Due to some routine maintenance you might experience temporary service interruptions or slowness on
Sunday, July 19, 2026, 2:00 - 10:00 am (EDT).
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Due to some routine maintenance you might experience temporary service interruptions or slowness on
Sunday, July 19, 2026, 2:00 - 10:00 am (EDT).
If you encounter problems while ordering, please contact us at BDBCustomerService@bd.com.
See MoreDue to some routine maintenance you might experience temporary service interruptions or slowness on
Sunday, July 19, 2026, 2:00 - 10:00 am (EDT)
.If you encounter problems while ordering, please contact us at BDBCustomerService@bd.com.
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Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with Alexa Fluor® 488 Mouse anti-Human CD19 antibody (Cat. No. 557697) and with either a PE-Cy™7 Mouse IgG2a, κ Isotype Control (Cat. No. 552868; Left Panel) or a PE-Cy™7 Mouse anti-Human IgD antibody (Cat. No. 561314; Right Panel). The two-color flow cytometric dot plots showing the correlated expression of IgD (or Ig isotype control staining) versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
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The IA6-2 monoclonal antibody specifically binds to the heavy chain of human Immunoglobulin D (IgD). IgD is a member of the immunoglobulin superfamily that exists in type 1-membrane (mIgD) and soluble glycoprotein forms. mIgD is expressed on mature naïve B cells (along with membrane IgM) and serves as a B-cell receptor for antigen (BCR). In response to antigen binding, the mIgD BCR, in association with other signaling molecules including CD79a and CD79b, can transduce activating or tolerizing signals intracellularly into B lymphocytes.
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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.