首页> 外文期刊>Journal of clinical laboratory analysis. >AT1 receptor A1166C and AT2 receptor -1332A/G gene polymorphisms: efficient genotyping by single-tube PCR.
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AT1 receptor A1166C and AT2 receptor -1332A/G gene polymorphisms: efficient genotyping by single-tube PCR.

机译:AT1受体A1166C和AT2受体-1332A / G基因多态性:通过单管PCR进行有效的基因分型。

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摘要

Angiotensin II type 1 receptor (AT1) and angiotensin II type 2 receptor (AT2) genes have been investigated in recent years as potential etiologic candidates for cardiovascular and renal diseases. The pathogenic implications of AT1 A1166C and AT2 A-1332G gene polymorphisms have been shown. Here we describe a rapid and reliable method for detecting both AT1 and AT2 gene polymorphisms by a single-tube PCR, to reduce analysis time and simplify the genotyping procedure. In contrast to previously described methods, our method does not require hybridization, primer extension, or nested PCR for genotyping. In most previous studies concerning gene polymorphisms of RAS, both AT1 and AT2 receptor gene polymorphisms were investigated. The advantage of our method is that it makes it possible to detect both of these polymorphisms in a duplex PCR. The procedure described is convenient for routine laboratory use with manual sample processing, and offers the potential for further automation as well. Its simplicity makes it practical for large-scale screening of individuals and families at risk for cardiovascular or renal diseases.
机译:近年来,已经研究了血管紧张素II 1型受体(AT1)和血管紧张素II 2型受体(AT2)基因作为心血管和肾脏疾病的潜在病因候选物。已经显示了AT1 A1166C和AT2 A-1332G基因多态性的致病意义。在这里,我们描述了一种通过单管PCR检测AT1和AT2基因多态性的快速而可靠的方法,以减少分析时间并简化基因分型过程。与先前描述的方法相比,我们的方法不需要杂交,引物延伸或巢式PCR进行基因分型。在大多数有关RAS基因多态性的研究中,都对AT1和AT2受体基因多态性进行了研究。我们方法的优点是可以在双重PCR中检测这两个多态性。所描述的程序对于常规实验室使用手动样品处理非常方便,并且还具有进一步自动化的潜力。它的简单性使其可用于大规模筛查有心血管或肾脏疾病风险的个人和家庭。

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