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Antibody microarray detection of Escherichia coli O157 : H7: Quantification, assay limitations, and capture efficiency

机译:大肠杆菌O157的抗体芯片检测:H7:定量,分析限制和捕获效率

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摘要

A sandwich fluorescent immunoassay in a microarray format was used to capture and detect E. coli O157:H7. Here, we explored quantitative aspects, limitations, and capture efficiency of the assay. When biotinylated capture antibodies were used, the signal generated was higher ( over 5-fold higher with some cell concentrations) compared to biotinylated protein G-bound capture antibodies. By adjusting the concentration of reporter antibody, a linear fluorescent response was observed from similar to 3.0 x 10(6) to similar to 9.0 x 10(7) cells/mL, and this was in agreement with the number of captured bacteria as determined by fluorescence microscopy. Capture efficiency calculations revealed that, as the number of bacteria presented for capture decreased, capture efficiency increased to near 35%. Optimization experiments, with several combinations of capture and reporter antibodies, demonstrated that the amount of bacteria available for capture (10(6) versus 10(8) cells/mL) affected the optimal combination. The findings presented here indicate that antibody microarrays, when used in sandwich assay format, may be effectively used to capture and detect E. coli O157: H7.
机译:微阵列形式的夹心荧光免疫测定法用于捕获和检测大肠杆菌O157:H7。在这里,我们探讨了定量方面,局限性和测定的捕获效率。当使用生物素化的捕获抗体时,与生物素化的蛋白G结合的捕获抗体相比,产生的信号更高(在某些细胞浓度下高出5倍以上)。通过调节报告抗体的浓度,可以观察到线性荧光响应,从类似于3.0 x 10(6)到类似于9.0 x 10(7)细胞/ mL,这与捕获的细菌数量相符。荧光显微镜。捕获效率的计算表明,随着要捕获的细菌数量的减少,捕获效率提高到35%。具有捕获抗体和报告抗体的几种组合的优化实验表明,可用于捕获的细菌数量(10(6)对10(8)细胞/ mL)会影响最佳组合。此处提出的发现表明,抗体微阵列以三明治测定法形式使用时,可以有效地用于捕获和检测大肠杆菌O157:H7。

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