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Rat (Rattus) IL15 Kit ELISA pour Sandwich ELISA - ABIN365261
Zanchi, Lira, de Siqueira Filho, Rosa, de Oliveira Carvalho, Seelaender, Santos, Lancha: Chronic low frequency/low volume resistance training reduces pro-inflammatory cytokine protein levels and TLR4 mRNA in rat skeletal muscle. dans European journal of applied physiology 2010
Show all 2 references for ABIN365261
Mouse (Murine) IL15 Kit ELISA pour Sandwich ELISA - ABIN365238
Yin, Xu, Sun, Wei, Tian: Interleukin-15 suppresses hepatitis B virus replication via IFN-? production in a C57BL/6 mouse model. dans Liver international : official journal of the International Association for the Study of the Liver 2012
Human IL15 Kit ELISA pour Sandwich ELISA - ABIN414877
Shi, Liu, Zhang, Guo, Song, Song, Liu: miR-15b is Downregulated in Myasthenia Gravis Patients and Directly Regulates the Expression of Interleukin-15 (IL-15) in Experimental Myasthenia Gravis Mice. dans Medical science monitor : international medical journal of experimental and clinical research 2015
T cells in chimpanzees infected with human immunodeficiency virus express surface interleukin-15.
CD3 (Montrer CD3 Kits ELISA)(-) CD8 (Montrer CD8A Kits ELISA)(+) NK cells play a vital role in controlling HIV-1 infection by producing high levels of IFN-gamma (Montrer IFNG Kits ELISA), and that IL-15 elicits IFN-gamma (Montrer IFNG Kits ELISA) production in this subpopulation of NK cells in HIV-1-infected chimpanzees. [Il-15, CD8 (Montrer CD8A Kits ELISA) antigen, IFN-gamma (Montrer IFNG Kits ELISA)]
Under steady-state conditions, KLF2 (Montrer KLF2 Kits ELISA)-deficient NK cells alter their expression of homeostatic homing receptors and subsequently undergo apoptosis due to IL-15 starvation.
The induction of IgM (Montrer CD40LG Kits ELISA) and IgA, which can play pivotal roles in mucosal immunity, was promoted in the presence of IL-15. Collectively, the data implicate IL-15 as the master cytokine that induces B-1a cells to mount a mucosal immune response.
The novel mechanism of IL-15 transfer to the surface of antigen-processing DCs may explain the enhanced potency of IL-15:IL-15Ralpha-coated nanoparticles for antigen delivery.
Muscle FNDC5 (Montrer FNDC5 Kits ELISA) mRNA expression and irisin (Montrer FNDC5 Kits ELISA) release are not IL-15-dependent in mice.
Virtual memory T cells develop and mediate bystander protective immunity in an IL-15-dependent manner.
Impaired delivery of IL-15 to CD4 (Montrer CD4 Kits ELISA)+ T cells in the colon downmodulates Foxp3 (Montrer FOXP3 Kits ELISA) expression and enhances RORgammat expression. CD4 (Montrer CD4 Kits ELISA)+ T cells deprived of IL-15 trigger IBD characterized by production of pro-inflammatory cytokines and accumulation of Th1 (Montrer HAND1 Kits ELISA)/Th17 cells.
Most (86%) IL15 in serum resides in the free state, with a minor proportion (14%) residing in complex with IL15Ralpha. Results suggest that IL15 is released as a free molecule by an unknown mechanism rather than via cleavage of membrane-bound IL15/IL15Ralpha.
IL-15 may influence mononuclear phagocytes subsets in the gut (Montrer GUSB Kits ELISA) in a novel way that alters the frequency of lamina propria Th17 cells.
Downregulation of STAT3 (Montrer STAT3 Kits ELISA) phosphorylation enhances tumoricidal effect of IL-15-activated dendritic cell against doxorubicin-resistant lymphoma and leukemia via TNF-alpha (Montrer TNF Kits ELISA).
Exercise-stimulated interleukin-15 is controlled by AMPK (Montrer PRKAA1 Kits ELISA) and regulates skin metabolism and aging.
