BD PharmingenTM PE Mouse Anti-Human CD66c

Description

Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Multivariate flow cytometric analysis of CD66c expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 555749; Left Plot or PE Mouse Anti-Human CD66c antibody Cat. No. 551478; Right Plot . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The bivariate pseudocolor density plot showing CD66c expression or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from events with the forward and side light-scatter characteristics of intact leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software.