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anti-Human IL-10 Antibodies:
anti-Mouse (Murine) IL-10 Antibodies:
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Human Monoclonal IL-10 Primary Antibody for - ABIN1383949
Schandené, Alonso-Vega, Willems, Gérard, Delvaux, Velu, Devos, de Boer, Goldman: B7/CD28-dependent IL-5 production by human resting T cells is inhibited by IL-10. in Journal of immunology (Baltimore, Md. : 1950) 1994
Show all 11 Pubmed References
Human Polyclonal IL-10 Primary Antibody for WB - ABIN3042618
Presti, DOrazio, Labra, La Ferla, Mezzasalma, Bizzaro, Giardina, Michelotti, Tursi, Vassallo, Di Gennaro: Evaluation of the probiotic properties of new Lactobacillus and Bifidobacterium strains and their in vitro effect. in Applied microbiology and biotechnology 2015
Show all 10 Pubmed References
Cow (Bovine) Polyclonal IL-10 Primary Antibody for IHC, ELISA - ABIN1582204
Shi, Diez-Freire, Jun, Qi, Katovich, Li, Sriramula, Francis, Sumners, Raizada: Brain microglial cytokines in neurogenic hypertension. in Hypertension 2010
Show all 7 Pubmed References
Rat (Rattus) Polyclonal IL-10 Primary Antibody for IHC (p), ELISA - ABIN3042802
Gao, Zhao, Liu, Yuan, Wu, Xia: Myocardial ischemic post-conditioning protects the lung against myocardial ischemia/reperfusion-induced damage by activating GSK-3β. in Acta cirurgica brasileira 2017
Show all 6 Pubmed References
Human Monoclonal IL-10 Primary Antibody for ELISA, IHC - ABIN4324436
Sahoo, Dey, Maiti: pSiM24 is a novel versatile gene expression vector for transient assays as well as stable expression of foreign genes in plants. in PLoS ONE 2014
Show all 6 Pubmed References
Human Monoclonal IL-10 Primary Antibody for ELISA (Capture), FACS - ABIN967464
Just, Abrams, Louie, Urbano, Wara, Nicholas, Stein, King: Influence of host genotype on progression to acquired immunodeficiency syndrome among children infected with human immunodeficiency virus type 1. in The Journal of pediatrics 1995
Show all 8 Pubmed References
Mouse (Murine) Polyclonal IL-10 Primary Antibody for ELISA, WB - ABIN3042803
Jin, Yang, Song, Zhang, Li: Protective roles of quercetin in acute myocardial ischemia and reperfusion injury in rats. in Molecular biology reports 2012
Show all 5 Pubmed References
Human Monoclonal IL-10 Primary Antibody for ICC - ABIN2689715
Abrams, Roncarolo, Yssel, Andersson, Gleich, Silver: Strategies of anti-cytokine monoclonal antibody development: immunoassay of IL-10 and IL-5 in clinical samples. in Immunological reviews 1992
Show all 5 Pubmed References
Human Polyclonal IL-10 Primary Antibody for ELISA, IF (p) - ABIN672051
Kou, Hu, Yao, Wang, Shen, Kang, Hong: Transforming growth factor-?1 promotes Treg commitment in nasal polyposis after intranasal steroid treatment. in Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2013
Show all 5 Pubmed References
Human Monoclonal IL-10 Primary Antibody for ELISA, WB - ABIN2689726
Burdin, Péronne, Banchereau, Rousset: Epstein-Barr virus transformation induces B lymphocytes to produce human interleukin 10. in The Journal of experimental medicine 1993
Show all 4 Pubmed References
IL-27 (show IL27 Antibodies) is a pivotal regulator in endometriotic immune tolerance by triggering Th17 cells to produce IL-10.
Macrophage-derived IL-10 has a role in mediating mucosal repair by epithelial WISP-1 (show WISP1 Antibodies) signaling
The results obtained suggest that both studied IL28B (show IL28B Antibodies) gene SNPs (single nucleotide polymorphisms), as well as the IL10 gene rs1800872 SNP are associated with predisposition to tick-borne encephalitis in Russian population.
When combined with previous studies, however, a significant relationship between IL-10- 1082A/G and ischemic stroke risk was found (G vs. A: OR= 0.73, 95% CI = 0.60-0.88, p < 0.01; GG vs. AA: OR= 0.61, 95% CI = 0.49-0.76, p < 0.01; GG+AG vs. AA: OR= 0.70, 95% CI = 0.54-0.91, p < 0.01; GG vs. AG+AA: OR= 0.68, 95% CI = 0.52-0.89, p < 0.01), as well as in subgroup analyses.
