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抗Human TLR6 抗体:
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Human Monoclonal TLR6 Primary Antibody for FACS, IHC (p) - ABIN252495
Hajishengallis, Tapping, Harokopakis, Nishiyama, Ratti, Schifferle, Lyle, Triantafilou, Triantafilou, Yoshimura: Differential interactions of fimbriae and lipopolysaccharide from Porphyromonas gingivalis with the Toll-like receptor 2-centred pattern recognition apparatus. in Cellular microbiology 2006
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Human Monoclonal TLR6 Primary Antibody for ELISA - ABIN4248135
Ganley-Leal, Liu, Wetzler: Toll-like receptor 2-mediated human B cell differentiation. in Clinical immunology (Orlando, Fla.) 2006
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Human Monoclonal TLR6 Primary Antibody for FACS - ABIN4360316
Wong, Cheung, Ip, Lam: Intracellular signaling mechanisms regulating toll-like receptor-mediated activation of eosinophils. in American journal of respiratory cell and molecular biology 2007
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Human Polyclonal TLR6 Primary Antibody for IHC, ELISA - ABIN1003335
Takeda, Kaisho, Akira: Toll-like receptors. in Annual review of immunology 2003
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Human Polyclonal TLR6 Primary Antibody for IF, WB - ABIN550255
Into, Kiura, Yasuda, Kataoka, Inoue, Hasebe, Takeda, Akira, Shibata: Stimulation of human Toll-like receptor (TLR) 2 and TLR6 with membrane lipoproteins of Mycoplasma fermentans induces apoptotic cell death after NF-kappa B activation. in Cellular microbiology 2004
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Human Polyclonal TLR6 Primary Antibody for ICC, ELISA - ABIN1003334
Janeway, Medzhitov: Innate immune recognition. in Annual review of immunology 2002
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Human Polyclonal TLR6 Primary Antibody for WB - ABIN550254
McGettrick, ONeill: The expanding family of MyD88-like adaptors in Toll-like receptor signal transduction. in Molecular immunology 2004
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Human Polyclonal TLR6 Primary Antibody for IHC, IHC (fro) - ABIN4890204
Morgan, Koelink, Zheng, den Brok, van de Kant, Verspaget, Folkerts, Adema, Kraneveld: Toll-like receptor 6 stimulation promotes T-helper 1 and 17 responses in gastrointestinal-associated lymphoid tissue and modulates murine experimental colitis. in Mucosal immunology 2014
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Human Monoclonal TLR6 Primary Antibody for FACS, IF - ABIN2192072
Nakao, Funami, Kikkawa, Taniguchi, Nishiguchi, Fukumori, Seya, Matsumoto: Surface-expressed TLR6 participates in the recognition of diacylated lipopeptide and peptidoglycan in human cells. in Journal of immunology (Baltimore, Md. : 1950) 2005
Human Polyclonal TLR6 Primary Antibody for FACS, IF (p) - ABIN749573
Shmuel-Galia, Aychek, Fink, Porat, Zarmi, Bernshtein, Brenner, Jung, Shai: Neutralization of pro-inflammatory monocytes by targeting TLR2 dimerization ameliorates colitis. in The EMBO journal 2016
TLR6 single nucleotide polymorphisms rs3796508 (Val327Met) and rs5743810 (Ser249Pro) and breast cancer susceptibility in Saudi Arabian women were evaluated. The findings suggest a strong association between rs5743810 and protection against Breast Cancer risk in Saudi Arabian women. Importantly, the rs5743810 Pro allele could be a potential Breast Cancer diagnostic biomarker in this ethnic population.
Live Faecalibacterium prausnitzii, an abundant obligate anaerobe of the colonic microbiota, induced higher TLR2 and TLR2/6 activation than the dead bacterium.
mean proportions of European ancestry differed significantly between the genotypes of the TLR1 (I602S) gene in a population of the Atlantic Forest, Sao Paulo, Brazil
Identification of TLR2/TLR6 signalling lactic acid bacteria for supporting immune regulation.
recombinant NS1, expressed and purified from eukaryotic cells, induces cytokine production via TLR4 but not TLR2/6.
TLR6 role in Kawasaki disease susceptibility in African American family
The mRNA levels of Toll-like receptors TLR2, 6, and 9 were significantly elevated in the Kawasaki disease (KD) patient group versus the healthy controls.
Significant correlations with atherosclerosis susceptibility were found for the toll like receptor 1 (TLR1) rs5743551 polymorphism and toll like receptor 6 (TLR6) rs5743810 polymorphism.
Study concludes that genetic variation in the TLR10-TLR1-TLR6 gene cluster mediates responsiveness to organic dust, but indicates different signaling pathways for IL-6 and TNF-alpha. These studies provide new insight into the role of the TLR10-TLR1-TLR6 gene cluster and the innate immune response to organic dust.
Studied the relationship between polymorphisms in MBL, TLR1, TLR2 and TLR6 encoding genes and stimulated IFN-gamma and IL-12 ex vivo production in BCG osteitis survivors. Found that variant genotypes of the MBL2 gene (if homozygous) and variant genotypes of the TLR2 gene (only heterozygotes present) are associated with low IFN-gamma production.
efficient method for preparation of the extracellular domain of human Toll-like receptor 6 (TLR6ED) in Escherichia coli using the bubbling cultivation method. Our preparation method improved the level of expression of TLR6ED into a soluble fraction as compared with typical cultivation using a rotary shaker. Circular dichroism (CD) experiments confirmed the structural formation of TLR6ED with secondary structure contents
Toll-like receptor 6 (TLR6) is significantly overexpressed in the hepatocytes of non-alcoholic fatty liver disease (NAFLD patients compared to their normal counterparts.
study demonstrates a significant association between TLR4 rs192791 and TLR6 rs1039559 SNPs and posttransplantation diabetes mellitus in renal transplantation recipients
genetic polymorphism is associated with malaria disease progression in Indian patients
Study showed that MyD88 Toll/interleukin-1 receptor (TIR) domain interacted with TLR5TIR but not with TLR6TIR. The solubility of both TLR5TIR and TLR6TIR were influenced by its binding partner MyD88TIR.
