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BD PharmingenTM Alexa Fluor 700 Mouse Anti-Human CD33

561160 ·

BDB Bioscience · Cat: 561160

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Catalog No: 561160
Category: reagents
Brand: BDB Bioscience

Description

Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD33 expression on human peripheral blood leukocytes. Whole blood was stained with FITC Mouse Anti-Human CD14 Cat. No. 555397 and Alexa Fluor 700 Mouse Anti-Human CD33 antibody Cat. No. 561160; solid line histogram or with a Alexa Fluor 700 Mouse IgG1, kappa Isotype Control Cat. No. 557882; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from CD14-positive monocytes Left Panel or CD14-negative granulocytes Right Panel with the light scattering properties of viable cells. Flow cytometry was performed using a BD LSR II Flow Cytometer System.

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