BD PharmingenTM PE Mouse Anti-Human CD49c (Integrin alpha3)

Description

Flow cytometric analysis of CD49c Integrin alpha3 expression on MG-63 cells. Cells from the human MG-63 Osteosarcoma, ATCC CRL-1427 cell line were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; solid line histogram . The fluorescent histogram showing CD49c Integrin alpha3 expression or Ig Isotype control staining was derived from gated events with the side and forward light-scattering events of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Multiparameter flow cytometric analysis of CD49c Integrin alpha3 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, k Isotype Control Cat. No. 554680; Left Plot or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing the correlated expression of CD49c Integrin alpha3 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Flow cytometric analysis of CD49c Integrin alpha3 expression on MG-63 cells. Cells from the human MG-63 Osteosarcoma, ATCC CRL-1427 cell line were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; solid line histogram . The fluorescent histogram showing CD49c Integrin alpha3 expression or Ig Isotype control staining was derived from gated events with the side and forward light-scattering events of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Multiparameter flow cytometric analysis of CD49c Integrin alpha3 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, k Isotype Control Cat. No. 554680; Left Plot or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing the correlated expression of CD49c Integrin alpha3 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of CD49c Integrin alpha3 expression on MG-63 cells. Cells from the human MG-63 Osteosarcoma, ATCC CRL-1427 cell line were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dashed line histogram or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; solid line histogram . The fluorescent histogram showing CD49c Integrin alpha3 expression or Ig Isotype control staining was derived from gated events with the side and forward light-scattering events of viable cells. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Multiparameter flow cytometric analysis of CD49c Integrin alpha3 expression on human peripheral blood leucocytes. Human whole blood was stained with either PE Mouse IgG1, k Isotype Control Cat. No. 554680; Left Plot or PE Mouse Anti-Human CD49c antibody Cat. No. 568718; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing the correlated expression of CD49c Integrin alpha3 or Ig Isotype control staining versus side light-scatter SSC-A signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software.