Konijn A M, Levy R, Link G, Hershko C
J Immunol Methods. 1982 Nov 12;54(3):297-307. doi: 10.1016/0022-1759(82)90314-3.
A fluorescent enzyme-linked immunosorbent assay is described for the rapid measurement of serum ferritin. Increased sensitivity was achieved by using 4-methyl-umbelliferyl-beta-D-galactopyranoside as the substrate for beta-galactosidase coupled to the purified antiferritin antibody. Further enhancement of the specific antigen-antibody reaction was attained by the addition of 4% polyethylene glycol 6000 to the antiferritin-beta-galactosidase conjugate. The procedure is performed in microELISA plates. These modifications of the method permit the measurement of serum ferritin at concentrations ranging from 0.25 to 50 microgram/liter with a coefficient of variation of 8% or less. The entire procedure is performed at ambient temperature and is completed within one working day. The cost of the assay is less than 10% of the immunoradiometric assay for serum ferritin.
本文描述了一种用于快速测定血清铁蛋白的荧光酶联免疫吸附测定法。通过使用4-甲基伞形酮基-β-D-吡喃半乳糖苷作为与纯化的抗铁蛋白抗体偶联的β-半乳糖苷酶的底物,提高了灵敏度。通过向抗铁蛋白-β-半乳糖苷酶偶联物中添加4%聚乙二醇6000,进一步增强了特异性抗原-抗体反应。该程序在微量酶联免疫吸附测定板中进行。该方法的这些改进允许测定浓度范围为0.25至50微克/升的血清铁蛋白,变异系数为8%或更低。整个程序在室温下进行,一个工作日内即可完成。该测定法的成本不到血清铁蛋白免疫放射测定法的10%。