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GENERAL CATALOGUE

BD PharmingenTM PE Mouse Anti-Human CD109

556040 ·

BDB Bioscience · Cat: 556040

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Catalog No: 556040
Category: reagents
Brand: BDB Bioscience

Description

Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system. Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system. Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system. Show More Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system. Show More Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system. Flow cytometric analysis of CD109 expression on human peripheral blood monocytes Left Panel and granulocytes Right Panel . Human whole blood was stained with PE Mouse Anti-Human CD109 Cat. No. 556040; solid line histogram or with PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; dashed line histogram . 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 viable monocytes or granulocytes. Flow cytometry was carried out on a BD FACSCan system.

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