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抗Mouse (Murine) TRAF6 抗体:
抗Human TRAF6 抗体:
抗Rat (Rattus) TRAF6 抗体:
Human Polyclonal TRAF6 Primary Antibody for WB - ABIN1881900
Hinz, Stilmann, Arslan, Khanna, Dittmar, Scheidereit: A cytoplasmic ATM-TRAF6-cIAP1 module links nuclear DNA damage signaling to ubiquitin-mediated NF-κB activation. in Molecular cell 2010
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Cow (Bovine) Polyclonal TRAF6 Primary Antibody for IHC (fro), IHC (p) - ABIN537432
Ichii, Otsuka, Sasaki, Namiki, Hashimoto, Kon: Altered expression of microRNA miR-146a correlates with the development of chronic renal inflammation. in Kidney international 2012
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Human Polyclonal TRAF6 Primary Antibody for ICC, ELISA - ABIN1003297
Takeda, Kaisho, Akira: Toll-like receptors. in Annual review of immunology 2003
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Human Polyclonal TRAF6 Primary Antibody for ICC, IHC (fro) - ABIN3044469
Yuan, Zhang, Yang: Ligusticum wallichii Extract Inhibited the Expression of IL-1? after AMI in Rats. in Evidence-based complementary and alternative medicine : eCAM 2014
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Human Polyclonal TRAF6 Primary Antibody for FACS, WB - ABIN4361690
Yoshida, Jono, Kai, Li: The tumor suppressor cylindromatosis (CYLD) acts as a negative regulator for toll-like receptor 2 signaling via negative cross-talk with TRAF6 AND TRAF7. in The Journal of biological chemistry 2005
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Human Polyclonal TRAF6 Primary Antibody for IF (p) - ABIN918441
Qi, Pradipta, Li, Zhao, Lu, Fu, Wei, Hsung, Tanaka, Zhou: Cinchonine induces apoptosis of HeLa and A549 cells through targeting TRAF6. in Journal of experimental & clinical cancer research : CR 2017
Human Polyclonal TRAF6 Primary Antibody for ELISA, ICC - ABIN4361694
Doyon, Servant et al.: Tumor necrosis factor receptor-associated factor-6 and ribosomal S6 kinase intracellular pathways link the angiotensin II AT1 receptor to the phosphorylation and activation of the IkappaB kinase ... in The Journal of biological chemistry 2010
Cow (Bovine) Polyclonal TRAF6 Primary Antibody for IHC, IHC (p) - ABIN4361692
Zapata, Krajewska, Krajewski, Kitada, Welsh, Monks, McCloskey, Gordon, Kipps, Gascoyne, Shabaik, Reed: TNFR-associated factor family protein expression in normal tissues and lymphoid malignancies. in Journal of immunology (Baltimore, Md. : 1950) 2000
we found that reactive oxygen species-induced autophagy acts as a negative feedback regulator of JNK (显示 MAPK8 抗体) activity by dissociating Atg9 (显示 ATG9A 抗体)/mAtg9 (显示 ATG9A 抗体) from dTRAF2/TRAF6 in Drosophila.
null mutant of DTRAF2 showed immune deficiencies in which NF-kappaB nuclear translocation and antimicrobial gene transcription against microbial infection were severely impaired
Data provide a novel association between WDFY3 (显示 WDFY3 抗体) and the RANKL (显示 TNFSF11 抗体)-induced osteoclastogenesis pathway via the modulation of TRAF6.
this study shows that TRAF6 is necessary for the nontranscriptional priming of NLRP3 (显示 NLRP3 抗体) inflammasome by TLR/IL-1R derived signals
work reveals that simulated microgravity promotes the apoptotic response through a combined modulation of the Uev1A/TICAM/TRAF (显示 TRAF1 抗体)/NF-kappaB (显示 NFKB1 抗体)-regulated apoptosis and the p53 (显示 TP53 抗体)/PCNA (显示 PCNA 抗体)- and ATM (显示 ATM 抗体)/ATR (显示 ATR 抗体)-Chk1 (显示 CHEK1 抗体)/2-controlled DNA-damage response pathways.
TRAF6 prevents the mitochondrial translocation of p53 (显示 TP53 抗体) and spontaneous apoptosis by promoting lysine63-linked ubiquitination of p53 (显示 TP53 抗体) in cytosol.
