Kato K, Umeda Y, Suzuki F, Hayashi D, Kosaka A
Clin Chem. 1979 Jul;25(7):1306-8.
We describe a "sandwich-type" enzyme immunoassay for insulin in serum, in which antibody Fab'-beta-D-galactosidase conjugate and an antibody-immobilized silicone rubber solid-phase are used. The interference by serum factors with the solid-phase enzyme immunoassay can now be removed by using a buffer containing gelatin. Serum samples of 50 microL can be analyzed by the enzyme immunoassay, which is as sensitive as radioimmunoassay for human insulin. Our results correlate well with those for radioimmunoassay (r = 0.97, slope = 0.92, y-intercept = 4.6 milli-int. units /L for 181 samples). Between-assay and within-assay coefficients of variation are less than 15% over the useful ranges of the assay (5--160 milli-int. units/L).
我们描述了一种用于血清中胰岛素检测的“夹心型”酶免疫测定法,该方法使用抗体Fab'-β-D-半乳糖苷酶结合物和固定有抗体的硅橡胶固相。现在,通过使用含有明胶的缓冲液,可以消除血清因子对固相酶免疫测定的干扰。酶免疫测定法可分析50微升的血清样本,其对人胰岛素的敏感性与放射免疫测定法相同。我们的结果与放射免疫测定法的结果相关性良好(181个样本的r = 0.97,斜率 = 0.92,截距 = 4.6毫国际单位/升)。在该测定法的有效范围内(5 - 160毫国际单位/升),批间和批内变异系数均小于15%。