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The protein encoded by IL25 is a cytokine that shares sequence similarity with interleukin 17. Additionally we are shipping IL25 Proteins (61) and IL25 Kits (51) and many more products for this protein.
Showing 10 out of 225 products:
Human Polyclonal IL25 Primary Antibody for EIA, IHC (p) - ABIN952925
Xu, Zhang, Wang, Xu, Liu, Han, Wang, Zuo, Li: Opposing roles of IL-17A and IL-25 in the regulation of TSLP production in human nasal epithelial cells. in Allergy 2010
Show all 5 references for ABIN952925
Human Monoclonal IL25 Primary Antibody for FACS, WB - ABIN4900221
Corrigan, Wang, Meng, Fang, Wu, Reay, Lv, Fan, An, Wang, Liu, Lee, Ying: T-helper cell type 2 (Th2) memory T cell-potentiating cytokine IL-25 has the potential to promote angiogenesis in asthma. in Proceedings of the National Academy of Sciences of the United States of America 2011
Show all 4 references for ABIN4900221
Human Monoclonal IL25 Primary Antibody for IHC (p), IHC - ABIN252500
Terrier, Bièche, Maisonobe, Laurendeau, Rosenzwajg, Kahn, Diemert, Musset, Vidaud, Sène, Costedoat-Chalumeau, Le Thi-Huong, Amoura, Klatzmann, Cacoub, Saadoun: Interleukin-25: a cytokine linking eosinophils and adaptive immunity in Churg-Strauss syndrome. in Blood 2010
Show all 2 references for ABIN252500
Human Monoclonal IL25 Primary Antibody for FACS - ABIN4897387
Gironi, Saresella, Rovaris, Vaghi, Nemni, Clerici, Grossi: A novel data mining system points out hidden relationships between immunological markers in multiple sclerosis. in Immunity & ageing : I & A 2013
Show all 2 references for ABIN4897387
Human Monoclonal IL25 Primary Antibody for FACS, WB - ABIN1043795
Conti, Shen, Nayyar, Stocum, Sun, Lindemann, Ho, Hai, Yu, Jung, Filler, Masso-Welch, Edgerton, Gaffen: Th17 cells and IL-17 receptor signaling are essential for mucosal host defense against oral candidiasis. in The Journal of experimental medicine 2009
Findings indicate that the release of interleukin 25 (IL-25) from tumour-associated fibroblasts (TAFs) may serve as a check point for control of mammary tumour metastasis.
IL-25 and CD4(+) TH2 cells enhance type 2 innate lymphoid cell-derived IL-13 production, which promotes IgE-mediated experimental food allergy.
IL-22 (show IL22 Antibodies) restrains tapeworm-mediated protection against colitis via regulation of IL-25 expression
IL-25 promotes the function of CD4 (show CD4 Antibodies)+CD25 (show IL2RA Antibodies)+ T regulatory cells and prolongs skin-graft survival in murine models
IL-25 and IL-33 (show IL33 Antibodies) are critical for induction of Th2-type cytokine-mediated allergic airway eosinophilia, but not Th17-type cytokine-mediated airway neutrophilia, at the local sites of lungs in the challenge phase of mice sensitized EC with OVA
Suggest that chronic exposure of murine airways to IL-25 alone is able to reproduce a local angiogenic milieu in asthmatic mice.
we have demonstrated that the expression of ET-1 (show EDN1 Antibodies) and IL-25 was coordinately upregulated in the lesional keratinocytes of patients with AD and a murine AD model.
Colonic isolated lymphoid follicles develop in the absence of a number of factors required for the development of their small intestinal counterparts and can be specifically suppressed by factors other than IL-25.
These data demonstrate that dysregulated IL-25 expression contributes to lipid accumulation, whereas exogenous IL-25 protects against hepatic steatosis through IL-13 (show IL13 Antibodies) activation of STAT6 (show STAT6 Antibodies).
Concerted activity of IgG1 antibodies and IL-4 (show IL4 Antibodies)/IL-25-dependent effector cells trap helminth larvae in the tissues following vaccination with defined secreted antigens, providing sterile immunity to challenge infection.
Our findings suggest that the IL-25/IL-25R axis may play an important role in promoting the recruitment and proinflammatory function of eosinophils in allergic asthma.
Chronic rhinosinusitis with nasal polyps (CRSwNP) epithelial cells release TSLP (show TSLP Antibodies) and IL-25 when stimulated by poly(I:C) but not by DP or AF, suggesting that viral infection may contribute to maintain and amplify the T2 immune response seen in CRSwNP.
Increased induction and expression of TSLP (show TSLP Antibodies), IL-25, and IL-33 (show IL33 Antibodies) from nasal epithelial cells contribute to the pathophysiology of eosinophilic chronic rhinosinusitis.
Women with endometriosis showed significantly higher levels of IL-25 in their PF (p=0.019) compared to controls. IL-25 levels did not correlate with the stage of endometriosis.
IL-8 (show IL8 Antibodies) and IL-25 are targets of miR (show MLXIP Antibodies)-20b.
Our findings indicate that the alarmin cytokines IL-33 (show IL33 Antibodies) and IL-25 increase basophil activation and migratory potential, and may pose as a novel therapeutic targets for the treatment of allergic asthma.
The IL17E rs79877597 SNP was a modifier of the risk for psoriasis disease severity and psoriatic arthritis.
Therefore, IL-17E/IL-17RB signaling represents a potential therapeutic target for treatment of hepatocellular carcinoma
IL-25 upregulated PD-L1 (show CD274 Antibodies) surface expression through the signaling pathways of JNK (show MAPK8 Antibodies) and STAT3 (show STAT3 Antibodies), with STAT3 (show STAT3 Antibodies) found to constitutively occupy the proximal region of the PD-L1 (show CD274 Antibodies) promoter.
The protein encoded by this gene is a cytokine that shares sequence similarity with interleukin 17. This cytokine can induce NF-kappaB activation, and stimulate the production of interleukin 8. Both this cytokine and interleukin 17B are ligands for the cytokine receptor IL17BR. Studies of a similar gene in mice suggest that this cytokine may be a pro-inflammatory cytokine favoring the Th2-type immune response. Alternative splicing results in multiple transcript variants.
, interleukin 25-like
, UPF0556 protein C19orf10 homolog
, interleukin 17E