Adám E, Nász I, Lengyel A, Erdei J, Fachet J
Acta Microbiol Hung. 1986;33(4):317-24.
The feasibility of using monoclonal antibodies to capture specific viral polypeptides in double monoclonal antibody (MAb) sandwich ELISA has been demonstrated. Ten MAbs with different reactivity patterns were used for antigen capture and four of them were labelled with horse radish peroxidase and used for the detection of specifically bound hexon antigen and for the determination of the lowest reacting hexon concentrations. Differences have been found in the effectiveness of the different MAbs used for capturing or detecting the antigen. Two assay systems (MAbs 1A3/1A3 and H12/1A3), which were the most sensitive for the hexon types studied could be useful for detection of the adenovirus hexons. Assay system MAb 2D1/2A1 and several combinations of MAb 2B2 proved to be specific for subgenus C.
在双单克隆抗体(MAb)夹心酶联免疫吸附测定(ELISA)中,使用单克隆抗体捕获特定病毒多肽的可行性已得到证实。使用了10种具有不同反应模式的单克隆抗体进行抗原捕获,其中4种用辣根过氧化物酶标记,用于检测特异性结合的六邻体抗原以及确定最低反应性六邻体浓度。已发现用于捕获或检测抗原的不同单克隆抗体的有效性存在差异。对于所研究的六邻体类型最敏感的两种检测系统(单克隆抗体1A3/1A3和H12/1A3)可用于检测腺病毒六邻体。检测系统单克隆抗体2D1/2A1和单克隆抗体2B2的几种组合被证明对C亚属具有特异性。