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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Visual detection and microplate assay for Staphylococcus aureus based on aptamer recognition coupled to tyramine signal amplification
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Visual detection and microplate assay for Staphylococcus aureus based on aptamer recognition coupled to tyramine signal amplification

机译:基于适体识别和酪胺信号放大的金黄色葡萄球菌视觉检测和微孔板检测

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摘要

We have developed a specific method for the visual detection of Staphylococcus aureus based on aptamer recognition coupled to tyramine signal amplification technology. A biotinylated aptamer specific for S. aureus was immobilized on the surface of the wells of a microplate via biotin-avidin binding. Then, the target bacteria (S. aureus), the biotinylated-aptamer-streptavidin-HRP conjugates, biotinylated tyramine, hydrogen peroxide and streptavidin-HRP were successively placed in the wells of the microplate. After adding TMB reagent and stop solution, the intensity of the yellow reaction product can be visually inspected or measured with a plate reader. Under optimized conditions, there is a linear relationship between absorbance at 450 nm and the concentration of S. aureus in the 10 to 10~7 cfu mL concentration range (with an R2 of 0.9976). The limit of detection is 8 cfu mL~(-1).
机译:我们已经开发了一种基于适体识别和酪胺信号放大技术的金黄色葡萄球菌视觉检测方法。通过生物素-亲和素结合将对金黄色葡萄球菌特异的生物素化适体固定在微孔板的孔表面上。然后,将靶细菌(金黄色葡萄球菌),生物素化的适体-链霉亲和素-HRP缀合物,生物素化的酪胺,过氧化氢和链霉亲和素-HRP依次置于微孔板的孔中。加入TMB试剂和终止溶液后,可以通过酶标仪目视检查或测量黄色反应产物的强度。在优化的条件下,在10 nm至10〜7 cfu mL浓度范围内,450 nm处的吸光度与金黄色葡萄球菌的浓度之间存在线性关系(R2为0.9976)。检测限为8 cfu mL〜(-1)。

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