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For research use only.

Verified Samples Verified Samples in IHC: Human lung cancer
Dilution IHC 1:150-1:300
Isotype IgG
Host Rabbit
Reactivity Human
Applications IHC
Clonality Polyclonal
Immunogen Recombinant Mouse IL-17A protein expressed by E.coli
Abbre IL-17A
Synonyms CTLA8,  CTLA-8,  CTLA8 cytotoxic T-lymphocyte-associated serine esterase 8,  Cytotoxic T-lymphocyte-associated antigen 8,  IL17,  IL-17,  IL17A,  IL-17A,  IL-17A cytotoxic T-lymphocyte-associated protein 8,  interleukin-17A,  interleukin 17 (cytotoxic T-lymphocyte-associated serine esterase 8),  interleukin 17A
Swissprot
Cellular Localization Secreted
Tissue Specificity Expressed by Th17 cell lineage(at protein level). Expressed in innate lymphoid cells(at protein level).Expressed in gamma-delta T cell subsets(at protein level).Expressed in iNKT cells(at protein level).
Concentration 1 mg/mL
Buffer PBS with 0.05% proclin 300, 1% protective protein and 50% glycerol,pH7.4
Purification Method Antigen Affinity Purification
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
background Interleukin-17A (IL-17A), also known as CTLA-8, is a 15-20 kDa glycosylated cytokine that plays an important role in anti-microbial and chronic inflammation. The six IL-17 cytokines (IL-17A-F)are encoded by separate genes but adopt a conserved cystine knot fold. Mature rat IL-17A shares 60% and 89% amino acid sequence identity with human and mouse IL-17A, respectively. IL-17A is secreted by Th17 cells, gamma /δ T cells, iNKT cells, NK cells, LTi cells, neutrophils, and intestinal Paneth cells. It forms disulfide-linked homodimers as well as disulfide-linked heterodimers with IL-17F. IL-17A exerts its effects through the transmembrane IL-17RA in complex with IL-17RC or IL-17RD. Both IL-17RA and IL-17RC are required for responsiveness to heterodimeric IL-17A/F. IL-17A promotes protective mucosal and epidermal inflammation in response to microbial infection. It induces chemokine production, neutrophil influx, and the production of antibacterial peptides. IL-17A/F likewise induces neutrophil migration, but IL-17F does not. IL-17A additionally enhances the production of inflammatory mediators by rheumatoid synovial fibroblasts and contributes to TNF-alpha induced shock. In contrast, it can protect against the progression of colitis by limiting chronic inflammation. IL-17A encourages the formation of autoreactive germinal centers and exacerbates the onset and progression of experimental models of autoimmunity. IL-17A has been shown to exert either tumorigenic or anti-tumor effects.
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Unconjugated

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