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Human Polyclonal DDX39 Primary Antibody für ELISA, WB - ABIN563499
Banerjee, Sammarco, Ditch, Grabczyk: A dual reporter approach to quantify defects in messenger RNA processing. in Analytical biochemistry 2009
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Cow (Bovine) Polyclonal DDX39 Primary Antibody für WB - ABIN2775195
Allcock, Williams, Price: The central MHC gene, BAT1, may encode a protein that down-regulates cytokine production. in Genes to cells : devoted to molecular & cellular mechanisms 2001
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Human Polyclonal DDX39 Primary Antibody für FACS, IHC (p) - ABIN1881102
Choudhary, Kumar, Gnad, Nielsen, Rehman, Walther, Olsen, Mann: Lysine acetylation targets protein complexes and co-regulates major cellular functions. in Science (New York, N.Y.) 2009
RNA helicase (zeige DDX46 Antikörper) Ddx39 is expressed in the developing central nervous system, limb, otic vesicle, branchial arches and facial mesenchyme of Xenopus laevis.
The expression of DDX39 in gemcitabine-sensitive KLM1 and -resistant KLM1-R cells was compared.
Mx proteins exert their antiviral activity against IAV by interfering with the function of the RNA helicases UAP56 (zeige DDX39B Antikörper) and URH49
Regulation of URH49 mRNA expression and comparison with the related UAP56 (zeige DDX39B Antikörper) RNA helicase (zeige DHX9 Antikörper).
Study showed that a genetic variant in the 5' UTR (zeige UTS2R Antikörper) of DDX39B reduces translation of DDX39B mRNAs and increases multiple sclerosis (MS) risk. Importantly, this DDX39B variant showed strong genetic & functional epistasis with allelic variants in IL7R (zeige IL7R Antikörper) exon 6; study establishes the occurrence of biological epistasis in humans & provides mechanistic insight into the regulation of IL7R (zeige IL7R Antikörper) exon 6 splicing & its impact on MS risk.
DDX39B and its paralog DDX39A regulate androgen receptor (zeige AR Antikörper) splice variant AR-V7 generation
Distinct features of RNA influence and ATPase (zeige DNAH8 Antikörper) efficiency between UAP56 (zeige DDX39B Antikörper) and TcSub2 may reflect distinct structures for functional sites of TcSub2. For this reason, ligand-based or structure-based methodologies can be applied to investigate the potential of TcSub2 as a target for new drugs.
However, no significant association was observed between the DDX39B -22 G/C polymorphism in the cases and controls. Furthermore, it is clarified that the protective effect of IL-4 (zeige IL4 Antikörper) -590 is independent from APOE (zeige APOE Antikörper) protective genotypes
The G allele of DDX39B-22C > G was associated with absent or decreased manifestations of vivax malaria and the C allele was a risk factor for disease complications.
We unravel the role of unexplored immunologically important genes, BAT1 and BTNL2 (zeige BTNL2 Antikörper), and the haplotypes of the significantly associated SNPs therein, to understand susceptibility to the disease, leprosy and its differential severity.
these data identify UAP56 (zeige DDX39B Antikörper) as an important binding partner of Bcr (zeige BCR Antikörper) and a novel target for inhibiting vascular smooth muscle cell proliferation.
UAP56 (zeige DDX39B Antikörper) and URH49 exhibit an intrinsic CRM1 (zeige XPO1 Antikörper)-independent nucleocytoplasmic shuttling
In summary, these data demonstrate that UAP56 (zeige DDX39B Antikörper) is utilized by influenza A viruses to prevent the formation of dsRNA and, hence, the activation of the innate immune response.
This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene.
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39
, nuclear RNA helicase
, ATP-dependent RNA helicase DDX39
, ATP-dependent RNA helicase DDX39A
, DEAD box protein 39
, DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 39
, UAP56-related helicase, 49 kDa
, HLA-B associated transcript 1
, 56 kDa U2AF65-associated protein
, ATP-dependent RNA helicase p47
, HLA-B-associated transcript 1 protein
, nuclear RNA helicase (DEAD family)
, spliceosome RNA helicase BAT1
, spliceosome RNA helicase DDX39B
, DEAD box protein UAP56
, DEADD box protein
, HLA-B associated transcript 1A
, HLA-B-associated transcript 1A
, Nuclear RNA helicase
, spliceosome RNA helicase Bat1
, spliceosome RNA helicase Ddx39b