BD Pharmingen- Purified Mouse P-Selectin - IgG Fusion Protein_BD Pharmingen
参考图片
Detection of P-Selectin ligands on mouse granulocytes (left panel) and mononuclear cells (right panel). BALB/c whole blood was stained with Mouse P-Selectin - IgG Fusion Protein followed by R-PE-conjugated goat anti-human IgG, Fcγ fragment specific (Jackson Immunoresearch, open histogram) or with the second-step alone (filled histogram). Erythrocytes were lysed (BD Pharm Lyse™ lysis buffer, Cat. No. 555899), non-viable leukocytes were excluded by staining with 7-AAD (BD Via-Probe™ cell viability dye, Cat. No. 555815/555816), and granulocytes and mononuclear cells were gated according to their light-scatter profiles. Flow cytometry was performed on a BD FACScan™ flow cytometry system.
Detection of P-Selectin ligands on mouse granulocytes (left panel) and mononuclear cells (right panel). BALB/c whole blood was stained with Mouse P-Selectin - IgG Fusion Protein followed by R-PE-conjugated goat anti-human IgG, Fcγ fragment specific (Jackson Immunoresearch, open histogram) or with the second-step alone (filled histogram). Erythrocytes were lysed (BD Pharm Lyse™ lysis buffer, Cat. No. 555899), non-viable leukocytes were excluded by staining with 7-AAD (BD Via-Probe™ cell viability dye, Cat. No. 555815/555816), and granulocytes and mononuclear cells were gated according to their light-scatter profiles. Flow cytometry was performed on a BD FACScan™ flow cytometry system.
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