Bedford D K, Shepherd J, Morgan H G
Clin Chim Acta. 1976 Jul 15;70(2):267-76. doi: 10.1016/0009-8981(76)90428-9.
We have developed a simplified double antibody radioimmunoassay for human apolipoprotein beta. The purified antigen, a narrow density subclass of beta lipoprotein (d 1.030-1.050 g/ml; was isolated by a combination of gel filtration and ultracentrifugationmthis material gave a single immunoprecipitin arc on crossed immunoelectrophoresis into an antibody to whole human serum. The antigen was radiolabelled using iodine monochloride at pH 10. The iodinated antigen was indistinguishable immunochemically from native material and eluted as a single radioactive peak from a Sephadex G-200 column. The lower limit of sensitivity of the assay was 15 ng protein, and the working range, 15-200 ng. The mean apolipoprotein B level (+/-1 S.D.) in 128 healthy control subjects was 86.6 +/- 29.6 mg/100ml and is in agreement the values published by other workers using unmodified assays.
我们已经开发出一种用于检测人载脂蛋白β的简化双抗体放射免疫分析法。纯化的抗原是β脂蛋白的一个狭窄密度亚类(d 1.030 - 1.050 g/ml),通过凝胶过滤和超速离心相结合的方法分离得到;该物质在与抗全人血清抗体进行交叉免疫电泳时产生单一免疫沉淀弧。抗原在pH 10条件下用一氯化碘进行放射性标记。碘化抗原在免疫化学性质上与天然物质无法区分,并且从Sephadex G - 200柱上以单一放射性峰洗脱。该分析方法的灵敏度下限为15 ng蛋白质,工作范围为15 - 200 ng。128名健康对照受试者的载脂蛋白B平均水平(±1标准差)为86.6 ± 29.6 mg/100ml,这与其他研究人员使用未改良分析方法所发表的值一致。