BD Pharmingen- FITC Mouse Anti-Human CD59_BD Pharmingen
参考图片
Flow cytometric analysis of CD59 expression on human glycosylphosphatidiylinositol (GPI) anchor -defective cell line (left panel) or K562 cells expressing GPI anchor protein (right panel). Whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 555573; dashed line histograms) or FITC Mouse Anti-Human CD59 antibody (Cat. No. 555763/560954; solid line histograms). Erythrocytes were lysed with BD FACS Lysing Solution (Cat. No. 349202). Fluorescent histograms depicting CD59 (or Ig isotype control) staining were derived from gated events with the forward and side-light scatter characteristics of K562 cells. Flow cytometric analysis was performed using a BD FACScan™ Cytometer System.
Flow cytometric analysis of CD59 expression on human glycosylphosphatidiylinositol (GPI) anchor -defective cell line (left panel) or K562 cells expressing GPI anchor protein (right panel). Whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 555573; dashed line histograms) or FITC Mouse Anti-Human CD59 antibody (Cat. No. 555763/560954; solid line histograms). Erythrocytes were lysed with BD FACS Lysing Solution (Cat. No. 349202). Fluorescent histograms depicting CD59 (or Ig isotype control) staining were derived from gated events with the forward and side-light scatter characteristics of K562 cells. Flow cytometric analysis was performed using a BD FACScan™ Cytometer System.
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