Study annotated variants at 4p14 as expression quantitative trait loci (eQTL) associated with TLR6/10 and FAM114A1; findings suggest that 4p14 polymorphisms are linked to host immune response to H. pylori infection but not to its acquisition.
OSA patients had increased TLR2/6 co-expressions on blood immune cells, which were related to their immune cell counts and could be reversed with CPAP treatment. In vitro IHR could induce TLR2/6 co-upregulation.
TLR7 rs179008 showed some associations with post-bronchiolitis lung function deficiency, and polymorphisms of TLR4 rs4986790, and TLR6 rs5743810 in particular, with airway reactivity.
Dengue virus NS1 protein is the viral protein responsible for the activation of TLR2 and TLR6 during Dengue virus infection
study found TLR6 gene rs3775073 polymorphism may be associated with 2-fold decrease of infective endocarditis risk
Light Guided In-vivo Activation of Innate Immune Cells with Photocaged TLR 2/6 Agonist.
findings show that TLR6 and mannose receptor participate as macrophage receptors for Mycobacterium lepraemurium
the cooperative role of TLR9 with TLR2 or TLR6 receptors in sensing Brucella, was determined.
Data suggest that the transmembrane domains of Tlr4 and Tlr6 have essential roles in Tlr4/Tlr6/Cd36 receptor multimerization and activation; disruption of receptor multimerization (here, using a recombinant peptide fragment from Tlr4 transmembrane domain) reduces secretion of proinflammatory mediators from microglia and ultimately rescues neurons from death.
TLR6 knockout alleviates generation of myocardial fibrosis by suppressing collagen deposition.
Hepatic expression of Tlr6, but not that of Tlr8 is epigenetically controlled, and that the dysregulations of Tlr6 and Tlr8 critically contribute to Testosterone (T)-induced persistent susceptibility to P. chabaudi malaria.
lipopeptides elicit TLR1/2 and TLR2/6 signaling in the endolysosomes, but not on the cell surface.
Transmembrane oligomeric form of Vibrio cholerae cytolysin (VCC) triggers TLR2/TLR6-dependent proinflammatory responses in monocytes and macrophages.
The inhibition of TLR receptors 2 and 6 in the presence of their specific ligands restored the ability of the spheroids to bind to the endometrial cells.
long-term exposure to nicotine up-regulated the expression of TLR4 and -6 via a JNK-related pathway, causing an exaggeration of the LPS-induced local airway inflammation and increased airway hyperreactivity
The results demonstrate that inflammatory responses caused by ZNPs-activated macrophages strongly depend on TLR6-mediated MAPK signalling.
aortic angiogenesis is preceded by an immune reaction with overexpression of Toll-like receptors (TLRs) and TLR-inducible genes.
TLR6 on bone marrow dendritic cells can sense Mycobacterium avium and this receptor is required for full resistance to M. avium infections.
The toll-like receptor 2/6 agonist MALP-2 promotes reendothelialization and inhibits neointima formation after experimental vascular injury via enhanced proliferation and migration of endothelial cells.
In this study, we report that transmembrane domain (TMD)-derived peptides from TLR2 and TLR6 specifically inhibit TLR2 activation
the results presented here indicate that TLR6 is required to trigger innate immune responses against B. abortus in vivo and is required for the full activation of dendritic cells to induce robust proinflammatory cytokine production.
Innate immune detection of Aspergillus fumigatus is mediated by TLR4 and TLR2 together with TLR1 or TLR6 in mice.
TLR6 activation is critical for IL-23 production and Th17 responses, which both regulate the allergic inflammatory response in chronic fungal-induced asthma.
In total, 20, 27, and 26 SNPs were detected in TLR1, TLR2, and TLR6, respectively; SNPs detected in TLR6 may represent species-specific function on the protein level in the wild boars and domestic pigs.
both TLR2 and TLR6 are important in the recognition of M. hyopneumoniae in porcine alveolar macrophages
phylogenetic analysis of the cytoplasmic regions of TLR genes suggested that the signal transduction pathway of TLR10 was different from those of TLR1 and TLR6
Variants in the TLR6 gene are associated with susceptibility to bovine TB.
TLR2, TLR1, and TLR6 haev roles in innate immunity and initiate inflammatory responses to bacterial lipopeptides by epithelial and stromal cells of bovine endometrium
The expression analysis showed similar expression profiles for TLR1 and TLR6, which indicate a co-regulation of these two genes, TLR10 had a different expression profile, pointing toward a stronger functional diversification compared to TLR1 and TLR6.
Analysis of sequence variability and protein domain architectures for bovine peptidoglycan recognition protein 1 and Toll-like receptors 2 and 6.
The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This receptor functionally interacts with toll-like receptor 2 to mediate cellular response to bacterial lipoproteins. A Ser249Pro polymorphism in the extracellular domain of the encoded protein may be associated with an increased of asthma is some populations.
toll-like receptor 1 type 1
, toll-like receptor 16
, toll-like receptor1