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A homogeneous time-resolved fluoroimmunoassay (TR-FIA) using antibody mediated luminescence quenching

机译:使用抗体介导的发光淬灭的均相时间分辨荧光免疫测定(TR-FIA)

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The determination of low-molecular weight substances (haptens) is demonstrated with a homogeneous time-resolved immunoassay using antibody-induced luminescence quenching. Our novel assay technology uses the newly developed monoclonal antibody (G24-BA9) to quench the luminescence of europium trisbipyridine (EuTBP). We performed a competitive biotin immunoassay including an EuTBP–biotin conjugate, the anti-EuTBP antibody G24-BA9 and streptavidin as assay components. Steric hindrance allows only the binding of either G24-BA9 (to the EuTBP moiety) or streptavidin (to the biotin moiety) to the EuTBP–biotin conjugate. Addition of the analyte biotin resulted in the binding of streptavidin to biotin and a concomitant preferred binding of G24-BA9 to EuTBP–biotin. Since G24-BA9 quenches the luminescence of EuTBP within the conjugate, the luminescence signal could be used to indicate and quantify the presence of free biotin in the system. All experiments were carried out in solution in the presence of 5% serum demonstrating the possibility of using our novel assay for a very fast determination of low molecular weight substances in biological fluids...
机译:低分子量物质(半抗原)的测定通过使用抗体诱导的发光淬灭的均相时间分辨免疫测定法进行证明。我们新颖的测定技术使用新开发的单克隆抗体(G24-BA9)来淬灭tri三联吡啶(EuTBP)的发光。我们进行了竞争性生物素免疫测定,包括EuTBP-生物素结合物,抗EuTBP抗体G24-BA9和链霉亲和素作为测定成分。立体位阻仅允许G24-BA9(与EuTBP部分结合)或链霉亲和素(与生物素部分结合)与EuTBP-生物素结合物结合。加入分析物生物素可导致链霉亲和素与生物素结合,并伴有G24-BA9与EuTBP-生物素的优选结合。由于G24-BA9淬灭了缀合物中EuTBP的发光,因此该发光信号可用于指示和定量系统中游离生物素的存在。所有实验均在5%血清存在下于溶液中进行,这表明使用我们的新型测定法非常快速地测定生物流体中低分子量物质的可能性...

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