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一种用于检测尿液中促黄体素的“夹心”固相酶免疫测定法。

A "sandwich" solid-phase enzyme immunoassay for lutropin in urine.

作者信息

Rathnam P, Saxena B B

出版信息

Clin Chem. 1984 May;30(5):665-71.

PMID:6370499
Abstract

In this "sandwich" technique of enzyme immunoassay for lutropin in urine, a highly purified lutropin-specific anti-gamma-globulin is conjugated with alkaline phosphatase. The conjugate is then extensively purified to remove free enzyme and free antibody molecules. The solid phase consists of anti-lutropin immune globulin coupled to polystyrene tubes or beads. The specific antibody on the solid phase binds the lutropin in the urine sample or in the standard solution, which in turn binds to the specific antibody conjugated to the enzyme. The amount of bound enzyme, which is determined colorimetrically, is thus directly proportional to the amount of lutropin in the sample. We optimized assay conditions and report them here. The sensitivity of the assay is equal to that of radioimmunoassay and almost 10-fold that of the hemagglutination inhibition assay. The test can be used to detect the pre-ovulatory surge of lutropin in women.

摘要

在这种用于检测尿液中促黄体生成素的酶免疫测定“夹心”技术中,一种高度纯化的促黄体生成素特异性抗γ球蛋白与碱性磷酸酶结合。然后对结合物进行广泛纯化,以去除游离酶和游离抗体分子。固相由与聚苯乙烯管或珠子偶联的抗促黄体生成素免疫球蛋白组成。固相上的特异性抗体结合尿液样本或标准溶液中的促黄体生成素,促黄体生成素进而与偶联到酶上的特异性抗体结合。通过比色法测定的结合酶量因此与样本中促黄体生成素的量直接成正比。我们优化了测定条件并在此报告。该测定的灵敏度与放射免疫测定相同,几乎是血凝抑制测定的10倍。该测试可用于检测女性促黄体生成素的排卵前激增。

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