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Multiparameter flow cytometric analysis of CD11b expression on mouse bone-marrow cells (Left and Centre Panels) or human peripheral granulocytes (Right Panel). BALB/c mouse bone-marrow cells and human whole blood were stained with either BD Horizon™ BV605 Rat IgG2b, κ Isotype Control (Cat. No. 563145; dashed line histograms) or BD Horizon™ BV605 Rat Anti-CD11b antibody (Cat. No. 563015; solid line histograms). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of lymphoid (ie, low-to-moderate side light-scatter-gated events, Left Panel), myeloid cells (ie, moderate-to-high side light-scatter-gated events, Centre Panel), or granulocytes (moderate-to-high side light-scatter-gated events, Right Panel). Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System.
Multiparameter flow cytometric analysis of CD11b expression on mouse bone-marrow cells (Left and Centre Panels) or human peripheral granulocytes (Right Panel). BALB/c mouse bone-marrow cells and human whole blood were stained with either BD Horizon™ BV605 Rat IgG2b, κ Isotype Control (Cat. No. 563145; dashed line histograms) or BD Horizon™ BV605 Rat Anti-CD11b antibody (Cat. No. 563015; solid line histograms). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of lymphoid (ie, low-to-moderate side light-scatter-gated events, Left Panel), myeloid cells (ie, moderate-to-high side light-scatter-gated events, Centre Panel), or granulocytes (moderate-to-high side light-scatter-gated events, Right Panel). Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System.