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Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Flow cytometric analysis of PE-conjugated anti-mouse CD125 on mouse bone marrow cells. Isolated murine bone marrow cells were stained with either PE anti-CD125 (clone T21, Cat. No. 558488, right panel) or a PE-conjugated rat IgG1 isotype control (Cat. No. 557078, left panel) and FITC anti-CD11b (clone M1/70, Cat. No. 553310). Flow cytometry was performed on a BD FACSCalibur™ System and the histograms were derived from the gated events based on light scattering characteristics of viable bone marrow cells.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
For flow cytometry of cell suspensions from peripheral lymphoid tissues, it is recommended that the cells be pre-incubated with Mouse BD Fc Block™ Purified anti-Mouse CD16/CD32 mAb, Clone 2.4G2 (Cat. No. 553141/553142).
The T21 monoclonal antibody specifically binds to CD125 which is also known as the alpha subunit of the IL-5 Receptor (IL5RA/IL-5Rα). CD125 is a type I transmembrane protein that belongs to the hemopoietin receptor and Ig gene superfamilies. It is expressed on B cells and eosinophils. CD125 associates with the Common β chain (βc/Bc) subunit, also known as CD131, to form the functional IL-5 Receptor complex. Mouse IL-5 belongs to the hematopoietic growth factor family of cytokines and promotes the growth and differentiation of B cells and eosinophils. Upon binding, the T21 antibody blocks IL-5 binding to its receptor and can inhibit IL-5 induced B-cell proliferation and antibody production.
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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.
Comparisons, where applicable, are made against older BD technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.