Matheka H D, Coggins L, Shively J N, Norcross N L
Arch Virol. 1976;51(1-2):107-14. doi: 10.1007/BF01317839.
EIA virus was purified from equine fetal kidney cell cultures by PEG-precipitation, two sucrose-gradient sedimentations (5-30 per cent) and (25 to 60 per cent) centrifugation, using the immunodiffusion test to follow the procedure. Purified EIA virus had a density (20 degrees C) of 1.162 and a sedimentation constant of S20w=656. electron microscopy revealed a particle of about 100 nm in diameter with a very flexible but usually spherical shape. The dense core may be at various locations inside the membrane bound particle.
通过聚乙二醇沉淀、两次蔗糖梯度沉降(5%-30%和25%-60%)离心,从马胎儿肾细胞培养物中纯化马传染性贫血病毒(EIA病毒),并使用免疫扩散试验跟踪该过程。纯化后的EIA病毒在20℃时密度为1.162,沉降常数S20w = 656。电子显微镜显示,该病毒颗粒直径约100纳米,形状非常灵活,但通常呈球形。致密核心可能位于膜结合颗粒内的不同位置。