首页> 外文期刊>American journal of molecular biology >Specificity of Various Mitochondrial DNA (&i&mt&/i&DNA), &i&ND5&/i&, &i&D-Loop&/i&, and &i&Cty-b&/i& DNA Primers in Detecting Pig (&i&Sus scrofa&/i&) DNA Fragments
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Specificity of Various Mitochondrial DNA (&i&mt&/i&DNA), &i&ND5&/i&, &i&D-Loop&/i&, and &i&Cty-b&/i& DNA Primers in Detecting Pig (&i&Sus scrofa&/i&) DNA Fragments

机译:各种线粒体DNA的特异性(小于I> MT< / I> DNA),LT; I> ND5< / I&中< I> d - 环LT; I&GT /;和& I> CTY-b将/我& DNA引物检测猪(& i& sus scrofa& / i&)DNA片段

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摘要

Polymerase Chain Reaction (PCR) is an accurate, simple and fast analytical method. This technique is widely used in the identification of meat adulteration and meat-based processed food products. Three Mitochondrial DNA (mt-DNA) primers NADH Dehydrogenase sub unit 5 ( ND5 ), D-Loop , and Cytochrome b ( Cyt-b ) were tested for their specificity in detecting of pig ( Sus scrofa ) DNA fragments. DNA genome from 6 meat samples (pork, beef, goat, lamb, and chicken) was amplified by PCR technique using three pairs of primers ( ND5, D-Loop , and Cyt-b ) and sequenced. The results of amplification using the three primers produced specific DNA bands with the lengths of 232 bp, 951 bp, and 404 bp, respectively. Comparison results with ND5, D-Loop, and Cyt-b gene sequences resulted in similarity values of 100%, 97%, and 99%, respectively. These showed that the mt-DNA primers of ND5, D-Loop , and Cyt-b genes can be recommended as specific primers in detecting pig ( Sus scrofa ) DNA fragments.
机译:聚合酶链反应(PCR)是一种准确,简单,快速的分析方法。该技术广泛用于识别肉掺假和肉类加工食品。测试了三种线粒体DNA(MT-DNA)引物NADH脱氢酶子单元5(ND5),D圈和细胞色素B(CYT-B)以检测猪(SUS scrofa)DNA片段的特异性。通过使用三对引物(ND5,D环和CYT-B)并测序PCR技术,通过PCR技术扩增来自6种肉样品(猪肉,牛肉,山羊,羊肉)和测序的DNA基因组。使用三个引物的扩增结果分别产生具有232bp,951bp和404bp的长度的特异性DNA带。 ND5,D环和CYT-B基因序列的比较结果分别导致相似性为100%,97%和99%。这些显示,可以推荐ND5,D环和CYT-B基因的MT-DNA引物作为检测猪(SUS Scrofa)DNA片段中的特异性引物。

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