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A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application

机译:一种用于检测ACE基因插入/缺失多态性的新型PCR方法及其临床应用

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Abstract Background Angiotensin-converting enzyme (ACE) plays a major role in blood pressure regulation and cardiovascular homeostasis. The wide distribution and multifunctional properties of ACE suggest it’s involvement in various pathophysiological conditions. Results In this study, a novel visual detection method for ACE I/D polymorphisms was designed by integrating direct PCR without the need for DNA extraction using gold magnetic nanoparticles (GMNPs)-based lateral flow assay (LFA) biosensor. The entire detection procedure could enable the genotyping of clinical samples in about 80?min. The detection limit was 0.75?ng and results could be obtained in 5?min using the LFA device. Three hundred peripheral blood samples were analyzed using the direct PCR-LFA system and then verified by sequencing to determine accuracy and repeatability. A clinical preliminary study was then performed to analyze a total of 633 clinical samples. Conclusions After grouping based on age, we found a significant difference between the genotypes and the age of patients in the CHD group. The introduction of this method into clinical practice may be helpful for the diagnosis of diseases caused by large fragment gene insertions/deletions.
机译:摘要背景血管紧张素转换酶(ACE)在血压调节和心血管稳态中起着重要作用。 ACE的广泛分布和多功能特性表明它参与了各种病理生理病症。结果在本研究中,通过使用Gold磁性纳米颗粒(GMNP)基于横向流动测定(LFA)生物传感器,通过整合直接PCR来设计一种新的视觉检测方法。整个检测程序可以使临床样品的基因分型在约80?min中。检测限为0.75≤NG,并且可以使用LFA器件在5·min中获得结果。使用直接PCR-LFA系统分析三百个外周血样品,然后通过测序验证以确定精度和可重复性。然后进行临床初步研究以分析总共633个临床样品。基于年龄进行分组后结论,我们发现了CHD组的基因型和患者年龄之间存在显着差异。这种方法引入临床实践可能有助于诊断由大片段基因插入/缺失引起的疾病。

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