BD PharmingenTM Alexa Fluor 647 Mouse Anti-Human Leptin Receptor (CD295)

Description

Multicolor flow cytometric analysis of Leptin Receptor CD295 on human mononuclear cells. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. The leucocytes were washed and stained with FITC Mouse Anti-Human CD14 Cat No. 555397/557153/561712 , BD Horizon V450 Mouse Anti-Human CD19 Cat No. 644491 antibodies and either Alexa Fluor 647 Mouse IgG2b, kappa Isotype Control Cat No. 557903 or Alexa Fluor 647 Mouse Anti-Human Leptin Receptor CD295 antibody Cat No. 564376 . The flow cytometric dot plots show the correlated expression patterns of CD19 Upper Panels or CD14 Lower Panels versus Leptin Receptor CD295 or Ig Isotype control staining for gated events with the forward and side light-scatter characteristics of viable mononuclear leucocytes. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Multicolor flow cytometric analysis of Leptin Receptor CD295 on human mononuclear cells. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. The leucocytes were washed and stained with FITC Mouse Anti-Human CD14 Cat No. 555397/557153/561712 , BD Horizon V450 Mouse Anti-Human CD19 Cat No. 644491 antibodies and either Alexa Fluor 647 Mouse IgG2b, kappa Isotype Control Cat No. 557903 or Alexa Fluor 647 Mouse Anti-Human Leptin Receptor CD295 antibody Cat No. 564376 . The flow cytometric dot plots show the correlated expression patterns of CD19 Upper Panels or CD14 Lower Panels versus Leptin Receptor CD295 or Ig Isotype control staining for gated events with the forward and side light-scatter characteristics of viable mononuclear leucocytes. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Multicolor flow cytometric analysis of Leptin Receptor CD295 on human mononuclear cells. Human peripheral blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to lyse erythrocytes. The leucocytes were washed and stained with FITC Mouse Anti-Human CD14 Cat No. 555397/557153/561712 , BD Horizon V450 Mouse Anti-Human CD19 Cat No. 644491 antibodies and either Alexa Fluor 647 Mouse IgG2b, kappa Isotype Control Cat No. 557903 or Alexa Fluor 647 Mouse Anti-Human Leptin Receptor CD295 antibody Cat No. 564376 . The flow cytometric dot plots show the correlated expression patterns of CD19 Upper Panels or CD14 Lower Panels versus Leptin Receptor CD295 or Ig Isotype control staining for gated events with the forward and side light-scatter characteristics of viable mononuclear leucocytes. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System.