BD PharmingenTM Alexa Fluor 647 Mouse Anti-Sox9

Description

Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Show More Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System. Flow cytometric analysis of SOX9 expression in human hepatocellular carcinoma and embryonic stem cell lines. Hep G2 cells ATCC HB-8065, Left Panel and H9 cells WiCell, Madison, WI; Right Panel were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 , and permeabilized with BD Phosflow Perm Buffer III Cat. No. 558050 . The cells were stained with either Alexa Fluor 647 Mouse IgG1 kappa Isotype Control Cat. No.557732; dashed line histogram or Alexa Fluor 647 Mouse Anti-Sox9 Cat. No. 565493; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact Hep G2 or H9 cells, respectively. Flow cytometric analysis was performed using a BD FACSCanto II Flow Cytometer System.