Figure 1
Figure 1. IP6K1 is expressed in platelets and megakaryocytes. (A) Western blot analysis of lysates prepared from WT and Ip6k1−/− platelets pooled from 3 mice of each genotype, using an antibody against IP6K1. GAPDH was used as a loading control. The blot is representative of 3 independent experiments. (B) Immunohistofluorescence analysis of IP6K1 expression (green) in femur bone marrow sections. Nuclei are counterstained with propidium iodide (red). Images were acquired by confocal microscopy (LSM 510 META; Carl Zeiss) using a 63×/1.4NA objective (Carl Zeiss). To improve visualization of IP6K1 staining (green), images were subjected to a 10% linear increase in brightness using LSM Browser (Carl Zeiss), and nonlinear adjustment of contrast and tonal range using Adobe Photoshop (level adjustment). Scale bars represent 10 µm.

IP6K1 is expressed in platelets and megakaryocytes. (A) Western blot analysis of lysates prepared from WT and Ip6k1−/− platelets pooled from 3 mice of each genotype, using an antibody against IP6K1. GAPDH was used as a loading control. The blot is representative of 3 independent experiments. (B) Immunohistofluorescence analysis of IP6K1 expression (green) in femur bone marrow sections. Nuclei are counterstained with propidium iodide (red). Images were acquired by confocal microscopy (LSM 510 META; Carl Zeiss) using a 63×/1.4NA objective (Carl Zeiss). To improve visualization of IP6K1 staining (green), images were subjected to a 10% linear increase in brightness using LSM Browser (Carl Zeiss), and nonlinear adjustment of contrast and tonal range using Adobe Photoshop (level adjustment). Scale bars represent 10 µm.

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