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采用双标记时间分辨免疫荧光分析法同时检测甲胎蛋白和人绒毛膜促性腺激素游离β亚基。

Simultaneous assay of alpha-fetoprotein and free beta subunit of human chorionic gonadotropin by dual-label time-resolved immunofluorometric assay.

作者信息

Pettersson K, Alfthan H, Stenman U H, Turpeinen U, Suonpää M, Söderholm J, Larsen S O, Nørgaard-Pedersen B

机构信息

Wallac Oy, Turku, Finland.

出版信息

Clin Chem. 1993 Oct;39(10):2084-9.

PMID:7691439
Abstract

We developed a simple, rapid two-step dual-label assay for the noncompetitive determination of alpha-fetoprotein (AFP) and beta subunit of human chorionic gonadotropin (hCG beta) in serum. Monoclonal antibodies to detect AFP and hCG beta were labeled with europium (Eu) and samarium (Sm), respectively. Highly fluorescent chelates were developed by using the Delfia enhancement principle. The detection limits for AFP and hCG beta were approximately 0.02 kIU/L and approximately 0.2 IU/L, respectively. The within-run precision was < 5% over the whole range of AFP (1-500 kIU/L) and hCG beta (1-200 IU/L) concentrations tested. Cross-reaction of intact hCG was < 0.03%. The AFP concentrations determined with the dual-label assay correlated well with those obtained by Delfia AFP single-label kit. The concentrations of hCG beta were in good agreement with recently published data. Storing the serum samples for 24 h or 1 week at room temperature increased the hCG beta concentration by 4% and 26%, respectively. At 35 degrees C this dissociation of hCG increased 30-40-fold. Repeated freezing and thawing had no effect on the hCG beta concentration.

摘要

我们开发了一种简单、快速的两步双标记检测法,用于血清中甲型胎儿蛋白(AFP)和人绒毛膜促性腺激素β亚基(hCGβ)的非竞争性测定。分别用铕(Eu)和钐(Sm)标记检测AFP和hCGβ的单克隆抗体。利用时间分辨荧光免疫分析增强原理生成高荧光螯合物。AFP和hCGβ的检测限分别约为0.02 kIU/L和约0.2 IU/L。在所测试的AFP(1 - 500 kIU/L)和hCGβ(1 - 200 IU/L)浓度的整个范围内,批内精密度<5%。完整hCG的交叉反应<0.03%。用双标记检测法测定的AFP浓度与用时间分辨荧光免疫分析AFP单标记试剂盒获得的浓度相关性良好。hCGβ的浓度与最近发表的数据高度一致。在室温下将血清样本储存24小时或1周,hCGβ浓度分别增加4%和26%。在35摄氏度时,hCG的这种解离增加30 - 40倍。反复冻融对hCGβ浓度没有影响。

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