Genotyping Interleukin-10 High and Low Producers with Single-Tube Bidirectional Allele-Specific Amplification

J. Karhukorpi, R. Karttunen
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引用次数: 18

Abstract

A simple bidirectional allele-specific PCR method is described for determining the -1082 A and G alleles in the interleukin-10 (IL-10) promoter region. This polymorphism is associated with IL-10 production capacity, and it is thus interesting to see whether different infectious and autoimmune conditions are associated with it. With our method, the A and G alleles may be studied simultaneously in a single PCR reaction, as amplification of the different alleles is performed by using 3′-mismatched and partly overlapping allele-specific upstream and downstream primers around the -1082 site. The fast and simple method described here is especially suitable for large-scale association studies.
用单管双向等位基因特异性扩增法分型白细胞介素-10高、低生产者
描述了一种简单的双向等位基因特异性PCR方法,用于测定白细胞介素-10 (IL-10)启动子区域的-1082 A和G等位基因。这种多态性与IL-10的生产能力有关,因此观察不同的感染和自身免疫性疾病是否与之相关是很有趣的。利用我们的方法,可以在一个PCR反应中同时研究A和G等位基因,因为不同等位基因的扩增是通过在-1082位点附近使用3 '错配和部分重叠的等位基因特异性上游和下游引物进行的。这里描述的快速和简单的方法特别适合于大规模的关联研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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