BD PharmingenTM PE Rat Anti-Mouse CD192 (CCR2)

Description

Multicolor flow cytometric analysis of CD192 CCR2 expression on mouse splenocytes. C57BL/6 Top Plots and BALB/c Bottom Plots mouse spleen cells were treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with APC Rat Anti-Mouse Ly-6G and Ly-6C antibody Cat No. 553129/561083 , and either PE Rat IgG1, k Isotype Control Cat. No. 553925; Left Panels or PE Rat Anti-Mouse CD192 CCR2 antibody Cat. No. 568093; Right Plots at 0.5 mug/test. DAPI 4,6-Diamidino-2-Phenylindole, Dihydrochloride Solution Cat. No. 564907 was added to cells right before analysis. Bivariate pseudocolor density plots showing the correlated expression of CD192 CCR2 or Ig Isotype control staining versus Ly-6G and Ly-6C were derived from gated events with the forward and side light-scattering characteristics of viable DAPI-negative leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Multicolor flow cytometric analysis of CD192 CCR2 expression on mouse splenocytes. C57BL/6 Top Plots and BALB/c Bottom Plots mouse spleen cells were treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with APC Rat Anti-Mouse Ly-6G and Ly-6C antibody Cat No. 553129/561083 , and either PE Rat IgG1, k Isotype Control Cat. No. 553925; Left Panels or PE Rat Anti-Mouse CD192 CCR2 antibody Cat. No. 568093; Right Plots at 0.5 mug/test. DAPI 4,6-Diamidino-2-Phenylindole, Dihydrochloride Solution Cat. No. 564907 was added to cells right before analysis. Bivariate pseudocolor density plots showing the correlated expression of CD192 CCR2 or Ig Isotype control staining versus Ly-6G and Ly-6C were derived from gated events with the forward and side light-scattering characteristics of viable DAPI-negative leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Multicolor flow cytometric analysis of CD192 CCR2 expression on mouse splenocytes. C57BL/6 Top Plots and BALB/c Bottom Plots mouse spleen cells were treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes, washed, and preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with APC Rat Anti-Mouse Ly-6G and Ly-6C antibody Cat No. 553129/561083 , and either PE Rat IgG1, k Isotype Control Cat. No. 553925; Left Panels or PE Rat Anti-Mouse CD192 CCR2 antibody Cat. No. 568093; Right Plots at 0.5 mug/test. DAPI 4,6-Diamidino-2-Phenylindole, Dihydrochloride Solution Cat. No. 564907 was added to cells right before analysis. Bivariate pseudocolor density plots showing the correlated expression of CD192 CCR2 or Ig Isotype control staining versus Ly-6G and Ly-6C were derived from gated events with the forward and side light-scattering characteristics of viable DAPI-negative leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific.