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The protein encoded by IL22 is a cytokine that shares the sequence similarity with IL17. Additionally we are shipping Interleukin 22 Kits (77) and Interleukin 22 Proteins (76) and many more products for this protein.
Showing 10 out of 281 products:
Human Polyclonal IL22 Primary Antibody for Func, FACS - ABIN2665496
Gu, Yang, Ouyang, Liu, Li, Yang, Bromberg, Chen, Mayer, Unkeless, Xiong: Interleukin 10 suppresses Th17 cytokines secreted by macrophages and T cells. in European journal of immunology 2008
Show all 8 references for ABIN2665496
Human Polyclonal IL22 Primary Antibody for FACS - ABIN2661327
Trifari, Kaplan, Tran, Crellin, Spits: Identification of a human helper T cell population that has abundant production of interleukin 22 and is distinct from T(H)-17, T(H)1 and T(H)2 cells. in Nature immunology 2009
Show all 8 references for ABIN2661327
Mouse (Murine) Polyclonal IL22 Primary Antibody for FACS - ABIN2663784
Martin, Hirota, Cua, Stockinger, Veldhoen: Interleukin-17-producing gammadelta T cells selectively expand in response to pathogen products and environmental signals. in Immunity 2009
Show all 7 references for ABIN2663784
Mouse (Murine) Polyclonal IL22 Primary Antibody for FACS - ABIN2657957
Wolk, Witte, Hoffmann, Doecke, Endesfelder, Asadullah, Sterry, Volk, Wittig, Sabat: IL-22 induces lipopolysaccharide-binding protein in hepatocytes: a potential systemic role of IL-22 in Crohn's disease. in Journal of immunology (Baltimore, Md. : 1950) 2007
Show all 6 references for ABIN2657957
Mouse (Murine) Polyclonal IL22 Primary Antibody for FACS - ABIN2660208
Dumoutier, Louahed, Renauld: Cloning and characterization of IL-10-related T cell-derived inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9. in Journal of immunology (Baltimore, Md. : 1950) 2000
Show all 6 references for ABIN2660208
Mouse (Murine) Polyclonal IL22 Primary Antibody for FACS - ABIN2658347
Veldhoen, Hirota, Christensen, OGarra, Stockinger: Natural agonists for aryl hydrocarbon receptor in culture medium are essential for optimal differentiation of Th17 T cells. in The Journal of experimental medicine 2009
Show all 6 references for ABIN2658347
Human Polyclonal IL22 Primary Antibody for IHC (p), IHC - ABIN152152
Kato-Kogoe, Nishioka, Kawabe, Kataoka, Yamanegi, Yamada, Hata, Yamamoto, Nakasho, Urade, Terada, Ohyama: The promotional effect of IL-22 on mineralization activity of periodontal ligament cells. in Cytokine 2012
Show all 2 references for ABIN152152
Human Polyclonal IL22 Primary Antibody for IF (p), IHC (p) - ABIN748163
Huang, Cao, Jiang, Zhang, Gao: Th22 cell accumulation is associated with colorectal cancer development. in World journal of gastroenterology : WJG 2015
Human Polyclonal IL22 Primary Antibody for WB - ABIN657953
Meng, Gui, Xu, Lu, Jiao, Fan, Ge, Ke, Zhang, Wu, Wang: Association of Shp2 with phosphorylated IL-22R1 is required for interleukin-22-induced MAP kinase activation. in Journal of molecular cell biology 2010
Cow (Bovine) Polyclonal IL22 Primary Antibody for WB - ABIN2783788
Aujla, Chan, Zheng, Fei, Askew, Pociask, Reinhart, McAllister, Edeal, Gaus, Husain, Kreindler, Dubin, Pilewski, Myerburg, Mason, Iwakura, Kolls: IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia. in Nature medicine 2008
Expression analysis of IL-22, IL-26 (show IL26 Antibodies) and two IFN-gamma (show IFNG Antibodies) genes suggests an active role of these genes in immune responses in fish.
These findings provide new insights into the acetylcholine receptor (show CHRNA1 Antibodies)-mediated regulatory mechanism of SLURP-2 (show LYNX1 Antibodies) expression in keratinocytes.
