Adams D S, Gogolewski R P, Barbet A F, Cheevers W P
J Gen Virol. 1985 May;66 ( Pt 5):1139-43. doi: 10.1099/0022-1317-66-5-1139.
Precipitin lines formed between serum from a goat infected with caprine arthritis-encephalitis virus (CAEV) and radiolabelled viral proteins in polyethylene glycol-concentrated culture medium were excised from immunodiffusion (ID) plates and analysed by polyacrylamide gel electrophoresis. The two major precipitin lines contained the 135 000 mol. wt. glycoprotein (gp 135) and the internal 28 000 mol. wt. structural protein (p28). This method obviates the use of purified proteins or monospecific antisera to positively determine viral constituents in ID precipitin lines formed between a crude antigen preparation and antiserum against whole virus.
从感染山羊关节炎-脑炎病毒(CAEV)的山羊血清与聚乙二醇浓缩培养基中的放射性标记病毒蛋白之间形成的沉淀线,从免疫扩散(ID)板上切下,并通过聚丙烯酰胺凝胶电泳进行分析。两条主要的沉淀线包含135000摩尔质量的糖蛋白(gp135)和内部28000摩尔质量的结构蛋白(p28)。这种方法避免了使用纯化蛋白或单特异性抗血清来明确确定在粗抗原制剂和抗全病毒血清之间形成的ID沉淀线中的病毒成分。