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Highly sensitive and rapid tandem bioluminescent immunoassay using aequorin labeled Fab fragment and biotinylated firefly luciferase

机译:使用水母发光蛋白标记的Fab片段和生物素化萤火虫荧光素酶的高灵敏快速串联生物发光免疫测定

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摘要

We established a simultaneous bioluminescent assay utilizing aequorin (Aq) and biotinylated firefly luciferase (b-Luc);furthermore,we developed a highly sensitive and rapid tandem bioluminescent immunoassay (BLIA) involving the Aq-labeled Fab fragment and b-Luc-streptavidin complex.Minimum detection limits of Aq and b-Luc were 9.4 x 10~(-21) mol assay~(-1) (blank + 3S.D.) and 3.6 x 10~(-19) mol assay~(-1)(blank+3S.D.),respectively.Measurements of two luminescent proteins were completed in 4 s with a single assay medium.In this study,prostatic acid phosphatase (PAP) and prostate specific antigen (PSA),which served as analytes,were measured in the tandem BLIA.PAP and PSA were detected by the Aq-labeled anti-Dig Fab fragment and b-Luc-streptavidin complex,respectively.The measurable ranges of PAP and PSA were 0.04-100 and 0.2-200 ng mL-1,respectively.This technique was also applied to the simultaneous measurement of PSA and a-fetoprotein (AFP).Measurable ranges of PSA and AFP were 0.2-200 and 1.95-1000 ng mL-1,respectively.Levels of PAP and PSA or PSA and AFP in human serum could be accurately determined with the proposed BLIA.Satisfactory correlations were observed between results obtained from the proposed BLIA and those derived from commercial kits.
机译:我们利用水母发光蛋白(Aq)和生物素化萤火虫荧光素酶(b-Luc)建立了同时的生物发光测定法;此外,我们开发了一种高灵敏度,快速的串联生物发光免疫测定法(BLIA),涉及Aq标记的Fab片段和b-Luc-链霉亲和素复合物Aq和b-Luc的最低检测限为9.4 x 10〜(-21)mol检测〜(-1)(空白+ 3S.D.)和3.6 x 10〜(-19)mol检测〜(-1) (分别为空白+ 3S.D。)。使用单一测定介质在4 s内完成了两种发光蛋白的测量。在这项研究中,前列腺酸性磷酸酶(PAP)和前列腺特异性抗原(PSA)作为分析物,在串联BLIA中进行检测.PAP和PSA分别通过Aq标记的抗Dig Fab片段和b-Luc-链霉亲和素复合物检测.PAP和PSA的可测量范围为0.04-100和0.2-200 ng mL- 1,分别用于PSA和甲胎蛋白(AFP)的同时测量.PSA和AFP的可测量范围为0.2-200建议的BLIA可以准确测定人血清中PAP和PSA或PSA和AFP的水平。从建议的BLIA获得的结果与从商业试剂盒获得的结果之间存在令人满意的相关性。

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