Khosravi M J, Chan M A, Bellem A C, Diamandis E P
CyberFluor Inc., Toronto, Ontario, Canada.
Clin Chim Acta. 1988 Jul 29;175(3):267-75. doi: 10.1016/0009-8981(88)90102-7.
We describe a new non-isotopic immunoassay for the quantitation of ferritin in serum. Ferritin is first immunoextracted from serum with a monoclonal antibody immobilized in white microtiter wells. A second biotinylated antibody is then added. The bound biotinylated antibody is quantified by a bridge reaction with streptavidin labeled with the europium chelate 4,7-bis(chlorosulfophenyl)-1,10-phenanthroline-2,9-dicarboxylic acid (BCPDA) in the presence of excess Eu3+. The fluorescence on the bottom of the dry microtiter well consisting of monoclonal antibody-ferritin-monoclonal antibody-biotin-streptavidin-BCPDA-Eu3+ is then measured with a time-resolved fluorometer. The assay is sensitive (0.5 microgram/l), precise (CV's 3-9%) and accurate (average recovery 102%). Results compared well (r = 0.99) with those of a widely used RIA procedure.
我们描述了一种用于定量血清中铁蛋白的新型非同位素免疫测定法。首先用固定在白色微量滴定孔中的单克隆抗体从血清中免疫提取铁蛋白。然后加入第二种生物素化抗体。在过量Eu3+存在的情况下,通过与用铕螯合物4,7-双(氯磺苯基)-1,10-菲咯啉-2,9-二羧酸(BCPDA)标记的链霉亲和素进行桥连反应来定量结合的生物素化抗体。然后用时间分辨荧光计测量由单克隆抗体-铁蛋白-单克隆抗体-生物素-链霉亲和素-BCPDA-Eu3+组成的干燥微量滴定孔底部的荧光。该测定法灵敏(0.5微克/升)、精确(变异系数3-9%)且准确(平均回收率102%)。结果与广泛使用的放射免疫分析方法的结果相比良好(r = 0.99)。