BD Pharmingen- Biotin Mouse Anti-Human CD120a_BD Pharmingen
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Flow cytometric analysis of expression of cell surface TNFRI by whole-lysed human blood. Whole human blood was stained with Biotin Mouse Anti-Human CD120a (Cat No. 550900) followed by PE Streptavidin (Cat. No. 554061). Red blood cells were subsequently lysed with Lysing Buffer (Cat No. 555899). Staining with the Biotin Mouse Anti-Human CD120a (filled histogram) is compared to staining obtained using the Biotin Mouse IgG2a, κ Isotype Control (Cat. No. 553455), (open histograms). Histograms in figure are gated on the lymphocyte (left panel), monocyte (middle panel) and granulocyte (right panel) populations based on the side and forward light scattering characteristics. Note: Certain human cell lines or cell types (e.g., neutrophils, monocytes) can first be treated with reagents that block receptors for the Fc regions of immunoglobulin to avoid nonspecific immunofluorescent staining mediated by Fc receptors (for example see Reference by Browning et. al.).
Flow cytometric analysis of expression of cell surface TNFRI by whole-lysed human blood. Whole human blood was stained with Biotin Mouse Anti-Human CD120a (Cat No. 550900) followed by PE Streptavidin (Cat. No. 554061). Red blood cells were subsequently lysed with Lysing Buffer (Cat No. 555899). Staining with the Biotin Mouse Anti-Human CD120a (filled histogram) is compared to staining obtained using the Biotin Mouse IgG2a, κ Isotype Control (Cat. No. 553455; open histograms). Histograms in figure are gated on the lymphocyte (left panel), monocyte (middle panel) and granulocyte (right panel) populations based on the side and forward light scattering characteristics. Note: Certain human cell lines or cell types (e.g., neutrophils, monocytes) can first be treated with reagents that block receptors for the Fc regions of immunoglobulin to avoid nonspecific immunofluorescent staining mediated by Fc receptors (for example see Reference by Browning et. al.).
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