
568784 · 25 Tests
BDB Bioscience · Cat: 568784
Reach 3+ verified distributors
Manufacturer product page
bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...
Description
Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of PD-L2 CD273 on Human monocyte-derived mature dendritic cells. Human monocyte-derived mature dendritic cells were stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or with PE Mouse Anti-human PD-L2 CD273 antibody Cat. No. 568783/568784; solid line histogram . The fluorescence histogram showing PD-L2 CD273 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry and data analysis were performed using a was performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software.