Abstract
The fact that human Interferon is inactivated with protein as such as trypsin and pepsin has been noted, and a new method for quantitative determination was established. It was revealed that the decomposing substance of the human Interferon obtained by an action upon kallikrein or trypsin, under fixed conditions, hydrolyzed a substrate peptide MCA. By this method, a sensitive new method for quantitative determination of favorable reproducibility in human Interferon preparations and in human plasma was established.
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