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Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of human Endosialin (CD248) on human palatal mesenchyme cells. HEPM cells (ATTC, CRL-1486) were surface stained with either Alexa Fluor® 647 Mouse IgG1 κ Isotype Control (Cat No. 557714, dotted line histogram) or Alexa Fluor® 647 Mouse Anti-Human Endosialin (CD248) (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometry was performed using a BD FACSCanto™ II Flow Cytometer System.
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The B1/35 monoclonal antibody specifically binds to CD248 which is also known as Endosialin, Tumor endothelial marker 1 (TEM1), and CD164 sialomucin-like 1 (CD164L1). CD248 is a heavily glycosylated, single-pass type I transmembrane protein. CD248 belongs to the Group XIV C-Type lectin family that includes CD93 and CD141/thrombomodulin. It is expressed on pericytes and stromal fibroblasts. Although the exact functions of CD248 remain to be determined, its expression is associated with angiogenesis and lymphoid tissue organization during development, as well as, with postnatal inflammation and tumor development and growth.
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.