BD Pharmingen- Biotin Mouse Anti-Human CD59_BD Pharmingen
参考图片
Flow cytometric analysis of glycosylphosphatidylinositol (GPI) anchor protein on GPI defective mutant cells. GPI defective mutant cells were stained with Biotin Mouse Anti-Human CD59 (Cat. No. 555762; solid line histogram) or Biotin Mouse IgG2a, κ Isotype Control (Cat. No. 555572; dashed line histogram), and PE Streptavidin (Cat. No. 554061). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable cells. Flow cytometry was performed on a BD FACScan™.
Flow cytometric analysis of glycosylphosphatidylinositol (GPI) anchor protein on GPI defective mutant cells. GPI defective mutant cells were stained with Biotin Mouse Anti-Human CD59 (Cat. No. 555762; solid line histogram) or Biotin Mouse IgG2a, κ Isotype Control (Cat. No. 555572; dashed line histogram), and PE Streptavidin (Cat. No. 554061). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable cells. Flow cytometry was performed on a BD FACScan™.
Flow cytometric analysis of glycosylphosphatidylinositol (GPI) anchor protein cells on K562 cells. K562 cells were stained with Biotin Mouse Anti-Human CD59 (Cat. No. 555762; solid line histogram) or Biotin Mouse IgG2a, κ Isotype Control (Cat. No. 555572; dashed line histogram) and PE Streptavidin (Cat. No. 554061). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable cells. Flow cytometry was performed on a BD FACScan™.
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