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Comparison of Reverse Transcription Loop-Mediated Isothermal Amplification Method with SYBR Green Real-Time RT-PCR and Direct Fluorescent Antibody Test for Diagnosis of Rabies

机译:逆转录环介导等温扩增法与SYBR绿色实时RT-PCR和直接荧光抗体试验进行肝癌

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Rabies as an endemic disease in most Asian and African countries, especially in remote areas, and requires a reliable diagnostic method. This study aimed to develop a reverse transcription loop-mediated isothermal amplification (RT-LAMP) method for rapid detection of rabies virus RNA in the brain samples, compared to SYBR Green real time RT-PCR test as a molecular technique and direct fluorescent antibody test as a serological method. In this study, RT-LAMP was developed to diagnose rabies. Six primers were designed based on the nucleoprotein (N) of rabies virus. The sensitivity and specificity of SYBR Green real-time RT-PCR and RT-LAMP methods were also determined.
机译:狂犬病作为大多数亚洲和非洲国家的流行病,特别是在偏远地区,需要一种可靠的诊断方法。本研究旨在开发逆转录回归介导的等温扩增(RT灯)方法,用于快速检测脑样品中的狂犬病病毒RNA,与Sybr绿色实时RT-PCR试验作为分子技术和直接荧光抗体试验相比作为一种血清学方法。在这项研究中,开发了RT灯以诊断狂犬病。基于狂犬病病毒的核蛋白(N)设计了六个引物。还确定了SYBR绿色实时RT-PCR和RT灯方法的敏感性和特异性。

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