BD PharmingenTM PE Mouse Anti-Human MSR1 (CD204)

Description

Flow cytometric analysis of MSR1 CD204 expression on human monocyte-derived macrophages. Freshly isolated human monocytes were cultured 6 days with Recombinant Human GM-CSF protein Cat. No. 550068; 50 ng/ml . The cells were harvested with an enzyme-free cell dissociation solution, washed, and then stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human MSR1 CD204 antibody Cat. No. 566251; solid histogram . The histogram showing MSR1 CD204 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable macrophages. Flow cytometric analysis was performed using a BD Canto II Flow Cytometry System. Flow cytometric analysis of MSR1 CD204 expression on human monocyte-derived macrophages. Freshly isolated human monocytes were cultured 6 days with Recombinant Human GM-CSF protein Cat. No. 550068; 50 ng/ml . The cells were harvested with an enzyme-free cell dissociation solution, washed, and then stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human MSR1 CD204 antibody Cat. No. 566251; solid histogram . The histogram showing MSR1 CD204 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable macrophages. Flow cytometric analysis was performed using a BD Canto II Flow Cytometry System. Show More Flow cytometric analysis of MSR1 CD204 expression on human monocyte-derived macrophages. Freshly isolated human monocytes were cultured 6 days with Recombinant Human GM-CSF protein Cat. No. 550068; 50 ng/ml . The cells were harvested with an enzyme-free cell dissociation solution, washed, and then stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human MSR1 CD204 antibody Cat. No. 566251; solid histogram . The histogram showing MSR1 CD204 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable macrophages. Flow cytometric analysis was performed using a BD Canto II Flow Cytometry System.