Abstract
A peroxidase specific zymogram staining procedure has been designed which not only locates peroxidase isozymes which have been resolved electrophoretically, but simultaneously estimates the relative activity of each peroxidase isozyme in the system under study. This quantitative assay of individual peroxidase isozymes is chronometric; the time required for the appearance of a peroxidase band is inversely proportional to its activity. By recording the time required for the appearance of each peroxidase isozyme in a tissue extract, the percent contribution each isozyme makes toward the total peroxidatic activity of that tissue can readily be determined.
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