BD PharmingenTM PE Rat Anti-Mouse CD98

Description

Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh Unstimulated; Left Panel or 48 hours after Con A mitogenic stimulation Stimulated; Right Panel . The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 and stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 553930; dotted line histogram or PE Rat Anti-Mouse CD98 antibody Cat No. 567949; solid line histogram at 0.125 mug/test. The fluorescence histograms showing CD98 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo software. Data shown on this Technical Data Sheet are not lot specific.