Influence of RBCs and platelet concentration on tail bleeding time. For the hemolytic anemia model, mice were evaluated 24 hours after being treated with PHZ (n = 13) or an equal volume of buffer control (n = 15) for hematocrit (A), platelet count (B), reticulated platelet percentage (C), and tail bleeding time (D) (t test). For the ITP model, mice were evaluated for hematocrit (E), platelet count (F), and tail bleeding time (G) 3 hours after IV injection of a monoclonal (n = 6) or polyclonal (n = 10) anti-GP1bα antibody (1-way ANOVA).
Figure 2.

Influence of RBCs and platelet concentration on tail bleeding time. For the hemolytic anemia model, mice were evaluated 24 hours after being treated with PHZ (n = 13) or an equal volume of buffer control (n = 15) for hematocrit (A), platelet count (B), reticulated platelet percentage (C), and tail bleeding time (D) (t test). For the ITP model, mice were evaluated for hematocrit (E), platelet count (F), and tail bleeding time (G) 3 hours after IV injection of a monoclonal (n = 6) or polyclonal (n = 10) anti-GP1bα antibody (1-way ANOVA).

This Feature Is Available To Subscribers Only

or Create an Account

Close Modal
Close Modal