BD PharmingenTM PE Mouse Anti-Human CD88 (C5a Receptor)

Description

Multiparameter flow cytometric analysis of CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo Software. Multiparameter flow cytometric analysis of CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo Software. Multiparameter flow cytometric analysis of CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. 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 CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. 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 CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo Software. Multiparameter flow cytometric analysis of CD88 C5a Receptor expression on Human peripheral blood leukocyte populations. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. After washing, the leukocytes were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 565363; Left Plot or PE Mouse Anti-Human CD88 C5a Receptor antibody Cat. No. 572176/572177; Right Plot . The bivariate pseudocolor density plot showing the correlated expression of CD88 C5a Receptor 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 intact leukocyte populations. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo Software.