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首页> 外文期刊>Fresenius' Journal of Analytical Chemistry >Fluoresence immunoassay of alpha-fetoprotein with iron(III) tetrasulfonatophthalocyanine as a mimetic enzyme labeling reagent
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Fluoresence immunoassay of alpha-fetoprotein with iron(III) tetrasulfonatophthalocyanine as a mimetic enzyme labeling reagent

机译:四磺酸铁(酞菁酞菁铁)作为模拟酶标记试剂的甲胎蛋白的荧光免疫测定

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摘要

A new fluorimetric immunoassay for a-fetoprotein (AFP) has been developed using a novel promising mimetic peroxidase, iron(III) tetrasulfonatophthalocyanine (FeTSPc). as a labeling reagent to catalyze the fluorescence reaction of P-hydroxyphenylacetic acid (P-HPA) and hydrogen peroxide (H2O2) In the competitive immunoassay, anti-AFP antibody was coated on a 96-well plate (polystyrene) and a constant amount of FeTSPc-labeled AFP and a known amount of test solution were added. Non-labeled and FeTSPc-labeled AFP compete for binding to the plate-bound antibody. After the immunoreaction, the immunochemically adsorbed FeTSPc-AFP conjugate moiety was determined by measuring the fluorescence produced in a solution containing P-HPA and H2O2. AFP can be determined in the concentration range of 1-300 ng mL(-1) with a detection limit of 0.5 ng mL(-1). [References: 12]
机译:已经开发了一种使用新型有希望的模拟过氧化物酶,铁(III)四磺酰萘酞菁(FeTSPc)的α-甲胎蛋白(AFP)的新型荧光免疫测定法。作为标记试剂以催化P-羟苯基乙酸(P-HPA)和过氧化氢(H2O2)的荧光反应在竞争性免疫测定中,将抗AFP抗体包被在96孔板(聚苯乙烯)上,并恒定量的加入FeTSPc标记的AFP和已知量的测试溶液。未标记的和FeTSPc标记的AFP竞争与板结合抗体的结合。免疫反应后,通过测量在含有P-HPA和H2O2的溶液中产生的荧光来确定免疫化学吸附的FeTSPc-AFP缀合物部分。可以在1-300 ng mL(-1)的浓度范围内测定AFP,检出限为0.5 ng mL(-1)。 [参考:12]

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