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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: J Thromb Haemost. 2012 Aug;10(8):1646–1652. doi: 10.1111/j.1538-7836.2012.04797.x

Fig. 1.

Fig. 1

Murine models of EC-VWF and Plt-VWF established by crossed BMT. (A) Plasma samples and (B) platelet lysates collected from WT, VWF−/−, EC-VWF, and Plt-VWF mice were analyzed by ELISAto measure VWF antigen levels. EC-VWF mice had WT levels of plasma VWF, but no platelet VWF. Plt-VWF mice had WT levels of platelet VWF and a trace amount of plasma VWF. (C) FVIII activity in mouse plasma was quantified by chromogenic assay. FVIII:C of EC-VWF mice were similar to WT mice. Plt-VWF mouse plasma presented low FVIII:C but the levels were significantly higher than VWF−/− mice. NS, not statistically significant, *P < 0.05