Figure 6
Figure 6. Platelets from Unc13dJinx mice demonstrate a spreading defect. (A) Fluorescence microscopy of platelets from wild-type and Unc13dJinx mice spread for the indicated amounts of time on poly-L-lysine and stained with Alexa 546–phalloidin. Scale bars, 5 μm. (B) Quantification of surface area and perimeter in platelets from wild-type (solid circles, solid lines) and Unc13dJinx (open circles, dashed lines) mice spread on either poly-L-lysine, collagen, or fibronectin as indicated. Error bars represent the SEM of measurements from 150 to 250 platelets per time point.

Platelets from Unc13dJinx mice demonstrate a spreading defect. (A) Fluorescence microscopy of platelets from wild-type and Unc13dJinx mice spread for the indicated amounts of time on poly-L-lysine and stained with Alexa 546–phalloidin. Scale bars, 5 μm. (B) Quantification of surface area and perimeter in platelets from wild-type (solid circles, solid lines) and Unc13dJinx (open circles, dashed lines) mice spread on either poly-L-lysine, collagen, or fibronectin as indicated. Error bars represent the SEM of measurements from 150 to 250 platelets per time point.

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