Figure 4.
Compared with F13a+/+clots, F13a+/−clots have delayed FXIII activation and fibrin crosslinking. PRP was clotted with TF/CaCl2 and quenched at the indicated time points. FXIII activation (generation of FXIII-A′) and fibrin crosslinking were analyzed by SDS-PAGE with western blotting. (A) Representative western blots and (B) quantitation of FXIII-A′ over time for clot formation in F13a+/+ and F13a+/− PRP. Data show mean ± SEM (n = 3-5). (C-D) Representative western blots for fibrin crosslinking in F13a+/+and F13a+/− PRP clots. (E-F) Quantification of γ-γ (E) and HMW (F) crosslinked fibrin species formation. Data show mean ± SEMs (n = 3-5). A.F.U., arbitrary fluorescence units.

Compared with F13a+/+clots, F13a+/−clots have delayed FXIII activation and fibrin crosslinking. PRP was clotted with TF/CaCl2 and quenched at the indicated time points. FXIII activation (generation of FXIII-A′) and fibrin crosslinking were analyzed by SDS-PAGE with western blotting. (A) Representative western blots and (B) quantitation of FXIII-A′ over time for clot formation in F13a+/+ and F13a+/− PRP. Data show mean ± SEM (n = 3-5). (C-D) Representative western blots for fibrin crosslinking in F13a+/+and F13a+/− PRP clots. (E-F) Quantification of γ-γ (E) and HMW (F) crosslinked fibrin species formation. Data show mean ± SEMs (n = 3-5). A.F.U., arbitrary fluorescence units.

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