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Different contribution of carbon nanotubes and graphene oxide in single nucleotide polymorphism for the diagnosis of human mad-cow disease

机译:碳纳米管和氧化石墨烯在单核苷酸多态性对人疯牛病诊断中的不同贡献

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Rapid single nucleotide polymorphism (SNP) with 1,1'-oxalylimidazole chemiluminescence (ODI-CL) detection was developed for the early diagnosis of human mad-cow disease. Mutated single strand DNA (ssDNA) sequence discovered from patients having human mad-cow disease rapidly hybridize with complementary probe conjugated with chemiluminescent dye. The hybridization between target ssDNA and complementary probe was dependent on four different variables such as pH, temperature, incubation time, and the type of nanoparticles (e.g., multi-walled carbon nanotubes, graphene oxide) capable of capturing mismatched ssDNAs and excess complementary probe. However, three different types of mismatched ssDNAs also slowly hybridize with complementary probe with the increase of incubation time. The problem was solved by using ODI-CL detection instead of fluorescence detection of conventional SNP because ODI-CL is about 100 times more sensitive than fluorescence. In other words, it was possible to reduce the interaction between mismatched ssDNAs and complementary probe with short incubation time (15 minutes) using highly sensitive ODI-CL detection. Based on the results, in conclusion, it is expected that SNP with ODI-CL can be applied as a cost-effective, rapid, and simple analytical method to diagnose and prognose various diseases.
机译:具有1,1'-氧杂咪唑化学发光(ODI-CL)检测的快速单核苷酸多态性(SNP)被开发用于人类疯牛病的早期诊断。从患有人疯牛病的患者中发现的突变单链DNA(ssDNA)序列与与化学发光染料偶联的互补探针快速杂交。目标ssDNA与互补探针之间的杂交取决于四个不同的变量,例如pH,温度,孵育时间以及能够捕获错配的ssDNA和过量互补探针的纳米颗粒的类型(例如多壁碳纳米管,氧化石墨烯)。然而,随着温育时间的增加,三种不同类型的错配的ssDNA也与互补探针缓慢杂交。通过使用ODI-CL检测代替常规SNP的荧光检测解决了该问题,因为ODI-CL的灵敏度比荧光高约100倍。换句话说,使用高灵敏度的ODI-CL检测,可以在较短的孵育时间(15分钟)内减少错配的ssDNA与互补探针之间的相互作用。综上所述,基于这些结果,可以预期的是,带有ODI-CL的SNP可以作为一种经济有效,快速,简单的分析方法来诊断和预后各种疾病。

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