Author:
Zolton Raymond P.,Mertz Edwin T.
Abstract
Highly purified sheep, bovine, and human plasminogen can be prepared by affinity chromatography of the plasma or plasma euglobulin fraction on a column of Sepharose–Butesin (Sepharose–NH∙C6H4∙COOC4-H9). Since plasma is not bound, the column can also be used to monitor the conversion of plasminogen to plasmin.
Publisher
Canadian Science Publishing
Cited by
9 articles.
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