BD PharmingenTM PE Hamster Anti-Mouse Podoplanin

Description

Flow cytometric analysis of Podoplanin expressed on mouse C2C12 cells . Cells from the mouse C2C12 Myoblast, ATCC CRL-1772 cell line were harvested with trypsin-EDTA dissociation solution. The cells were then washed and stained with either PE Hamster IgG2, kappa Isotype Control Cat. No. 550085; dashed line histogram or PE Hamster Anti-Mouse Podoplanin antibody Cat. No. 566390; solid line histogram at 0.25 mug/ml. The histogram showing Podoplanin expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable C2C12 cells. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of Podoplanin expressed on mouse C2C12 cells . Cells from the mouse C2C12 Myoblast, ATCC CRL-1772 cell line were harvested with trypsin-EDTA dissociation solution. The cells were then washed and stained with either PE Hamster IgG2, kappa Isotype Control Cat. No. 550085; dashed line histogram or PE Hamster Anti-Mouse Podoplanin antibody Cat. No. 566390; solid line histogram at 0.25 mug/ml. The histogram showing Podoplanin expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable C2C12 cells. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of Podoplanin expressed on mouse C2C12 cells . Cells from the mouse C2C12 Myoblast, ATCC CRL-1772 cell line were harvested with trypsin-EDTA dissociation solution. The cells were then washed and stained with either PE Hamster IgG2, kappa Isotype Control Cat. No. 550085; dashed line histogram or PE Hamster Anti-Mouse Podoplanin antibody Cat. No. 566390; solid line histogram at 0.25 mug/ml. The histogram showing Podoplanin expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable C2C12 cells. Flow cytometric analysis was performed using a BD Canto II Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific.