
562152 ·
BDB Bioscience · Cat: 562152
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD183 CXCR3 expression on C57BL/6 mouse splenocytes. Spleen cells were stained with APC Rat Anti-Mouse CD62L Cat. No. 553152 and with either PE Hamster IgG1 kappa Isotype Control Hamster IgG1, Cat. No. 553972; Left Panel or PE Hamster Anti-Mouse CD183 Cat. No. 562152; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric dot plots show the correlated expression patterns of CD62L versus CD183/CXCR3 or Ig isotype control staining for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.