The increase in the frequency of Treg cells and IL-10 levels was associated with a decrease in IL-17 (show IL17A Antibodies) in patients receiving tuberculosis treatment.
Conducted a meta-analysis to study the effects of IL10 gene polymorphisms (-1082G/A, -819C/T, -592C/A) and their haplotypes on sustained virological response (SVR) in chronic hepatitis C(CHC (show CLTC Antibodies)) patients receiving pegylated interferon alpha (show IFNA Antibodies) (PEG (show PAEP Antibodies)-IFN-a (show IFNA6 Antibodies)) plus ribavirin. Results found IL10-1082GG genotype and -1082G allele associated with dec'd SVR rate in CHC (show CLTC Antibodies) patients; IL10-819T allele more likely to get SVR in Caucasians.
Study assessed the influence of TNF-alpha (show TNF Antibodies) and IL-10 single nucleotide polymorphisms on the progression of HCV-induced chronic hepatitis to cirrhosis in HIV-coinfected patients; -238 TNF-alpha (show TNF Antibodies) (rs361525) and IL-10 (rs1800872) assessed; in this cohort of Caucasian patients, TNF-alpha (show TNF Antibodies) -238 polymorphism was involved in the risk of liver cirrhosis.
suggest epigenetic control of IL-10 production
The inhibitory properties of bronchial endothelial cellss are dysregulated in stable lung transplant recipients via TGF-beta (show TGFB1 Antibodies), IL-10 and HLA-G (show HLAG Antibodies) signaling pathway.
associations between the genetic variants and the LPS (show IRF6 Antibodies)-induced IL-6 (show IL6 Antibodies), IL-8 (show IL8 Antibodies), IL-10, IL-1ra (show IL1RN Antibodies) and TNF-alpha (show TNF Antibodies) cytokine levels were not significant in the meta-analysis. This present study does not support a strong genetic effect of LPS (show IRF6 Antibodies)-stimulated cytokine production; however, the potential for type II errors should be considered
Antigen targeting to DEC-205 (show LY75 Antibodies) on dendritic cells leads to an IL-10-dependent downregulation of CXCR3 (show CXCR3 Antibodies) expression on differentiated antigen-specific Th1 (show HAND1 Antibodies) cells in vivo. This downregulation interferes with the migration of Th1 (show HAND1 Antibodies) cells into the gut (show GUSB Antibodies) and protects mice against severe acute and relapsing intestinal inflammation.
The investigation of the IL-10R complex revealed that both the extracellular and intracellular domains of IL-10R2 (show IL10RB Antibodies) influence the conformation of IL-10R1 (show IL10RA Antibodies) and that both domains were required for transducing IL-10 signals.
identification of the Mediator-associated kinase CDK8 (show CDK8 Antibodies), and its paralog CDK19 (show CDK19 Antibodies), as negative regulators of IL-10 production during innate immune activation
ablation of IL-10 signaling in Th2 cells led to enhanced Th2 cell survival and exacerbated pulmonary inflammation in a murine model of house dust mite allergy
Differential Production of Type I IFN Determines the Reciprocal Levels of IL-10 and Proinflammatory Cytokines Produced by C57BL/6 and BALB/c Macrophages
Virulence-dependent induction of interleukin-10-producing-tolerogenic dendritic cells by Mycobacterium tuberculosis impedes optimal T helper type 1 proliferation
The defective IL-10 production by PGRN (show GRN Antibodies)-deficient cells is primarily due to reduced C/EBPalpha (show CEBPA Antibodies) protein stability via the E3 ubiquitin-conjugating enzyme (show Ube2t Antibodies) E6AP (show ube3a Antibodies) and proteasome-mediated degradation.
IL-6 (show IL6 Antibodies) directly increases IL-10 production and participates in the counter-inflammatory response after acute kidney injury.
This study reveals the striking ability of a prototypical innate immune receptor to trigger a potent and suppressive IL-10 response in effector/memory T cells, supporting the notion that TLR2 (show TLR2 Antibodies) is a co-regulatory receptor on T cells.
data reveal that, despite the multiple immune sources of IL-10 during M. tuberculosis infection, activated effector T cells are the major source accounting for IL-10-induced TB susceptibility.
This study seems to indicate that PGE2 in cattle does not produce an anti-inflammatory effect by increasing the synthesis of IL-10.
IL-10 mRNA expression increased on day 8 in the mononuclear leukocytes of pregnant cows. In a cell culture experiment, interferon-tau stimulated stimulated IL-10 mRNA expression in mononuclear leukocytes.
Bovine IL-10 potently inhibits the activation of human myeloid cells in response to toll (show TLR4 Antibodies) like receptor activation.
