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Immunoelectrochemical assay in combination with homogeneous enzyme-labeled antibody conjugation for rapid detection of Salmonella

机译:免疫电化学分析结合均相酶标记抗体偶联可快速检测沙门氏菌

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摘要

An immunoelectrochemical assay in combination with homogeneous enzyme-labeled antibody conjugation was developed for rapid detection of Salmonella. The assay was performed by mixing alkaline phosphatase linked anti-Salmonella (APLAS) with Salmonella in a solution. The Salmonella-APLAS conjugate separated by polycarbonate membrane filtration was incubated with a phenyl phosphate substrate to produce phenol. The concentration of Salmonella cells was determined by measuring phenol oxidation peak current using differential pulse voltammetry at a renewable carbon paste electrode. This assay could be completed within two hours with a detection limit of 5 x 10(3) cells/mL. A linear response was found for Salmonella between 5 x 10(3) and 1 x 10(6) cells/mL. [References: 16]
机译:建立了一种免疫电化学检测方法,结合了均相酶标记的抗体结合物,可快速检测沙门氏菌。通过将碱性磷酸酶连接的抗沙门氏菌(APLAS)与沙门氏菌在溶液中混合进行测定。将通过聚碳酸酯膜过滤分离的沙门氏菌-APLAS共轭物与磷酸苯酯底物一起孵育以生产苯酚。沙门氏菌细胞的浓度是通过在可再生碳糊电极上使用差分脉冲伏安法测量酚氧化峰值电流来确定的。该检测可以在两个小时内完成,检测极限为5 x 10(3)个细胞/ mL。发现沙门氏菌的线性响应介于5 x 10(3)和1 x 10(6)细胞/ mL之间。 [参考:16]

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