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Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of Alexa Fluor® 647 Mouse IgM, κ Isotype Control on blood lymphocytes. Whole blood was stained with Alexa Fluor® 647 Mouse IgM, κ Isotype Control (Cat. No. 560806; solid line histogram) or unstained (dashed line histogram). Erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). Fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD LSRII™.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Alexa Fluor® 647 Mouse IgM, κ Isotype Control is specific for the hapten trinitrophenol (TNP), a hapten not expressed on human or non-human primate primary cells or cell lines. In the absence of specific binding, this immunoglobulin may bind non-specifically to Fc receptors.
Please refer to Support Documents for Quality Certificates
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.