Schiller H S, Kulchinski L, Luthy D A
Clin Chem. 1978 Feb;24(2):275-9.
We report a relatively simple and convenient method for iodinating human alpha-fetoprotein and for purifying the 125I-labeled material. The label is incorporated into human alpha-fetoprotein enzymatically by use of lactoperoxidase. Before each assay the labeled material is purified over two successive short columns: Sepharcryl S-200 Superfine and cellulose. This procedure removes both free iodine and "damaged" fetoprotein. With the purified material we developed a sensitive and reliable radioimmunoassay for alpha-fetoprotein in serum and amniotic fluid.
我们报告了一种相对简单便捷的方法,用于对人甲胎蛋白进行碘化以及纯化碘-125标记的物质。通过使用乳过氧化物酶,将标记物酶促掺入人甲胎蛋白中。在每次测定之前,将标记物质先后通过两根短柱进行纯化:Sepharcryl S - 200 Superfine柱和纤维素柱。此步骤可去除游离碘和“受损”的胎蛋白。利用纯化后的物质,我们开发了一种灵敏且可靠的用于检测血清和羊水中甲胎蛋白的放射免疫测定法。