类风湿因子
类毒素
多克隆抗体
单克隆抗体
化学
单克隆
免疫复合物
琼脂糖
补体因子I
免疫系统
抗血清
补体系统
免疫学
分子生物学
抗体
医学
生物化学
生物
酶
免疫
作者
Guido Vanham,Frans Bloemmen,Jan L. Ceuppens,Erik Stevens
标识
DOI:10.1016/0022-1759(84)90405-8
摘要
Soluble purified monoclonal and polyclonal rheumatoid factor, total serum complement, and soluble C1q all inhibit the detection of model tetanus toxoid/anti-toxoid immune complexes in the solid-phase C1q assay. The binding of these immune complexes to solid-phase monoclonal rheumatoid factor is less inhibited by soluble C1q and by total serum complement, but clearly decreased by soluble monoclonal or polyclonal rheumatoid factor. Serum complement does not reduce the size of these model complexes. We recommend the use of low ionic strength EDTA (10 mM) to partly neutralize the complement-mediated inhibition. This procedure is shown to be superior to currently used higher EDTA concentrations and to the use of IgG-Sepharose.
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