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A method for detecting M. tuberculosis genotype VEIJING IN REAL TIME

机译:实时检测结核分枝杆菌基因型VEIJING的方法

摘要

FIELD: medicine, pharmaceutics.;SUBSTANCE: invention refers to medicine and microbiology. What is presented is a method for real-time detection of Beijing genotype mycobacterium tuberculosis by detecting IS6110 element insertion in a locus of dnaA-dnaNgenome differing by the fact that real-time PCR is carried out with the use of two specific primers5`-AGATCAGAGAGTCTCCGGACTCA and 5`-CGCCGGGACTGTATGAGTCT and fluorescence-labelled probe R6G-5`-TGTGCACAGCGACACTCACAGCCA-3`-BHQ2; the result is assessed by recording a fluorescence signal in R6G canal at wavelength 555nm; if a sample contains the DNA of the Beijing genotype mycobacterium tuberculosis strain, an exponential growth of the PCR fluorescence signal when a pure DNA analysed is observed between 10 to 15 cycles, and when cell lysates analysed - between 15 and 20 cycles.;EFFECT: invention can be used for laboratory detection of Beijing genotype mycobacterium tuberculosis.;3 dwg, 2 ex
机译:领域:药物,药物;物质:发明是指药物和微生物学。本文提出了一种通过检测dnaA-dnaN基因组位点中IS6110元素插入来实时检测北京基因型结核分枝杆菌的方法,该方法的不同之处在于使用两种特异性引物进行实时PCR5'-AGATCAGAGAGTCTCCGGACTCA 5'-CGCCGGGACTGTATGAGTCT和荧光标记探针R6G-5`-TGTGCACAGCGACACTCACAGCCA-3`-BHQ2;通过在波长555nm的R6G管中记录荧光信号来评估结果。如果样品中含有北京基因型结核分枝杆菌菌株的DNA,则在10到15个循环之间观察到纯DNA的分析,在15到20个循环之间观察到细胞裂解液的观察到的PCR荧光信号的指数增长。本发明可用于北京基因型结核分枝杆菌的实验室检测。3 dwg,2 ex

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