首页> 外国专利> NEW PRIMER PAIR FOR AMPLIFYING BETWEEN ITS REGIONS FROM 16SrRNA GENE OR 16SrRNA GENE OF POTATO SCAB-CAUSING STRAIN, AND METHOD FOR DETECTING AND IDENTIFYING POTATO SCAB-CAUSING STRAIN WITH THE NEW PRIMER PAIR

NEW PRIMER PAIR FOR AMPLIFYING BETWEEN ITS REGIONS FROM 16SrRNA GENE OR 16SrRNA GENE OF POTATO SCAB-CAUSING STRAIN, AND METHOD FOR DETECTING AND IDENTIFYING POTATO SCAB-CAUSING STRAIN WITH THE NEW PRIMER PAIR

机译:用于从马铃薯SC疮致病菌株的16SrRNA基因或16SrRNA基因区域扩增的新底漆对,以及用新底漆对鉴定和鉴定马铃薯PO病致病菌株的方法

摘要

PPROBLEM TO BE SOLVED: To provide a primer pair which is used for PCR and can strain-specifically amplify the genome DNAs of potato scab-causing strains, and to provide a method by which the specification of a strain in the speck tissues of scab-diseased tubers, the specification of the presence or absence of the scab strain and the strain in a potato field, and the specification of cultured scab fungi can quickly and simply be carried out at low costs. PSOLUTION: This primer pair for PCR hybridizes to a strain-specific base sequence of a 16SrRNA gene of the scab strain and a 16S-23S internal transcribed spacer (ITS), wherein DNA fragment sizes (base pairs) to be amplified are clearly different among the strains. A method for amplifying a genome DNA between hybridized primers, and a method for identifying an amplified product. PCOPYRIGHT: (C)2006,JPO&NCIPI
机译:

要解决的问题:提供一种用于PCR的引物对,该引物对可以菌株特异性扩增引起马铃薯strain疮的菌株的基因组DNA,并提供一种在斑点组织中鉴定菌株的方法sc病块茎的鉴定,病菌株的存在与否和马铃薯田中菌株的规格以及培养的ab疮真菌的规格可以快速,简单地以低成本进行。

解决方案:此PCR引物对与scab菌株的16SrRNA基因的菌株特异性碱基序列和16S-23S内部转录间隔子(ITS)杂交,其中要扩增的DNA片段大小(碱基对)菌株之间明显不同。一种在杂交的引物之间扩增基因组DNA的方法,以及一种鉴定扩增产物的方法。

版权:(C)2006,JPO&NCIPI

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