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首页> 外文期刊>Journal of Veterinary Diagnostic Investigation >Development of a reverse transcription loop-mediated isothermal amplification assay for detection of Porcine teschovirus.
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Development of a reverse transcription loop-mediated isothermal amplification assay for detection of Porcine teschovirus.

机译:建立反转录环介导的等温扩增检测猪瘟细小病毒的方法。

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摘要

Loop-mediated isothermal amplification (LAMP) is a sensitive method for DNA amplification. In the present report, the development of a single-tube, one-step, real-time accelerated reverse transcription (RT)-LAMP for the detection of Porcine teschovirus (PTV) is described. Six designed primers amplified target gene sequences successfully at constant temperature (65 degrees C) within 1 hr, and the amplification results could be visualized directly by the naked eye. The sensitivity of the LAMP was 10 times higher than that of conventional polymerase chain reaction, and no cross-reactivity was found when the genomes of other common swine pathogens were subjected to the RT-LAMP system. When 43 clinical samples were tested by the RT-LAMP method, results indicated that the test is simple, rapid, accurate, and sensitive for the detection of PTV.
机译:环介导的等温扩增(LAMP)是DNA扩增的灵敏方法。在本报告中,描述了单管,一步一步,实时加速逆转录(RT)-LAMP的开发,用于检测猪瘟病毒(PTV)。 6个设计好的引物在1小时内于恒定温度(65℃)成功扩增了目标基因序列,扩增结果可以通过肉眼直接观察到。 LAMP的灵敏度是常规聚合酶链反应的10倍,当其他常见猪病原体的基因组经过RT-LAMP系统处理时,没有发现交叉反应。用RT-LAMP方法对43个临床样品进行检测时,结果表明该检测方法简单,快速,准确且对检测PTV敏感。

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