BD PharmingenTM Alexa Fluor 647 Mouse Anti-Human c-Met

Description

Flow cytometric analysis of human c-MET expression on MDA-MB-231 cells. Cells from the human MDA-MB-231 Breast adenocarcinoma, ATCC HTB-26 cell line were harvested with a trypsin-EDTA based cell dissociation buffer. The cells were then washed and stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human c-MET antibody Cat. No. 566014; solid line histogram . The histogram showing c-Met expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of human c-MET expression on MDA-MB-231 cells. Cells from the human MDA-MB-231 Breast adenocarcinoma, ATCC HTB-26 cell line were harvested with a trypsin-EDTA based cell dissociation buffer. The cells were then washed and stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human c-MET antibody Cat. No. 566014; solid line histogram . The histogram showing c-Met expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis of human c-MET expression on MDA-MB-231 cells. Cells from the human MDA-MB-231 Breast adenocarcinoma, ATCC HTB-26 cell line were harvested with a trypsin-EDTA based cell dissociation buffer. The cells were then washed and stained with either Alexa Fluor 647 Mouse IgG1, kappa Isotype Control Cat. No. 557714; dashed line histogram or Alexa Fluor 647 Mouse Anti-Human c-MET antibody Cat. No. 566014; solid line histogram . The histogram showing c-Met expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System.