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IL32A encodes a member of the cytokine family. Additionally we are shipping Interleukin 32 alpha Antibodies (17) and Interleukin 32 alpha Kits (15) and many more products for this protein.
Showing 7 out of 11 products:
IL-32 (show IL32 Proteins) may be an important pro-inflammatory molecule involved in calcific aortic valve disease.
High IL32 (show IL32 Proteins) expression is associated with hepatocellular carcinoma.
Strong expression of IL-32 (show IL32 Proteins) was detected in cardiomyocytes from heart failure patients.
The increase in serum levels of IL-32 (show IL32 Proteins) in accordance with additive effect of the presence of C allele in Multiple sclerosis patients might introduce IL-32 (show IL32 Proteins) as a key player in MS pathogenesis or immunedysregulation
Collectively, these results demonstrated that IL-32alpha upregulates the atheroprotective genes Timp3 (show TIMP3 Proteins) and Reck (show RECK Proteins) by downregulating microRNA-205 through regulation of the Rprd2-Dgcr8 (show DGCR8 Proteins)/Ddx5 (show DDX5 Proteins)-Dicer1 (show DICER1 Proteins) biogenesis pathway.
high expression of both IL17A (show IL17A Proteins) and IL32 (show IL32 Proteins) leads to enhancement of T cell responses in breast tumors
High IL32 (show IL32 Proteins) expression is associated with lung metastasis in melanoma.
In Kaposi sarcoma (KS) splicing ratio of the IL-32 (show IL32 Proteins) isoforms showed IL-32gamma as the highest expressed isoform, followed by IL-32beta, in HIV-related KS cases compared with controls. Our data suggest a possible survival mechanism by the splicing of IL-32gamma to IL-32beta and also IL-6 (show IL6 Proteins), IL-8 (show IL8 Proteins), and CXCR1 (show CXCR1 Proteins) signaling pathways to reverse the proapoptotic effect of the IL-32gamma isoform, leading to tumor cell survival and th...
Three single nucleotide polymorphisms (SNPs) (rs28372698, rs12934561, rs4786370) of the IL32 (show IL32 Proteins) gene have been proposed as modifiers for different diseases. The present study found no significant differences in the genotypic frequencies between the patients and healthy controls and no relation to survival for any of the SNPs.
This study showed that the induction level of IL-32 (show IL32 Proteins) was increased in chronic rhinosinusitis with nasal polyps compared to normal nasal mucosa and that LPS (show IRF6 Proteins)-induced IL-32 (show IL32 Proteins) expression in nasal polyp-derived fibroblasts was regulated via the TLR4 (show TLR4 Proteins)/JNK (show MAPK8 Proteins)/AKT (show AKT1 Proteins)/CREB (show CREB1 Proteins) signaling pathway.
This gene encodes a member of the cytokine family. The protein contains a tyrosine sulfation site, 3 potential N-myristoylation sites, multiple putative phosphorylation sites, and an RGD cell-attachment sequence. Expression of this protein is increased after the activation of T-cells by mitogens or the activation of NK cells by IL-2. This protein induces the production of TNFalpha from macrophage cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
, interleukin-32 eta
, interleukin-32 small
, interleukin-32 theta
, natural killer cell transcript 4
, natural killer cells protein 4
, tumor necrosis factor alpha-inducing factor