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As a global market leader with numerous subsidiaries and distributors, Miltenyi Biotec is committed to providing our customers around the world with the highest quality products. In addition to direct selling in more than 20 countries in North America, Europe and Asia/Pacific, Miltenyi Biotec also provides support for our customers through an extensive distributor network covering dozens of additional countries.
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Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Clone | REA1039 |
---|---|
Clonality | monoclonal |
Isotype | recombinant human IgG1 |
Isotype control | REA Control Antibody (I), human IgG1 |
Host | cell line |
Type of antibody | Primary antibodies, Recombinant antibodies |
Species | human |
Antigen | IL-21 |
Alternative names of antigen | CVID11, Za11 |
Molecular mass of antigen [kDa] | 15 |
Distribution of antigen | T cells, CD4+ T cells, T helper cells, Tfh cells |
Entrez Gene ID | 59067 |
RRID | AB_2727992, AB_2727941, AB_2727993, AB_2727942, AB_2727994, AB_2727943 |
Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. | Figure 1Human peripheral blood mononuclear cells (PBMCs) were either left unstimulated (left images) or stimulated with 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 µg/mL ionomycin for 6 hours. After two hours 1 µg/mL brefeldin A was added. Cells were then fixed, permeabilized, and stained with Anti-IL-21 antibodies as well as with CD154 and CD4 antibodies. CD4 + cells were pre-gated for the analysis. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris were excluded from the analysis based on scatter signals. |
Clone | REA1039 |
---|---|
Clonality | monoclonal |
Isotype | recombinant human IgG1 |
Isotype control | REA Control Antibody (I), human IgG1 |
Host | cell line |
Type of antibody | Primary antibodies, Recombinant antibodies |
Species | human |
Antigen | IL-21 |
Alternative names of antigen | CVID11, Za11 |
Molecular mass of antigen [kDa] | 15 |
Distribution of antigen | T cells, CD4+ T cells, T helper cells, Tfh cells |
Entrez Gene ID | 59067 |
RRID | AB_2727992, AB_2727941, AB_2727993, AB_2727942, AB_2727994, AB_2727943 |
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