BD HorizonTM BV786 Rat Anti-Mouse CD105

Description

Flow cytometric analysis of CD105 expressed on mouse bEnd.3 cells. Cells from the mouse bEnd.3 Endothelioma, ATCC CRL-2299 cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV786 Rat IgG2a, kappa Isotype Control Cat. No. 563335; dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD105 antibody Cat. No. 564746, solid line histogram . The fluorescence histogram showing CD105 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bEnd.3 cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD105 expressed on mouse bEnd.3 cells. Cells from the mouse bEnd.3 Endothelioma, ATCC CRL-2299 cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV786 Rat IgG2a, kappa Isotype Control Cat. No. 563335; dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD105 antibody Cat. No. 564746, solid line histogram . The fluorescence histogram showing CD105 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bEnd.3 cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD105 expressed on mouse bEnd.3 cells. Cells from the mouse bEnd.3 Endothelioma, ATCC CRL-2299 cell line were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either BD Horizon BV786 Rat IgG2a, kappa Isotype Control Cat. No. 563335; dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD105 antibody Cat. No. 564746, solid line histogram . The fluorescence histogram showing CD105 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bEnd.3 cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.