首页> 外文期刊>Journal of Virological Methods >Real-time RT-PCR and SYBR Green I melting curve analysis for the identification of Plum pox virus strains C, EA, and W: effect of amplicon size, melt rate, and dye translocation.
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Real-time RT-PCR and SYBR Green I melting curve analysis for the identification of Plum pox virus strains C, EA, and W: effect of amplicon size, melt rate, and dye translocation.

机译:实时RT-PCR和SYBR Green I熔解曲线分析,用于鉴定李子痘病毒C,EA和W株:扩增子大小,熔解速率和染料易位的影响。

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摘要

Real-time RT-PCR and SYBR green I melt curve analysis of a 74 bp amplicon enabled identification of Plum pox virus strains C, EA, and W, with distinct T(m)'s associated with each strain. This test is a useful supplement to a real-time RT-PCR test described earlier that was used to distinguish PPV strains D and M. A longer fragment of 155 bp was not effective for strain identification. A simplified one-tube protocol, with dithiothreitol eliminated from the reaction, showed similar sensitivity when compared to a two-tube protocol. For melt curve analysis, a slower melt rate of 0.1 degrees C/s, compared to 0.4 degrees C/s, was effective for detecting weak amplicons, and improved resolution of the T(m) of amplicons amplified simultaneously. SYBR green I was useful for duplex melt curve analysis. In repeated melt run treatments (total of 14) of a single sample containing co-amplified targets, complete translocation of SYBR green I was observed, going from a 74 bp fragment to a 114 bp fragment. The duration of the melt run may be a critical factor affecting SYBR green I binding and translocation, and its manipulation may facilitate improved resolution and simultaneous detection of multiple targets. This phenomenon may explain inconsistent SYBR green I fluorescence patterns associated with melt curve analysis of some amplicon complexes.
机译:74 bp扩增子的实时RT-PCR和SYBR green I熔解曲线分析能够鉴定梅花病毒C,EA和W株,并且每个株都有不同的T(m)。该测试是对先前所述的实时RT-PCR测试的有用补充,该实时RT-PCR测试用于区分PPV菌株D和M。更长的155 bp片段对菌株鉴定无效。与两管实验方案相比,简化的单管实验方案从反应中去除了二硫苏糖醇,显示出相似的灵敏度。对于熔解曲线分析,与0.4摄氏度/秒相比,0.1摄氏度/秒的较低熔解速率可有效检测弱扩增子,并提高了同时扩增的扩增子的T(m)的分辨率。 SYBR green I用于双链熔体曲线分析。在包含共扩增靶标的单个样品的重复熔融运行处理(总共14个)中,观察到SYBR green I的完全移位,从74 bp片段变为114 bp片段。熔解运行的持续时间可能是影响SYBR green I结合和易位的关键因素,其操作可能有助于提高分辨率并同时检测多个目标。这种现象可能解释了与某些扩增子复合物的熔解曲线分析相关的不一致的SYBR green I荧光模式。

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