IL-15 is able to significantly regulate the inflammatory infiltration of macrophages in polymyositis patients through affecting the NF-kB pathway and MMP-9 (Montrer MMP9 Kits ELISA) expression levels.
IL-15 mRNA expression was significantly higher in patients with moderately severe viral bronchiolitis compared to controls and patients with severe disease. Serum IL15 correlated with disease severity.
These data underline the potential of "free" IL15 in the absence of Ralpha-complex as a powerful and specific immuno-modulator, which may be beneficial where selective immune-activation is desired.
Data indicate that high interleukin-16 (Montrer IL16 Kits ELISA) (IL-6 (Montrer IL6 Kits ELISA)), interferon-gamma (IFN-gamma (Montrer IFNG Kits ELISA)) and low interleukin-15 (IL-15) levels suggest active tuberculosis.
Culturing NK cells under hypoxia compared with ambient air (normoxia) and IL-15 priming synergistically augmented glycolytic gene expression without major changes in glycolytic flux and glucose consumption.
Findings suggest for co-targeting shedding-derived soluble MIC (sMIC) to enhance the therapeutic efficacy of ALT-803 or other interleukin 15 (IL-15) agonists.
Report improved antitumoral NK-cell activity in DC-based vaccine strategies through the use of IL-15/IL-15Ralpha mRNA-engineered designer DC.
results demonstrated the relative functional deficiencies of alpha-GalCer induced UCB iNKT cells, which can be ameliorated by IL-15
Myokine IL-15 regulates the crosstalk of co-cultured porcine skeletal muscle satellite cells and preadipocytes.
results demonstrate that porcine reproductive and respiratory syndrome virus (PRRSV)infection could induce IL-15 production in macrophages/dendritic cells; data further show that upregulation of IL-15 by PRRSV requires PKC (Montrer FYN Kits ELISA) and NF-kappaB (Montrer NFKB1 Kits ELISA) pathways
IFN-gamma (Montrer IFNG Kits ELISA) targets the adipocyte to induce IL-15 expression, thus indicating a possible role for the adipocyte in the regulation of T-cell function and muscle metabolism during the innate immune response
When induced by IFN-gamma (Montrer IFNG Kits ELISA) or other inflammatory mediators, IL-15 may be a significant homeorhetic factor that mobilizes and directs energy away from the adipocyte to other cells during the acute phase of the inflammatory response.
Increased function and survival of IL-15-transduced dendritic cells are mediated by up-regulation of IL-15Ralpha and Bcl-2 (Montrer BCL2 Kits ELISA).
IL 15 generates a dramatic expansion of short-lived memory CD8 (Montrer CD8A Kits ELISA) T cells and natural killer in immunocompetent macaques and has long-term effects on the balance of CD4 (Montrer CD4 Kits ELISA)(+) and CD8 (Montrer CD8A Kits ELISA)(+) T cells.
These data suggest that therapeutic use of IL-15 in the setting of antiretroviral therapy might facilitate specific restoration of the CD4 (Montrer CD4 Kits ELISA) + T cell compartment.
IL-15 secretion significantly correlates with the up-regulated expression of CD4 (Montrer CD4 Kits ELISA) on memory CD4 (Montrer CD4 Kits ELISA) T cells that is associated with increased permissiveness to simian immunodeficiency virus infection.
The protein encoded by this gene is a cytokine that regulates T and natural killer cell activation and proliferation. This cytokine and interleukine 2 share many biological activities. They are found to bind common hematopoietin receptor subunits, and may compete for the same receptor, and thus negatively regulate each other's activity. The number of CD8+ memory cells is shown to be controlled by a balance between this cytokine and IL2. This cytokine induces the activation of JAK kinases, as well as the phosphorylation and activation of transcription activators STAT3, STAT5, and STAT6. Studies of the mouse counterpart suggested that this cytokine may increase the expression of apoptosis inhibitor BCL2L1/BCL-x(L), possibly through the transcription activation activity of STAT6, and thus prevent apoptosis. Alternatively spliced transcript variants of this gene have been reported.