
566653 ·
BDB Bioscience · Cat: 566653
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Show More Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Show More Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Multiparameter flow cytometric analysis of CCR2 CD192 expression on human leucocyte populations. Human peripheral blood cells were stained with either PE Mouse IgG2a, kappa Isotype Control Cat. No. 553457 or PE Anti-Human CCR2 CD192 antibody Cat. No. 566653 at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 .Two-parameter pseudocolor dot plots showing the correlated expression of CCR2 CD192 or Ig Isotype control staining versus side light-scatter SSC-A signals were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific.