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One-step antibody immobilization-based rapid and highly-sensitive sandwich ELISA procedure for potential in vitro diagnostics

机译:基于一步抗体固定化的快速,高度灵敏的夹心ELISA程序用于潜在的体外诊断

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An improved enzyme-linked immunosorbent (ELISA) assay using one-step antibody immobilization has been developed for the detection of human fetuin A (HFA), a specific biomarker for atherosclerosis and hepatocellular carcinoma. The anti-HFA formed a stable complex with 3-aminopropyltriethoxysilane (APTES) by ionic and hydrophobic interactions. The complex adsorbed on microtiter plates exhibited a detection range of 4.9?pg mL?1 to 20?ng mL?1 HFA, with a limit of detection of 7?pg mL?1. Furthermore, an analytical sensitivity of 10?pg mL?1 was achieved, representing a 51-fold increase in sensitivity over the commercial sandwich ELISA kit. The results obtained for HFA spiked in diluted human whole blood and plasma showed the same precision as the commercial kit. When stored at 4°C in 0.1?M phosphate-buffered saline (PBS, pH 7.4), the anti-HFA bound microtiter plates displayed no significant decrease in their functional activity after two months. The new ELISA procedure was extended for the detection of C-reactive protein, human albumin and human lipocalin-2 with excellent analytical performance.
机译:已开发出一种使用一步抗体固定化的改进的酶联免疫吸附(ELISA)分析方法,用于检测人胎球蛋白A(HFA),这是动脉粥样硬化和肝细胞癌的一种特定生物标记。抗-HFA通过离子和疏水作用与3-氨丙基三乙氧基硅烷(APTES)形成稳定的络合物。微量滴定板上吸附的复合物的检测范围为4.9?pg mL ?1 至20?ng mL ?1 HFA,检出限为7?pg mL ?1 。此外,分析灵敏度达到了10?pg mL ?1 ,比市售夹心ELISA试剂盒灵敏度提高了51倍。在稀释的人全血和血浆中加标HFA的结果显示出与市售试剂盒相同的精度。当在4°C下于0.1?M磷酸盐缓冲盐水(PBS,pH 7.4)中保存时,结合有抗HFA的微量滴定板在两个月后未显示其功能活性明显降低。新的ELISA程序被扩展用于检测C反应蛋白,人白蛋白和人lipocalin-2,具有出色的分析性能。

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