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Abstract:
Highly purified native preparation of adhesion factor (AF) from rat liver was shown to inactivate after dialysis against deionised water or after action of chelating agent (EGTA). Isoelectric point of inactivated AF was less than 2.0 Rf value in PAG in presence of SDS was significantly increased. The results obtained suggest that inactivation of AF during electrofucusing depends on ampholyne binding of Ca(II) which may be constituent in AF.