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Primer composition for loop-mediated isothermal amplification reaction for detecting Honeysuckle yellow vein virus, and use thereof

机译:用于检测金银花黄脉病毒的环介导等温扩增反应的引物组合物及其用途

摘要

PURPOSE: A primer composition for loop-mediated isothermal amplification reaction for quickly detecting honeysuckle yellow vein virus is provided to early detect the virus, and to establish a quick and efficient system for diagnosing the virus. CONSTITUTION: A primer set for loop-mediated isothermal amplification reaction for detecting honeysuckle yellow vein virus contains sequence numbers 1-4. The virus is selected from the group consisting of Korea mutant strains(GQ477135), Japanese mutant strains(AB236325), New Zealand mutant strains(FJ817425), UK1 mutant strains(NC_005807), and UK2 mutant strains(AJ543429). A primer composition for loop-mediated isothermal amplification reaction for detecting honeysuckle yellow vein virus contains the primer set. The composition further contains DNA polymerase, dNTPs, and a reaction buffer. A method for detecting honeysuckle yellow vein virus comprises: a step of isolating genome DNAs; a step of performing loop-mediated isothermal amplification reaction at 60-70 deg. C for 30 minutes-2 hours; and a step of detecting the amplified product.
机译:目的:提供用于快速检测金银花黄脉病毒的环介导的等温扩增反应的引物组合物,以及早发现病毒,并建立快速有效的病毒诊断系统。组成:用于检测金银花黄脉病毒的环介导的等温扩增反应的引物组,其序列号为1-4。该病毒选自韩国突变株(GQ477135),日本突变株(AB236325),新西兰突变株(FJ817425),UK1突变株(NC_005807)和UK2突变株(AJ543429)。用于检测金银花黄脉病毒的环介导的等温扩增反应的引物组合物包含引物组。该组合物还包含DNA聚合酶,dNTP和反应缓冲液。一种金银花黄脉病毒的检测方法,包括:分离基因组DNA的步骤;在60-70℃下进行环介导的等温扩增反应的步骤。 C 30分钟至2小时;检测扩增产物的步骤。

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