Bode L, Pocchiari M, Gelderblom H, Diringer H
J Gen Virol. 1985 Nov;66 ( Pt 11):2471-8. doi: 10.1099/0022-1317-66-11-2471.
Antisera raised in rabbits and also for the first time in mice against scrapie-associated fibril (SAF) protein from hamster brain have been quantified by a modified ELISA technique (NC-ELISA) and used for a detailed analysis of SAF proteins obtained from hamster, mouse, and from patients who died of Creutzfeldt-Jakob disease. The antisera predominantly detected five bands in a Western blot analysis with apparent molecular weights of about 26000 (26K), 24K, 20K, 18K and 16K. By gel electrophoresis these antigens seem to be identical in mouse, hamster and man. The amount of material in the various bands, however, varies according to host or agent. In control materials from healthy brain SAF protein was found to be absent even when this material was used in a 50-fold excess compared to diseased brain.
用改良酶联免疫吸附测定技术(NC-ELISA)对首次在小鼠以及在兔中产生的、针对来自仓鼠脑的瘙痒病相关纤维(SAF)蛋白的抗血清进行了定量,并用于详细分析从仓鼠、小鼠以及死于克雅氏病的患者体内获得的SAF蛋白。在用蛋白质印迹分析时,这些抗血清主要检测到五条带,其表观分子量约为26000(26K)、24K、20K、18K和16K。通过凝胶电泳,这些抗原在小鼠、仓鼠和人类中似乎是相同的。然而,各条带中的物质含量根据宿主或病原体的不同而有所变化。在来自健康脑的对照材料中,即使与患病脑相比使用了50倍过量的该材料,也未发现SAF蛋白。