Figure 1
tTF/tTF-NGR characterization. (A,B) SDS-PAGE and Western blot analysis of tTF and tTF-NGR. (C) Ability of the fusion proteins to enhance the specific proteolytic activation of FX by FVIIa in the presence of phospholipids was evaluated by Michaelis-Menten analysis as described by Ruf et al.22 The calculated Michaelis constants (Km) of the hyperbolic parts of the kinetic curves were 0.2 nM (tTF) and 0.4 nM (tTF-NGR), respectively. Mean values of 3-fold assays are given with SD.

tTF/tTF-NGR characterization. (A,B) SDS-PAGE and Western blot analysis of tTF and tTF-NGR. (C) Ability of the fusion proteins to enhance the specific proteolytic activation of FX by FVIIa in the presence of phospholipids was evaluated by Michaelis-Menten analysis as described by Ruf et al.22  The calculated Michaelis constants (Km) of the hyperbolic parts of the kinetic curves were 0.2 nM (tTF) and 0.4 nM (tTF-NGR), respectively. Mean values of 3-fold assays are given with SD.

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