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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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Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Anti-IL-6-PE staining control | Stimulated sample |
Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. | Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Anti-IL-6-APC staining control | Stimulated sample |
Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. | Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Clone | MP5-20F3 |
---|---|
Clonality | monoclonal |
Isotype | rat IgG1κ, rat IgG1 |
Isotype control | Isotype Control Antibody, rat IgG1 |
Host | rat |
Type of antibody | Primary antibodies, Functional-grade antibodies |
Species | mouse |
Antigen | IL-6 |
Molecular mass of antigen [kDa] | 22 |
Entrez Gene ID | 16193 |
RRID | AB_2660386, AB_2660387, AB_2660379 |
Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Anti-IL-6-PE staining control | Stimulated sample |
Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. | Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Anti-IL-6-APC staining control | Stimulated sample |
Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. | Figure 1Peritoneal cells were isolated from a BALB/c mouse injected with thioglycollate five days before. Adherent cells were stimulated with LPS for six hours. After two hours, brefeldin A was added. The cells were harvested and intracellularly stained with Anti-IL-6 and with CD115-APC or -PE. IL-6 staining controls (left images) were done by incubating cells with 100 μg/mL of Anti-IL-6 pure – functional grade antibody, prior to staining. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer. Gating was performed according to forward scatter and side scatter properties of the cells. |
Clone | MP5-20F3 |
---|---|
Clonality | monoclonal |
Isotype | rat IgG1κ, rat IgG1 |
Isotype control | Isotype Control Antibody, rat IgG1 |
Host | rat |
Type of antibody | Primary antibodies, Functional-grade antibodies |
Species | mouse |
Antigen | IL-6 |
Molecular mass of antigen [kDa] | 22 |
Entrez Gene ID | 16193 |
RRID | AB_2660386, AB_2660387, AB_2660379 |
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