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The protein encoded by IL25 is a cytokine that shares sequence similarity with interleukin 17. Additionally we are shipping IL25 Kits (64) and IL25 Proteins (64) and many more products for this protein.
Showing 10 out of 256 products:
Human Monoclonal IL25 Primary Antibody for CyTOF, FACS - ABIN4900222
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
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Human Monoclonal IL25 Primary Antibody for CyTOF, FACS - ABIN4900221
Kan, de Jager, de Wit, Heijnen, van Zuiden, Ferrier, van Rijen, Gosselaar, Hessel, van Nieuwenhuizen, de Graan: Protein expression profiling of inflammatory mediators in human temporal lobe epilepsy reveals co-activation of multiple chemokines and cytokines. in Journal of neuroinflammation 2012
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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
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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
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Human Monoclonal IL25 Primary Antibody for FACS, WB - ABIN1043787
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
Human Polyclonal IL25 Primary Antibody for IF (p), IHC (p) - ABIN748013
Al-Samadi, Moossavi, Salem, Sotoudeh, Tuovinen, Konttinen, Salo, Bishehsari: Distinctive expression pattern of interleukin-17 cytokine family members in colorectal cancer. in Tumour biology 2015
study concludes that IL-33 (show IL33 Antibodies) and TSLP (show TSLP Antibodies) are required for epithelial cell IL-25 expression, mucous metaplasia, and ILC2 expansion following early-life rhinovirus infection
IL-17E (IL-25) and IL-17RB promote respiratory syncytial virus-induced pulmonary disease
data suggested that deletion of Shp2 (show PTPN11 Antibodies) impaired IL-25 production in bronchial epithelial cells in vitro, but might yet have minor influence on OVA-induced allergic reaction in vivo
study showed that IL-25 promoted the accumulation of ICOS (show ICOS Antibodies) and T1/ST2 on nuocytes, further induced the pro-inflammatory Th2 cells, and promoted Th2 cytokine responses in OVA-induced airway inflammation
Inhibition of IL-25 resulted in decreased type 2 T cells and macrophages in the primary tumor microenvironments, both reported to enhance breast tumor invasion and subsequent metastasis to the lung.
this study shows that activation of primed TH2 cells occurs independently of group 2 innate lymphoid cells or their cytokines but that the effector function of both cell types was dependent on combinatorial exposure to IL-33 (show IL33 Antibodies), IL-25 and TSLP (show TSLP Antibodies)
These data demonstrate that IL-25 is critical for host protective immunity against H. polygyrus bakeri infection, highlighting its potential application as a therapeutic agent against parasitic nematode infection worldwide.
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
Nasal Il-25 is overexpressed in patients with chronic rhinosinusitis with nasal polyps and airway hypersensitiveness.
IL-4 (show IL4 Antibodies) signaling up-regulates the IL-25 axis in human monocytic cells, and IL-25 may provide autocrine signals in monocytes and macrophages to sustain IL-17Rb expression and predispose to alternative activation.
IL-25-induced activation of nasal fibroblast and its association with the remodeling of chronic rhinosinusitis with nasal polyposis
The authors concluded that IL-25 provides protection from amebiasis, which is dependent upon intestinal eosinophils and suppression of TNF-alpha (show TNF Antibodies).
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.
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