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anti-Mouse (Murine) RNASEL Anticorps:
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Hamster Monoclonal RNASEL Primary Antibody pour IHC (p), IHC - ABIN151816
Al-Ahmadi, Al-Ghamdi, Al-Haj, Al-Saif, Khabar: Alternative polyadenylation variants of the RNA binding protein, HuR: abundance, role of AU-rich elements and auto-Regulation. dans Nucleic acids research 2009
Show all 9 Pubmed References
Monoclonal RNASEL Primary Antibody pour ELISA, WB - ABIN534101
Wang, Zhou, Vasavada, Dong, Nie, Church, Williams, Banerjee, Silverman: Elevated levels of 2',5'-linked oligoadenylate-dependent ribonuclease L occur as an early event in colorectal tumorigenesis. dans Clinical cancer research : an official journal of the American Association for Cancer Research 1999
Show all 4 Pubmed References
Pref-1 (Montrer DLK1 Anticorps) mRNA is a novel substrate of RNase-L.
RNAse L stimulates fibroblast migration.
Thus, activation of RNase L does not require mouse hepatitis virus virus-induced interferon (Montrer IFNA Anticorps) but rather correlates with adequate levels of basal Oas (Montrer SMOC1 Anticorps) gene expression, maintained by basal interferon (Montrer IFNA Anticorps) signaling.
Thus, RNA cleavage events catalyzed by RNase L are required for optimal inflammasome activation during viral infections.
cellular functions of RNase L through protein-protein interactions in the spleen for immune response in mammals
Data indicate that deficiency of 2-5A-dependent RNase L (RNase L) in resulted in a significant delay of diabetes onset.
RNase L contributes to innate immunity through regulating macrophage functions.
By targeting the effector enzyme of this antiviral pathway, L* potently inhibits RNase L, underscoring the importance of this enzyme in innate immunity against Theiler's virus.
RNase-L deficiency exacerbates experimental colitis and colitis-associated cancer.
These studies highlight novel roles of RNase L in cigarette smoke plus virus induced inflammation, tissue remodeling, apoptosis, and cytokine elaboration
These results demonstrate that ablation of RNase L activity promotes survival of ADAR1 (Montrer ADAR Anticorps) deficient cells even in the presence of MDA5 (Montrer IFIH1 Anticorps) and MAVS (Montrer MAVS Anticorps), suggesting that the RNase L system is the primary sensor pathway for endogenous dsRNA that leads to cell death.
Mutations in the genes glucokinase regulatory protein (GCKR (Montrer GCKR Anticorps)), RNase L (RNASEL), leukocyte immunoglobulin-like receptor 3 (Montrer LILRB3 Anticorps) (LILRA3 (Montrer LILRA3 Anticorps)), and dynein axonemal heavy chain 10 (DNAH10 (Montrer DNAH10 Anticorps)) segregated with elevated HDLc levels in families, while no mutations associated with low HDLc.
findings suggest that beside the RLR (Montrer DHX58 Anticorps) pathway, RNase L cleavage products can also activate the NLRP3 (Montrer NLRP3 Anticorps)-inflammasome pathway, which requires DHX33 (Montrer DHX33 Anticorps) (DExD/H-box helicase) and the mitochondrial adaptor protein MAVS (Montrer MAVS Anticorps).
This study provides the evidence that germline variations in RNASEL are associated with fatal PCa (Montrer FLVCR1 Anticorps) in men (Gleason score >7 for rs486907 and RNASEL underexpressed [P = 0.007] in patients with PCa (Montrer FLVCR1 Anticorps)).
By sequencing abundant RNA fragments generated by RNase L in cell lines, we identify site-specific cleavage of two groups of noncoding RNAs: Y-RNAs, whose function is poorly understood, and cytosolic tRNAs, which are essential for translation.
RNASEL rs3738579 genotype was significantly related to severe necroinflammatory activity (NIA) grade of chronic hepatitis C patients.
Serum RNase-L levels were inversely associated with metabolic syndrome and age.
We show that mutations in RNase L found in HPC patients may promote prostate cancer by increasing expression of AR-responsive genes and cell motility and identify novel roles of RNase L as a prostate cancer susceptibility gene.
Suggest that naturally occurring mutations in the RNase L gene might promote enhanced prostate cancer cell migration and metastasis.
This review outlines the role of RNase-L in antimicrobial immunity and the cytoskeleton-associated innate response. [review]
A 2.5 A and 3.25 A X-ray crystal and small-angle X-ray scattering structure of RNase L bound to a natural 2-5A activator with and without ADP or the nonhydrolysable ATP mimetic AMP (Montrer TMPRSS5 Anticorps)-PNP (Montrer NP Anticorps) is functionally characterized.
This gene encodes a component of the interferon-regulated 2-5A system that functions in the antiviral and antiproliferative roles of interferons. Mutations in this gene have been associated with predisposition to prostate cancer and this gene is a candidate for the hereditary prostate cancer 1 (HPC1) allele.
, 2-5A-dependent RNase
, 2-5A-dependent ribonuclease
, RNase L
, ribonuclease 4
, 2',5'-oligoisoadenylate synthetase-dependent
, interferon-induced 2-5A-dependent RNase