16S rDNA-DGGE와 real-time PCR 증폭을 이용한 세균군집 분석법
    1.
    发明公开
    16S rDNA-DGGE와 real-time PCR 증폭을 이용한 세균군집 분석법 无效
    使用16S RDNA-DGGE和实时PCR的细菌群落分析方法

    公开(公告)号:KR1020110066018A

    公开(公告)日:2011-06-16

    申请号:KR1020090122747

    申请日:2009-12-10

    CPC classification number: C12Q1/6844 C12Q2527/137 G01N27/447

    Abstract: PURPOSE: A method for analyzing bacteria community using 16S rDNA-DGGE and real-time PCR is provided to minimize analysis error. CONSTITUTION: A method for analyzing bacteria community using 16S rDNA-DGGE and real-time PCR comprises: a step of performing PCR amplification using 0.25-0.375 mM of dNTP concentration; or a step of performing real-time PCR using bacteria DNA as a template and primers; a step of performing DGGE of PCR products to measure PCR band intensity; and a step of calculating ratio of bacteria species based on the number and intensity of the bands.

    Abstract translation: 目的:提供使用16S rDNA-DGGE和实时PCR分析细菌群落的方法,以尽量减少分析误差。 构成:使用16S rDNA-DGGE和实时PCR分析细菌群落的方法包括:使用0.25-0.375mM dNTP浓度进行PCR扩增的步骤; 或使用细菌DNA作为模板和引物进行实时PCR的步骤; 进行PCR产物DGGE测量PCR带强度的步骤; 以及根据带的数量和强度计算细菌种类的比例的步骤。

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