Fig. 4.
Fig. 4. Time course of factor XIIIa-catalyzed cross-linking. Cross-linking reactions with either fibrinogen-420 (upper panel) or fibrinogen-340 (lower panel) were carried out as described in “Materials and methods.” Lane 1 contains substrate alone. Lanes 2 to 6 contain substrate with either nonactivated factor XIII (lane 2) or thrombin-activated factor XIIIa (lanes 3-6), incubated for 2 minutes (lane 3), 5 minutes (lane 4), 30 minutes (lane 5), or 60 minutes (lane 6). Proteins were separated on homogenous 12% SDS-PAGE gels under reducing conditions and stained. Positions of individual and cross-linked fibrinogen chains are indicated. dαErefers to degraded αE, αE-xlinks refers to cross-linked αE chains, and α-xlinks refers to cross-linked α chains.

Time course of factor XIIIa-catalyzed cross-linking. Cross-linking reactions with either fibrinogen-420 (upper panel) or fibrinogen-340 (lower panel) were carried out as described in “Materials and methods.” Lane 1 contains substrate alone. Lanes 2 to 6 contain substrate with either nonactivated factor XIII (lane 2) or thrombin-activated factor XIIIa (lanes 3-6), incubated for 2 minutes (lane 3), 5 minutes (lane 4), 30 minutes (lane 5), or 60 minutes (lane 6). Proteins were separated on homogenous 12% SDS-PAGE gels under reducing conditions and stained. Positions of individual and cross-linked fibrinogen chains are indicated. dαErefers to degraded αE, αE-xlinks refers to cross-linked αE chains, and α-xlinks refers to cross-linked α chains.

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