Mongini P K, Heber-Katz E
J Immunol Methods. 1982;49(1):39-52. doi: 10.1016/0022-1759(82)90364-7.
A slid-phase radioimmunoassay (RIA) for assaying immunoglobulin produced from antibody-secreting myeloma, hybridoma and immune spleen cells is described. Specific antibody is detected by culturing antibody-producing cells on antigen-coated flexible polyvinylchloride microtiter wells, washing away the cells, and measuring the bound specific antibody with tritiated affinity-purified anti-isotype reagents. Antibody produced from 10(3) myeloma cells can be detected with as little as 4 h of incubation. With 24-48 h of incubation, antibody from as few as approximately 3-15 myeloma, hybridoma or immune spleen plaque-forming cells (PFC) can be detected. This culture-well RIA has certain distinct advantages over the hemolytic PFC assay and RIA assays in which antibody in culture supernatants is measured.
本文描述了一种用于检测由分泌抗体的骨髓瘤细胞、杂交瘤细胞和免疫脾细胞产生的免疫球蛋白的固相放射免疫测定法(RIA)。通过将产生抗体的细胞培养在包被有抗原的柔性聚氯乙烯微量滴定板孔中,洗去细胞,并用氚标记的亲和纯化抗同种型试剂测量结合的特异性抗体,来检测特异性抗体。10³个骨髓瘤细胞产生的抗体在孵育仅4小时后即可被检测到。经过24 - 48小时的孵育,少至约3 - 15个骨髓瘤细胞、杂交瘤细胞或免疫脾空斑形成细胞(PFC)产生的抗体也能被检测到。这种培养孔RIA与溶血PFC测定法以及测量培养上清液中抗体的RIA测定法相比,具有某些明显的优势。