Koblet H, Kohler U, Wyler R
Appl Microbiol. 1972 Sep;24(3):323-7. doi: 10.1128/am.24.3.323-327.1972.
The method for assaying chicken interferon by its inhibition of viral ribonucleic acid (RNA) synthesis was optimized for the chicken embryo fibroblast-Semliki Forest virus (SFV) system, with respect to time, multiplicity of infection, and addition of actinomycin D and (3)H-uridine. Incorporation of (3)H into viral RNA is reproducible, and amounts to 10(4) to 2 x 10(4) counts per min per uninhibited culture per 1 muCi per 6 hr. The assay may be carried out in less than 1 day and is sensitive (0.05 units/ml) and exact (+/-20% of the mean titers on different days); it can be used for purification procedures as well.
通过抑制病毒核糖核酸(RNA)合成来检测鸡干扰素的方法,针对鸡胚成纤维细胞 - 辛德毕斯病毒(SFV)系统,在时间、感染复数以及放线菌素D和(3)H - 尿苷的添加方面进行了优化。(3)H掺入病毒RNA的过程具有可重复性,每6小时每1微居里每未受抑制的培养物每分钟可达10⁴至2×10⁴计数。该检测可在不到1天的时间内完成,灵敏度高(0.05单位/毫升)且准确(不同日期平均滴度的±20%);它也可用于纯化程序。