TTP (show ADAMTS13 Antibodies)-dependent regulatory pathway described herein likely contributes to the role of IL-22 in inflammation and cancer and may evolve as novel target for pharmacological IL-22 modulation.
inflammatory cytokines, including IL-17 (show IL17A Antibodies) and IL-22, are expressed at higher levels by inflamed OA synovium and suggest IL-22 involvement in OA pathophysiology.
IL-17A (show IL17A Antibodies) and IL-22 work synergistically to induce antimicrobials and chemokines such as IL-8 (show IL8 Antibodies), components of calprotectin (show S100A8 Antibodies) (CP), lipocalin (show APOD Antibodies) (LCN) and some beta-defensins in both human and primary mouse gastric epithelial cells (GEC) and gastroids
The study demonstrated the probable involvement of gamma delta T cells in the immune response of an organism via the secretion of IL-17 (show IL17A Antibodies) and IL-22.
These results indicate that IL-22 is required for the proliferation of keratinocytes.
IL-17 (show IL17A Antibodies)- and IL-22-secreting myelin specific CD4 (show CD4 Antibodies)(+) T cells resistant to corticoids are associated with radiological activity of multiple sclerosis in early stages of the disease, mainly among Afrodescendant patients who, normally, have worse prognosis.
IL-22 induced at an early stage of L. monocytogenes infection enhances innate immunity against L. monocytogenes in the liver by stimulating hepatocytes to produce PLA2G2A (show PLA2G2A Antibodies)
IL-22/IFN-gamma (show IFNG Antibodies) producing T-cells were significantly increased in tumour tissue and that this increase was positively correlated with TNM (show ODZ1 Antibodies) staging of pancreatic ductal carcinoma and poorer patient survival.
High-glucose cultivation reduced IL-22 production in PBMCs that significantly reduced MMP-3 (show MMP3 Antibodies) expression and hampered migration of treated keratinocytes.
Rag-RORgammat-reporter and Rag KO mice undergoing ischemia reperfusion injury expressed high protein levels of both IL-22 and GFP (RORgammat)
Overexpression of IL-22 significantly reduced the Klebsiella pneumonia infection in the liver and spleen.
IL-22 restrains tapeworm-mediated protection against colitis via regulation of IL-25 (show IL25 Antibodies) expression
IL-22 is involved in plaque formation; IL-22 released by immune cells is involved in activation of vascular repair by stimulating medial SMC (show DYM Antibodies) dedifferentiation into a synthetic phenotype
cigarette smoke can inhibit the ROCK2 (show ROCK2 Antibodies)-IRF4 (show IRF4 Antibodies) axis and modulate T cell production of IL-22
IL-22 is not required for type 1 diabetes pathogenesis; suggested that IL-22 may have a regenerative and protective role in the pancreatic islets
IL-23 (show IL23A Antibodies), but not IL-17a (show IL17A Antibodies) or IL-22, promotes neutrophil recruitment and inflammatory cytokine and chemokine (show CCL1 Antibodies) expression in the colon in response to C. difficile infection.
Data suggest that interleukin 22 (IL-22) plays a pro-inflammatory/pathogenic role in the onset of antigen-induced arthritis (AIA) through apoptosis-associated speck-like Pycard (show PYCARD Antibodies) protein (ASC (show STS Antibodies))-dependent stimulation of interleukin-1 beta (IL-1beta (show IL1B Antibodies)) production.
SNPs in IFNG (show IFNG Antibodies), IFNGR1 (show IFNGR1 Antibodies) and R2, IL22, and IL22RA1 (show IL22RA1 Antibodies) were analyzed for an association to Estimated breeding values for somatic cell score in Canadian Holstein bulls; no significant associations were found.
Study concludes that bovine gamma/delta T cells are important sources of IL-22 and suggest a role for this cytokine in regulating immune responses at mucosal surfaces, including the gut (show GUSB Antibodies).
The protein encoded by this gene is a cytokine that shares the sequence similarity with IL17. The treatment of endothelial cells with this cytokine has been shown to stimulate the production of other cytokines including IL6, IL8 and CSF2/ GM-CSF. The increased expression of IL8 induced by this cytokine was found to be NF-kappa B-dependent.
, interleukin 27
, IL-10-related T-cell-derived inducible factor
, IL-10-related T-cell-derived-inducible factor
, cytokine Zcyto18
, IL-TIF alpha
, ILTIF alpha
, interleukin 10-related T cell-derived inducible factor