首页> 外文会议>International Conference on Biomedical Engineering and Biotechnology >Using Loop-mediated Isothermal DNA Amplification (LAMP) and Spectral Surface Plasmon Resonance (SPR) to Detect Methicillin-resistance S. aureus (MRSA)
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Using Loop-mediated Isothermal DNA Amplification (LAMP) and Spectral Surface Plasmon Resonance (SPR) to Detect Methicillin-resistance S. aureus (MRSA)

机译:使用环介导的等温DNA扩增(灯)和光谱表面等离子体共振(SPR)以检测甲氧西林抗性S. aureus(MRSA)

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Loop-mediated isothermal amplification (LAMP) is a rapid (within an hour) and sensitive method to amplify DNA at one temperature. It has a high potential to be used as a biosensor to detect pathogens as LAMP does not require thermal cycles to amplify DNA. On the other hand, surface plasmon resonance (SPR) is a highly sensitive optical system for label-free biomolecules detection. With these advantages, we tried to combine SPR and LAMP to detect the gene of Panton-Valentine leukocidin toxin (pvl) of Methicillin-resistance S. aureus (MRSA). Our preliminary data indicate that the LAMP amplification products (lamplicons) of pvl showed an obvious spectrum shift when monitored by SPR. Our data suggest that using SPR to sense the LAMP products is a new approach for real-time biosensing.
机译:环介导的等温扩增(灯)是快速(在一个小时内)和敏感方法,以在一次温度下扩增DNA。它具有用作生物传感器的高潜力以检测病原体,因为灯不需要热循环以扩增DNA。另一方面,表面等离子体共振(SPR)是一种高敏感的光学系统,用于无标记的生物分子检测。通过这些优点,我们试图结合SPR和灯来检测肝炎抗胰岛素抗金黄色葡萄球菌(MRSA)的Panton-valentine毒素毒素(PVL)的基因。我们的初步数据表明,PVL的灯放大产品(Lamplicons)在SPR监测时显示出明显的频谱移位。我们的数据表明,使用SPR感测灯产品是实时生物传感的新方法。

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