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anti-Mouse (Murine) IL12A Antibodies:
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Human Monoclonal IL12A Primary Antibody for CyTOF, FACS - ABIN4899730
Liu, Bi, Xue, Zhang, Yang, Chen, Lu, Zhang, Liu, Wang, Wang, Chu, Yang: Dendritic cell SIRT1-HIF1α axis programs the differentiation of CD4+ T cells through IL-12 and TGF-β1. in Proceedings of the National Academy of Sciences of the United States of America 2015
Show all 10 Pubmed References
Human Monoclonal IL12A Primary Antibody for CyTOF, FACS - ABIN4899729
Kochetkova, Thornburg, Callis, Holderness, Maddaloni, Pascual: Oral Escherichia coli colonization factor antigen I fimbriae ameliorate arthritis via IL-35, not IL-27. in Journal of immunology (Baltimore, Md. : 1950) 2014
Show all 10 Pubmed References
Human Monoclonal IL12A Primary Antibody for FACS - ABIN4896565
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 IL12A Primary Antibody for FACS - ABIN4896566
Richter, Thieme, Bandoła, Laugsch, Anastassiadis, Brenner: Generation of inducible immortalized dendritic cells with proper immune function in vitro and in vivo. in PLoS ONE 2013
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Human Monoclonal IL12A Primary Antibody for FACS - ABIN4896563
van Herwijnen, Wieten, van der Zee, van Kooten, Wagenaar-Hilbers, Hoek, den Braber, Anderton, Singh, Meiring, van Els, van Eden, Broere: Regulatory T cells that recognize a ubiquitous stress-inducible self-antigen are long-lived suppressors of autoimmune arthritis. in Proceedings of the National Academy of Sciences of the United States of America 2012
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findings show that IL-12 and other proinflammatory cytokines transduce signals through the TCR signalosome in a manner that requires Fyn activity and self-peptide-MHC (self-pMHC) interactions.
this study shows that a systemic IL-12 primes intestinal cells that became more prone to develop inflammatory responses, which is long-lasting because intestinal cells maintain their inflammatory potential and their ability to aggravate colitis
These results suggest a correlation between CRMP2 (show DPYSL2 Antibodies) phosphorylation and AD pathophysiology, and indicate the effectiveness of pioglitazone treatment at the pre-Abeta (show APP Antibodies) accumulation stage in AD model mice.
Data show that interleukin-35 (Epstein-Barr virus-induced gene 3 (EBI3) and the interleukin-12 Subunit p35 (p35) subunit) expressing plasmid downregulates the expression of pro-inflammatory cytokines and upregulates the expression of anti-inflammatory cytokines.
Data suggest that interleukin-35 (Epstein-Barr virus-induced gene 3 (EBI3) and the interleukin-12 Subunit p35 (p35) subunit) contributes to the increased susceptibility to secondary pneumococcal pneumonia.
Deficiency of IL-12p35 limited AMI (show CFD Antibodies)-induced cardiac injury by promoting pro-angiogenesis and anti-inflammatory functions of monocytes
IL-12 immunomodulation delays the onset of lethal peritoneal disease of ovarian cancer.
There is a common program of effector T cell differentiation that is regulated by IL-2 and IL-12 signaling and the combined activities of the transcriptional regulators Blimp-1 and T-bet.
Irradiation-induced IL-6 (show IL6 Antibodies) can decrease IL-12 production through the inhibition of C-Rel (show NFkBP65 Antibodies) phosphorylation by the IL-6 (show IL6 Antibodies)/STAT3 (show STAT3 Antibodies) signaling pathway.
The IL-12 response by dendritic cells against S. aureus is highly growth phase dependent.
Epstein Barr Virus miRNAs collectively and specifically suppress release of proinflammatory cytokines such as IL-12, repress differentiation of naive CD4 (show CD4 Antibodies)(+) T cells to Th1 (show TH1L Antibodies) cells.
HLA-B51 is a primary association marker in predisposition to Behcet disease, with IL-23R and IL12A being the additional strongest loci.
assembly-induced folding is key in IL-12 family biogenesis and secretion; the identification of essential disulfide bonds that underlie this process lays the basis for a simplified yet functional IL-12 cytokine
The plasma levels of interleukin-35 were significantly higher in the hepatocellular carcinoma patients than the controls.
Importantly, treatment of NK cells from HIV-infected patients with IL-12 reversed the multiple defects in binding, granule polarization, perforin (show PRF1 Antibodies) content, and perforin (show PRF1 Antibodies) release and restored anticryptococcal activity.
Our results from a large-scale population-based study suggest that there are differences in levels of adiponectin (show ADIPOQ Antibodies), IL-10 (show IL10 Antibodies) and IL-12 between neonates that later develop T1D compared to their healthy controls
this study shows that that IL-12 and IL-4 (show IL4 Antibodies) govern group 2 innate lymphoid cells functional identity and that their imbalance results in the perpetuation of type 1 or type 2 inflammation
The results of this case-control study suggest that IL-12A, IL-12B (show IL12B Antibodies), IL12RB1 (show IL12RB1 Antibodies), IL12RB2 (show IL12RB2 Antibodies) and IL23R (show IL23R Antibodies) make no genetic contribution to the susceptibility of Takayasu arteritis in Chinese populations
suberoylanilide hydroxamic acid significantly inhibited IL-12p40 and IL-23p19 mRNA synthesis and did not change IL-12p35 mRNA transcription.
this study shows that IL-12A gene polymorphism contributes to the risk of hepatocellular carcinoma on top of chronic hepatitis C virus infection in Egyptian patients
The results showed that the expression of TNF-alpha (show TNF Antibodies), iNOS (show NOS2 Antibodies), and IL-6 (show IL6 Antibodies) in alveolar macrophages was up-regulated by stimulation with the recombinant Mce4A protein of M. bovis; in contrast, expression of IL-12 was unaffected.[IL-6 (show IL6 Antibodies), IL-12]
This gene encodes a subunit of a cytokine that acts on T and natural killer cells, and has a broad array of biological activities. The cytokine is a disulfide-linked heterodimer composed of the 35-kD subunit encoded by this gene, and a 40-kD subunit that is a member of the cytokine receptor family. This cytokine is required for the T-cell-independent induction of interferon (IFN)-gamma, and is important for the differentiation of both Th1 and Th2 cells. The responses of lymphocytes to this cytokine are mediated by the activator of transcription protein STAT4. Nitric oxide synthase 2A (NOS2A/NOS2) is found to be required for the signaling process of this cytokine in innate immunity.
, IL-12 subunit p35
, cytotoxic lymphocyte maturation factor 35 kDa subunit
, interleukin 12a p35 subunit
, interleukin-12 subunit alpha
, interleukin 12 p35 subunit
, IL-12, subunit p35
, IL35 subunit
, NF cell stimulatory factor chain 1
, NK cell stimulatory factor chain 1
, cytotoxic lymphocyte maturation factor 1, p35
, interleukin 12, p35
, interleukin-12 alpha chain
, natural killer cell stimulatory factor 1, 35 kD subunit
, interleukin 12 35kDa subunit
, interleukin 12 polypeptide 35
, natural killer cell stimulatory factor 1, cytotoxic lymphocyte maturation factor 1, p35
, interleukin 12B
, interleukin-12 p35 subunit
, IL-12 p35
, interleukin 12
, Cytotoxic lymphocyte maturation factor 35 kDa subunit
, interleukin 12 35kD subunit
, IL-12p35 subunit