Ran M, Dux Z, Anavi P, Witz I P
Dev Biol Stand. 1984;57:367-70.
A solid phase radioimmunoassay for cell-free antigenic mouse Fc receptor (FcR) was developed, using an 80% acetone solution for fixation of relatively large amounts of protein on PVC microtiter plates. Purified 125I labelled monoclonal anti FcR (125I-aFcR) secreted by the 2.4G2 hybridoma was used for detection and quantitation of the bound receptor. Concentrations of cell-free FcR in NP-40 extracts of FcR expressing cells were calculated from the linear part of a standard curve and expressed in units of antigenic activity - one unit being the amount of antigen capable of binding 1 microgram of 125I-aFcR. This method can be used for detecting cell-free FcR as a minor constituent in a mixture of proteins.
开发了一种用于检测无细胞抗原性小鼠Fc受体(FcR)的固相放射免疫测定法,使用80%的丙酮溶液将相对大量的蛋白质固定在PVC微量滴定板上。由2.4G2杂交瘤分泌的纯化的125I标记单克隆抗FcR(125I-aFcR)用于检测和定量结合的受体。从标准曲线的线性部分计算FcR表达细胞的NP-40提取物中无细胞FcR的浓度,并以抗原活性单位表示——一个单位是能够结合1微克125I-aFcR的抗原量。该方法可用于检测作为蛋白质混合物中次要成分的无细胞FcR。