Monocytes obtained from cows with subclinical infection with MAP had upregulated expression of IL-10 and SOCS-3 (show SOCS3 Antibodies), which may have attenuated the capacity of mononuclear phagocytes to initiate inflammatory and adaptive immune responses.
The ability of an EHV-1 isolate to down-regulate IL-10 production might contribute to increased local inflammation and a higher risk for neurological manifestation of the disease after infection with Ab4.
The data suggested in foals there is an impaired Th2 response, the immune response is Th1 (show TH1L Antibodies) biased, interferon-gamma (show IFNG Antibodies) production is qualitatively similar to adult horses, and regulatory IL-10 production by T cells is mature.
serum IL-6 (show IL6 Antibodies):IL-10 ratio is likely to provide a valuable prognosticator for neonatal septicemia
The contribution of bronchial epithelium to airway inflammation, with focus on mRNA and protein expression of IL-6 (show IL6 Antibodies), IL-10 and TNF-alpha (show TNF Antibodies), in horses with recurrent airway obstruction during exacerbation and in remission is reported.
The complete open reading frame consists of 537 base pairs which encodes a protein of 179 amino acids. This cDNA sequence exhibited 87% homology with human IL-10.
ICAM1 (show ICAM1 Antibodies) and IL10 were upregulated in ventilator-induced lung injury. Nuclear transcription factor AP-1 (show JUN Antibodies) may be responsible for this upregulation.
The PRRSV vaccination induced higher levels of IL-10 expression in the first week and this may be why the CSFV vaccination is immunosuppressed.
These data indicate that the type 2 porcine reproductive and respiratory syndrome virus N protein plays an important role in IL-10 induction and the N-N non-covalent domain is associated with this activity.
The effects of semen, spermatozoa in extender, or extender alone on the expression of TGF-beta1 (show TGFB1 Antibodies), IL-10, and IL-6 (show IL6 Antibodies) in ovarian follicles are reported.
Prostaglandin E2 potentiates mesenchymal stem cell-induced IL-10+IFN-gamma (show IFNG Antibodies)+CD4 (show CD4 Antibodies)+ regulatory T cells to control transplant arteriosclerosis.
Porcine reproductive and respiratory syndrome virus strain CH-1a could significantly up-regulate IL-10 production through p38 MAPK (show MAPK14 Antibodies) activation.
Boar seminal plasma contained TGF- beta1 (show TGFB1 Antibodies) and IL-10 but with high individual variation.
Changes in interleukin-10 mRNA expression are predictive for 9-day survival of pigs in an emergency preservation and resuscitation model.
These results suggest that TNF-alpha (show TNF Antibodies) and IL-10, but not IL-6 (show IL6 Antibodies), are involved in the late reparatory phases of the experimental disk lesion.
The present study shows that elevated levels of serum CRP (show CRP Antibodies) and IL-10 were associated with porcine circovirus type 2-infected piglets that subsequently developed severe PMWS.(postweaning multisystemic wasting syndrome)
Subclinically porcine circovirus type 2 (PCV2)-infected pigs developed a transient PCV2-specific IL-10 response during the viremic phase of infection which coincided with the inversion of the IgM/IgG ratio.
IL-10 produced during the immune response to malaria in this model contributes to suppression of mucosal inflammatory responses to invasive NTS (show NTS Antibodies), which may contribute to differences in the clinical presentation of NTS (show NTS Antibodies) infection in the setting of malaria.
Findings demonstrate that internalization of IL-10R with the resultant impact on IL-10 signaling and dysregulation of the IL-10-mediated anti-inflammatory responses might play a crucial role in epithelial cell damage and subsequent simian immunodeficiency virus pathogenesis.
IL-10 plays a crucial role in maintaining mucosal homeostasis by regulating mucosal IFNgamma and TNFalpha (show TNF Antibodies) cytokine production.
The protein encoded by this gene is a cytokine produced primarily by monocytes and to a lesser extent by lymphocytes. This cytokine has pleiotropic effects in immunoregulation and inflammation. It down-regulates the expression of Th1 cytokines, MHC class II Ags, and costimulatory molecules on macrophages. It also enhances B cell survival, proliferation, and antibody production. This cytokine can block NF-kappa B activity, and is involved in the regulation of the JAK-STAT signaling pathway. Knockout studies in mice suggested the function of this cytokine as an essential immunoregulator in the intestinal tract. Mutations in this gene are associated with an increased susceptibility to HIV-1 infection and rheumatoid arthritis.
T-cell growth inhibitory factor
, cytokine synthesis inhibitory factor
, uncharacterized protein LOC100715618
, Cytokine synthesis inhibitory factor