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Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of human CD110 expression on platelets and HEL92.1.7 cells. Platelets (Left Panel) and HEL92.1.7 cells (Right Panel) were stained with either PE Mouse IgG2b Isotype Control (Cat. No. 555743; dashed line histogram) or PE Mouse anti-Human CD110 (Cat. No. 562159; solid line histogram). Flow cytometric fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of platelets or viable HEL92.1.7 cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
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The 1.6.1 monoclonal antibody specifically binds to the human Thrombopoietin Receptor (TPO-R) that is also known as the Myeloproliferative leukemia protein (c-Mpl) or CD110. CD110 is a type I transmembrane glycoprotein and a member of the hematopoietin receptor family. It is expressed on hematopoietic stem cells, a subfraction of hematopoietic precursor cells, cells of the megakaryocytic lineage and platelets. CD110 serves as a receptor for thrombopoietin. Upon binding of thrombopoietin to CD110, megakaryocyte proliferation and differentiation is induced, platelets are produced and stem cells are protected from apoptosis.
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