BD PharmingenTM PE Mouse Anti-Human Desmoglein 2

Description

Flow cytometric analysis of Desmoglein 2 expression on Human CD34+ lymphoid cells. Human peripheral blood mononuclear cells were stained with APC Mouse Anti-Human CD34 antibody Cat. No. 560940 and with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histogram showing Desmoglein 2 expression or Ig Isotype control staining Right Plot was derived from gated CD34 positive cells Left Plot as indicated with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of Desmoglein 2 expression on Human HeLa cells. Cells from the HeLa Cervical adenocarcinoma, ATCC CCL-2 cell line were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or with PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histograms showing the expression of Human Desmoglein 2 or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of Desmoglein 2 expression on Human CD34+ lymphoid cells. Human peripheral blood mononuclear cells were stained with APC Mouse Anti-Human CD34 antibody Cat. No. 560940 and with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histogram showing Desmoglein 2 expression or Ig Isotype control staining Right Plot was derived from gated CD34 positive cells Left Plot as indicated with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of Desmoglein 2 expression on Human HeLa cells. Cells from the HeLa Cervical adenocarcinoma, ATCC CCL-2 cell line were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or with PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histograms showing the expression of Human Desmoglein 2 or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of Desmoglein 2 expression on Human CD34+ lymphoid cells. Human peripheral blood mononuclear cells were stained with APC Mouse Anti-Human CD34 antibody Cat. No. 560940 and with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histogram showing Desmoglein 2 expression or Ig Isotype control staining Right Plot was derived from gated CD34 positive cells Left Plot as indicated with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of Desmoglein 2 expression on Human HeLa cells. Cells from the HeLa Cervical adenocarcinoma, ATCC CCL-2 cell line were stained with PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or with PE Mouse Anti-Human Desmoglein 2 antibody Cat. No. 568854/568855; solid line histogram . The fluorescence histograms showing the expression of Human Desmoglein 2 or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software.