TRAF6 mediates lysine-63 ubiquitination within the SH2 (显示 MYO15 抗体) domain of STAT3 (显示 STAT3 抗体), which is an essential step for STAT3 (显示 STAT3 抗体) membrane recruitment and phosphorylation in response to S Typhimurium infection; results reveal a strategy in which S Typhimurium T3SS effectors broaden their functions through the activation of host proteins in a ubiquitination-dependent manner to manipulate host cells into becoming a Salmonella-friendly zone
this study shows that an interaction of TRAF6 with cullin-5 (显示 CUL5 抗体) promotes TRAF6 polyubiquitination and lipopolysaccharide signaling
Consistent with cellular studies, icaritin downregulated TRAF6 and NFATc1 protein expression in CD11b(+) /Gr-1(-/low) osteoclast precursors
Data (including data from studies using knockout mice) suggest that RANKL (显示 TNFSF11 抗体) enhances TNF (显示 TNF 抗体)-induced osteoclast formation from precursor spleen cells and enhances bone resorption independently of Traf6 by degrading Traf3 (显示 TRAF3 抗体), a known inhibitor of osteoclastogenesis. (RANKL (显示 TNFSF11 抗体) = osteoclast differentiation factor (显示 TNFSF11 抗体); TNF (显示 TNF 抗体) = tumor necrosis factor (显示 TNF 抗体); Traf (显示 TRAF1 抗体) = TNF (显示 TNF 抗体) receptor-associated factor)
the SH3 domain (显示 ITSN1 抗体) of NOSTRIN (显示 NOSTRIN 抗体) is involved in the NOSTRIN (显示 NOSTRIN 抗体)-TRAF6 interaction and is required for NOSTRIN (显示 NOSTRIN 抗体)-induced down-regulation of endothelial cell proteins
this study shows that TRAF6 overexpression in hematopoietic stem/progenitor cells results in impaired hematopoiesis and bone marrow failure
we have now analyzed the in vivo function of Traf6 in the innate immune response without interference of adaptive immunity
Full-length traf6 was functionally characterized.
We report two siblings with SCID (显示 PRKDC 抗体) and an atypical phenotype of osteopetrosis (OP (显示 CSF1 抗体)). A biallelic microdeletion encompassing the 5' region of TRAF6, RAG1 (显示 RAG1 抗体) and RAG2 (显示 RAG2 抗体) genes was identified. TRAF6, a tumor necrosis factor (显示 TNF 抗体) receptor-associated family member, plays an important role in T cell signaling and in RANKL (显示 TNFSF11 抗体)-dependent osteoclast differentiation and activation but its role in human OP has not been previously reported
miR (显示 MLXIP 抗体)-146a improves intestine epithelial cells survival under ischemia and I/R injury through inhibition TLR4 (显示 TLR4 抗体), TRAF6, and p-IkappaBalpha (显示 NFKBIA 抗体), subsequently leading to decreased NF-kappaB (显示 NFKB1 抗体) p65 (显示 GORASP1 抗体) nuclear translocation.
Taken together, these results define a novel role for miR (显示 MLXIP 抗体)-146a as a negative regulator of dengue virus-induced autophagy and identify TRAF6 as a key target of this microRNA in modulating the dengue virus-autophagy interaction.
These data define that YOD1 (显示 YOD1 抗体) antagonizes TRAF6/p62 (显示 GTF2H1 抗体)-dependent IL-1 (显示 IL1A 抗体) signaling to NF-kappaB (显示 NFKB1 抗体).
high expression of TRAF6 is significant for esophageal cancer progression, and TRAF6 indicates poor prognosis in esophageal cancer patients.
CRBN (显示 CRBN 抗体) negatively regulates TLR4 (显示 TLR4 抗体) signaling via attenuation of TRAF6 and TAB2 (显示 TAB2 抗体) ubiquitination.
the polymorphisms in TLR-MyD88 (显示 MYD88 抗体)-NF-kappaB (显示 NFKB1 抗体) signaling pathway confer genetic susceptibility to Type 2 diabetes mellitus and diabetic nephropathy.
The E3 ligase TRAF6 binds to DCP1a (显示 DCP1A 抗体) and indirectly regulates DCP1a (显示 DCP1A 抗体) phosphorylation, expression of decapping factors, and gene-specific mRNA decay.
Study showed that patients without a history of atrial fibrillation who develop postoperative atrial fibrillation have a higher percentage of left atrial fibrosis, increased expression of TRAF6, higher serum Ang II (显示 AGT 抗体) levels, and changes in the activities of the MAPKs/TGF-beta1 (显示 TGFB1 抗体)/TRAF6 pathway.
The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins are associated with, and mediate signal transduction from, members of the TNF receptor superfamily. This protein mediates signaling from members of the TNF receptor superfamily as well as the Toll/IL-1 family. Signals from receptors such as CD40, TNFSF11/RANCE and IL-1 have been shown to be mediated by this protein. This protein also interacts with various protein kinases including IRAK1/IRAK, SRC and PKCzeta, which provides a link between distinct signaling pathways. This protein functions as a signal transducer in the NF-kappaB pathway that activates IkappaB kinase (IKK) in response to proinflammatory cytokines. The interaction of this protein with UBE2N/UBC13, and UBE2V1/UEV1A, which are ubiquitin conjugating enzymes catalyzing the formation of polyubiquitin chains, has been found to be required for IKK activation by this protein. This protein also interacts with the transforming growth factor (TGF) beta receptor complex and is required for Smad-independent activation of the JNK and p38 kinases. This protein has an amino terminal RING domain which is followed by four zinc-finger motifs, a central coiled-coil region and a highly conserved carboxyl terminal domain, known as the TRAF-C domain. Two alternatively spliced transcript variants, encoding an identical protein, have been reported.
TNF receptor-associated factor 6-B
, E3 ubiquitin-protein ligase TRAF6
, TNF-receptor-associated factor 2
, TNF receptor-associated factor 6
, TNF receptor-associated factor 6-like
, RING finger protein 85
, interleukin-1 signal transducer
, TNF-receptor associated factor 6