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MACSQuant® Analyzer
Antibodies
navigationCytokine detection
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Biotec
for human cellsfor human cellsfor human cells
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for non-human primate cellsfor non-human primate cellsfor non-human primate cells
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Biotec
for mouse cellsfor mouse cellsfor mouse cells
Cytokine Secretion AssaysCytokine Secretion AssaysCytokine Secretion AssaysCytokine Secretion Assays
Cytokine detection antibodiesCytokine detection antibodiesCytokine detection antibodiesCytokine detection antibodies
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Biotec
Kits for cell detection and analysis
Tumor cell analysis
Immunofluorescent amplification (FASER Kits)
Inside Stain Kit
Staining of apoptotic and dead cells
Compensation reagents
Antibody biotinylation
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Anti-IL-17
Description
The Anti-IL-17 antibodies are designed for intracellular staining of IL-17A–producing cells.
Interleukin 17 (IL-17) is a family of cytokines that play a central role in adaptive immunity as well as autoinflammatory disorders.1 Data from several mouse models suggest that IL-17 plays a key role in the host defense against certain extracellular bacterial infections.
Recently, a new mouse T helper cell subset has been identified, which is dinstinct from Th1 and Th2 cells: IL-17–producing CD4+ T helper (Th17) cells. Th17 cells preferentially produce IL-17A, IL-17F, IL-21, and IL-22. Receptors for IL-17 and IL-22 are expressed on various epithelial tissues, thus Th17 cells are crucial for the cross-talk between immune system and tissues.2 It is now established that Th17 cells are responsible for driving autoimmune inflammation.
After stimulation of mouse T cells, IL-17 is not only secreted by CD4+ T cells, but also by CD8+ T cells and γδ T cells.
Applications
This Anti-IL-17 antibody has been developed for intracellular staining of IL-17 in fixed and permeabilized cells for flow cytometric analysis. Cells can be stained in suspension or by in-column intracellular staining technology in combination with MACS® Separation.
Clone Isotype
TC11-18H10Rat IgG1
 
Figure 1
Mouse spleen cells were incubated with or without PMA/ionomycin for 6 hours. After 2 hours brefeldin A was added. The cells were harvested, fixed, permeabilized, and intracellularly stained with Anti-IL-17-PE. Cell surface staining was performed with CD4-APC. Cells were analyzed by flow cytometry. B cells and cell debris were excluded from the analysis.
a: Stimulated sample
b: Unstimulated control
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Products
Anti-IL-17-FITC, mouse
- for 100 tests (1)
Download datasheet
130-094-298
Qty.:
 

Anti-IL-17-PE, mouse
- for 100 tests (1)
Download datasheet
130-094-296
Qty.:
 

Anti-IL-17-APC, mouse
- for 100 tests (1)
Download datasheet
130-094-294
Qty.:
 

(1) One test corresponds to fluorescent labeling of up to 107 cell in a total volume of 100 µL
Related products
Inside Stain Kit (#130-090-477)
Mouse IL-17 Secretion Assay – Cell Enrichment and Detection Kit (PE) (#130-094-213)
Mouse IL-17 Secretion Assay – Detection Kits
References
1. Weaver et al. (2007) Annu. Rev. Immunol. 25: 821–852.
2. Ouyang et al. (2008) Immunity 28: 454–467.
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