Figure 3.
Figure 3. Detection of GR in human platelets by flow cytometry and Western blotting analyses. (A) Washed platelets were permeabilized with saponin (“Materials and methods”) and stained with FITC-conjugated anti–P-selectin antibody or PE-conjugated anti-GR antibody. (Ai) Negative primary antibody control; (Aii) positive staining for GR; (Aiii) positive staining for P-selectin; and (Aiv) 2-color staining demonstrating dual positivity of platelets for P-selectin and GR (representative of data from 3 donors). (B) Human washed platelets and correspondent PBMC samples express GR; platelet GR has identical MW to PBMC GR. Blot is with samples from 3 distinct donors, and it is representative of 3 separate experiments.

Detection of GR in human platelets by flow cytometry and Western blotting analyses. (A) Washed platelets were permeabilized with saponin (“Materials and methods”) and stained with FITC-conjugated anti–P-selectin antibody or PE-conjugated anti-GR antibody. (Ai) Negative primary antibody control; (Aii) positive staining for GR; (Aiii) positive staining for P-selectin; and (Aiv) 2-color staining demonstrating dual positivity of platelets for P-selectin and GR (representative of data from 3 donors). (B) Human washed platelets and correspondent PBMC samples express GR; platelet GR has identical MW to PBMC GR. Blot is with samples from 3 distinct donors, and it is representative of 3 separate experiments.

Close Modal

or Create an Account

Close Modal
Close Modal