Figure 6.
Figure 6. Efficient protein ablation, similar platelet phenotypes, but no altered lymphocyte counts in Csk;Gp1ba-Cre mice. (A) Protein levels of Csk and GAPDH in platelet lysates of the indicated genotypes were determined by capillary-based immunoassays with the respective antibodies. Platelet Csk protein levels were determined by normalizing Csk peak areas by GAPDH peak areas (Csk/GAPDH ratio), n = 3 to 6 mice per genotype. (B) Platelet counts and platelet volumes, n = 7 to 10 mice per genotype. (C) Platelet surface receptor expression of GPVI and G6b-B were measured by flow cytometry and shown as MFI, n = 6 to 10 mice per genotype. (D) White blood cell and lymphocyte counts, n = 9 to 33 mice per genotype. (A-D) Asterisks refer to significant difference in Cskfl/fl;Gp1ba-Cre+/KI or Cskfl/fl;Pf4-Cre+/KI mice compared with Csk+/+;Gp1ba-Cre+/KI or Csk+/+;Pf4-Cre+/KI mice, respectively (***P < .001; 1-way ANOVA with Sidak’s test); data represent mean ± SD.

Efficient protein ablation, similar platelet phenotypes, but no altered lymphocyte counts in Csk;Gp1ba-Cre mice. (A) Protein levels of Csk and GAPDH in platelet lysates of the indicated genotypes were determined by capillary-based immunoassays with the respective antibodies. Platelet Csk protein levels were determined by normalizing Csk peak areas by GAPDH peak areas (Csk/GAPDH ratio), n = 3 to 6 mice per genotype. (B) Platelet counts and platelet volumes, n = 7 to 10 mice per genotype. (C) Platelet surface receptor expression of GPVI and G6b-B were measured by flow cytometry and shown as MFI, n = 6 to 10 mice per genotype. (D) White blood cell and lymphocyte counts, n = 9 to 33 mice per genotype. (A-D) Asterisks refer to significant difference in Cskfl/fl;Gp1ba-Cre+/KI or Cskfl/fl;Pf4-Cre+/KI mice compared with Csk+/+;Gp1ba-Cre+/KI or Csk+/+;Pf4-Cre+/KI mice, respectively (***P < .001; 1-way ANOVA with Sidak’s test); data represent mean ± SD.

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