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首页> 外文期刊>Integrative Biology: quantitative biosciences from nano to macro >Detection of microalgae superoxide dismutase (SOD) using a GNRs-based resonance light scattering system
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Detection of microalgae superoxide dismutase (SOD) using a GNRs-based resonance light scattering system

机译:利用GNRS谐振光散射系统检测微血糖超氧化物歧化酶(SOD)

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摘要

A novel and label-free, gold nanorods (GNRs)-based resonance light scattering system assay has been developed for the detection of microalgae superoxide dismutase (SOD). The method relies on the fact that interactions between microalgae SOD and GNRs can emit strong fluorescence signals. The prepared GNRs were well dispersed in the solution and intracellular SOD was extracted from Microcystis aeruginosa; the SOD was then absorbed on the surface of the GNRs. The results demonstrated that the intensity of the fluorescence signals increased at 595 nm with an increase in the SOD concentration, the optimum pH value was concluded to be 7.8, the optimum concentration of inorganic salt Na+ ions was 0.2 mol L-1, and the reaction system was stable for 50 min. This method offers the advantages of higher sensitivity and selectivity in microalgae protein detection and exhibits great potential for biological diagnosis.
机译:已经开发了一种新颖的和无标记的金纳米棒(GNR)的基于谐振光散射系统测定,用于检测微藻超氧化物歧化酶(SOD)。 该方法依赖于微藻和GNR之间的相互作用可以发射强荧光信号。 将制备的GNRS分散在溶液中,从微囊杆菌铜绿假单胞菌中提取细胞内SOD; 然后将SOD吸收在GNR的表面上。 结果表明,荧光信号的强度在595nm增加,加入SOD浓度增加,最佳pH值得出到7.8,无机盐Na +离子的最佳浓度为0.2mol L-1,以及反应 系统稳定50分钟。 该方法提供了微藻蛋白检测中敏感性和选择性更高的优点,并且对生物诊断具有巨大潜力。

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