BD PharmingenTM Alexa Fluor 647 Mouse Anti-Human Transferrin R (CD71)

Description

Flow cytometric analysis of Transferrin R CD71 expression on activated human peripheral blood mononuclear cells PBMC . Human PBMC were stimulated for 3 days with Phytohemagglutinin PHA . The cells were harvested, preincubated with Human BD Fc Block Cat. No. 564219/564220 , and then stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 565571; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human Transferrin R CD71 antibody Cat. No. 566724/566725; solid line histogram . BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histogram showing CD71 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable activated human peripheral mononuclear cells. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Flow cytometric analysis of Transferrin R CD71 expression on activated human peripheral blood mononuclear cells PBMC . Human PBMC were stimulated for 3 days with Phytohemagglutinin PHA . The cells were harvested, preincubated with Human BD Fc Block Cat. No. 564219/564220 , and then stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 565571; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human Transferrin R CD71 antibody Cat. No. 566724/566725; solid line histogram . BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histogram showing CD71 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable activated human peripheral mononuclear cells. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software. Show More Flow cytometric analysis of Transferrin R CD71 expression on activated human peripheral blood mononuclear cells PBMC . Human PBMC were stimulated for 3 days with Phytohemagglutinin PHA . The cells were harvested, preincubated with Human BD Fc Block Cat. No. 564219/564220 , and then stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 565571; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human Transferrin R CD71 antibody Cat. No. 566724/566725; solid line histogram . BD Via-Probe Cell Viability 7-AAD Solution Cat. No. 555815/555816 was added to cells right before analysis. The fluorescence histogram showing CD71 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable activated human peripheral mononuclear cells. Flow cytometry and data analysis were performed using a BD FACSCelesta Flow Cytometer System and FlowJo software.