McManus N H
Appl Environ Microbiol. 1976 Jan;31(1):35-8. doi: 10.1128/aem.31.1.35-38.1976.
This report describes an accurate, reproducible, and efficient microassay for human interferon, using a dye-uptake method to quantitate cytopathogenicity. The antiviral activity was measured by using a Gilford 300-N microsepctrophotometer, with the automatic programmer, sampler, and data lister. Two hundred interferon samples, each in a final volume of 1.0 ml, may be analyzed and recorded in 45 min. The reproducibility of a laboratory reference interferon and the human international reference B 69/19 on two different cell lines, using the model Q Oxford sampler, was found to be excellent, with the standard error of the log10 geometric mean of both references +/- 0.04 to 0.06.
本报告描述了一种准确、可重复且高效的人干扰素微量测定法,该方法采用染料摄取法对细胞致病性进行定量。抗病毒活性通过使用配备自动编程器、采样器和数据列表器的吉尔福德300 - N型微量分光光度计进行测量。200个干扰素样品,每个样品的终体积为1.0毫升,可在45分钟内进行分析和记录。使用牛津Q型采样器,在两种不同细胞系上对实验室参考干扰素和人国际参考品B 69/19的重复性进行检测,结果发现非常出色,两种参考品log10几何平均值的标准误差为±0.04至0.06。