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Rapid and sensitive strategy for Human Papillomavirus (HPV) detection using a gene-based DNA nanobiosensor

机译:使用基于基于基于基于基于基因的DNA纳米血管传感器的人乳头瘤病毒(HPV)检测的快速和敏感策略

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Human Papillomavirus (HPV) is the most common sexually transmitted virus that infected to human. The most common high-risk HPV are 16 and 18. Most 70% of cervical cancers (CC) are due to infection by these genotypes. A rapid and sensitive strategy for the detection of Human Papillomavirus (HPV) was proposed by integrating simple DNA extraction with gene-based DNA nanobiosensor. DNA nanochip is a powerful tool allowing detection HPV target molecules present in a sample. The efficiency of DNA nanochip depends mainly on the sequence of the capture probes and the way they are attached to the support. The coupling procedure must be quick, covalent, and reproducible. The fabrication, immobilization and hybridization processes were characterized with current voltage (I-V) characterization (KEITHLEY, 6487). This strategy presented a simple, rapid and sensitive platform for HPV detection and would become a powerful tool for pathogenic microorganisms screening in clinical diagnosis.
机译:人乳头瘤病毒(HPV)是感染人类最常见的性传播病毒。 最常见的高风险HPV是16和18.大多数70%的宫颈癌(CC)是由于这些基因型的感染。 通过将简单的DNA萃取与基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于基于的DNA纳米来源传感器,提出了一种快速和敏感的策略。 DNA纳米是一种强大的工具,允许检测样品中存在的HPV靶分子。 DNA纳米普普的效率主要取决于捕获探针的序列和它们附着在载体上的方式。 耦合过程必须快速,共价和可重复。 具有电流电压(I-V)表征(Keithley,6487)的制造,固定化和杂交方法。 该策略提出了一种简单,快速敏感的HPV检测平台,并将成为临床诊断中致病微生物筛查的强大工具。

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