成并表征了共价结合的34 nm(AuNPs)和35 nm(AgNPs),并与白色念珠菌DNA样品偶联,将其用作PCR模板。这种纳米粒子修饰模板的使用以非常低的周期提高了传统PCR分析的灵敏度和特异性,这对分子诊断和治疗非常有帮助。它被证明是鉴定低浓度DNA念珠菌的有效方法。这种类型的PCR分析可通过增强靶基因的特异性来检测靶基因,并且耗时少。

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