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Flow cytometric analysis of IFN-γ expression in stimulated human peripheral blood mononuclear cells. HiCK-1 Human Cytokine Positive Control Cells (Cat. No. 555061) were permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained with either Purified Mouse IgG1, κ Isotype Control (Cat No. 556648, Left Panel) or with the Purified Mouse Anti-Human IFN-γ antibody (Cat No. 554549, Right Panel), followed by FITC Goat Anti-Mouse Ig (Cat. No. 554001). Flow cytometric dot plots showing the expression of IFN-γ (or Ig Isotype Control staining) versus side scatter were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD FACSCanto™ System.
Flow cytometric analysis of IFN-γ expression in stimulated human peripheral blood mononuclear cells. HiCK-1 Human Cytokine Positive Control Cells (Cat. No. 555061) were permeabilized with BD Perm/Wash™ Buffer (Cat. No. 554723). The cells were then stained with either Purified Mouse IgG1, κ Isotype Control (Cat No. 556648, Left Panel) or with the Purified Mouse Anti-Human IFN-γ antibody (Cat No. 554549, Right Panel), followed by FITC Goat Anti-Mouse Ig (Cat. No. 554001). Flow cytometric dot plots showing the expression of IFN-γ (or Ig Isotype Control staining) versus side scatter were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD FACSCanto™ System.