Marchev N, Veleva E, Bazhlekov N
Vet Med Nauki. 1979;16(1):13-7.
The coupling of the F. M. D. antigen with unsoluble CNBr-activated sepharose (2B or 4B) induced the production of an active agent with which the specific F. M. D. antibody of the investigated solution may covalently couple. Coupling procedures prove most effective with the use of buffer solutions of high ion strength that is necessary for the reduction of a protein-protein adsorption initiated by the polyoelectrolite nature of proteins. The produced complexes of the type CNBr activated sepharose--12C antigen--antibody after elimination of the unspecific serum proteins are dissociated up to the release of a specific IgG antibody.
F.M.D.抗原与不溶性溴化氰活化琼脂糖(2B或4B)偶联,诱导产生一种活性剂,被研究溶液中的特异性F.M.D.抗体可与其共价偶联。使用高离子强度的缓冲溶液时偶联程序证明最为有效,这对于减少由蛋白质的聚电解质性质引发的蛋白质-蛋白质吸附是必要的。在去除非特异性血清蛋白后,所产生的溴化氰活化琼脂糖-12C抗原-抗体复合物解离直至释放出特异性IgG抗体。