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首页> 外文期刊>Journal of Bioinformatics and Sequence Analysis >Primer designing for PreS region of hepatitis B virus from the most conserved patches of hepatitis B virus genome
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Primer designing for PreS region of hepatitis B virus from the most conserved patches of hepatitis B virus genome

机译:从最保守的乙型肝炎病毒基因组补丁设计用于乙型肝炎病毒PreS区域的引物设计

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摘要

The most conserved regions for 15 hepatitis B virus complete genome of different subtypes were aligned using PCGENE software CLUSTAL to design a new pair of primer that can bind to each subtype of hepatitis B virus (HBV), to amplify PreS region of HBV genome. A pair of primer from these conserved patches was selected using software PRIMER and named as Nhepf1 and Nhepr1. Nhepf1, forward primer bound 2362-2385 nucleotides and Nhepr1, reverse primer bound 260-283 nucleotide amplify 1.12 Kb region of HBV genome that contain PreS sequence. The pair of primer was optimized for PCR. Nhepf1 and Nhepr1 annealed well at 50°C to subtype adw2 (American), adr4 (Japanese) and Pakistanian patient derived HBV DNA without any nonspecific bands. The results were found to be highly reproducible with greater accuracy.
机译:使用PCGENE软件CLUSTAL对15个不同亚型的乙型肝炎病毒完整基因组的最保守区域进行比对,以设计一对可以结合每种乙型肝炎病毒(HBV)亚型的新引物,以扩增HBV基因组的PreS区域。使用软件PRIMER从这些保守的补丁中选择一对引物,分别命名为Nhepf1和Nhepr1。 Nhepf1,正向引物结合了2362-2385个核苷酸,Nhepr1,反向引物结合了260-283个核苷酸,扩增了含有PreS序列的HBV基因组的1.12 Kb区。对引物对进行PCR优化。 Nhepf1和Nhepr1在50°C退火得很好,亚型adw2(美国),adr4(日本)和巴基斯坦患者衍生的HBV DNA没有任何非特异性条带。发现结果具有较高的重复性,并且准确性更高。

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