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anti-Human XRCC4 Antikörper:
anti-Mouse (Murine) XRCC4 Antikörper:
anti-Rat (Rattus) XRCC4 Antikörper:
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Human Polyclonal XRCC4 Primary Antibody für IHC - ABIN967265
Li, Otevrel, Gao, Cheng, Seed, Stamato, Taccioli, Alt: The XRCC4 gene encodes a novel protein involved in DNA double-strand break repair and V(D)J recombination. in Cell 1996
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Human Monoclonal XRCC4 Primary Antibody für IF, WB - ABIN968566
Gao, Sun, Frank, Dikkes, Fujiwara, Seidl, Sekiguchi, Rathbun, Swat, Wang, Bronson, Malynn, Bryans, Zhu, Chaudhuri, Davidson, Ferrini, Stamato, Orkin, Greenberg, Alt: A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis. in Cell 1999
Show all 3 Pubmed References
Human Polyclonal XRCC4 Primary Antibody für IHC - ABIN967264
Leber, Wise, Mizuta, Meek: The XRCC4 gene product is a target for and interacts with the DNA-dependent protein kinase. in The Journal of biological chemistry 1998
Show all 5 Pubmed References
Human Polyclonal XRCC4 Primary Antibody für ICC, IF - ABIN4366467
Stadler, Rexhepaj, Singan, Murphy, Pepperkok, Uhlén, Simpson, Lundberg: Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. in Nature methods 2013
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Mouse (Murine) Polyclonal XRCC4 Primary Antibody für IHC, WB - ABIN3022382
Dong, Wang, Wang, Zhang, Zhu, Gao, Yang, Qin, Liang, Chen, Deng, Ning, Liang, Gao, Xu: A stress-induced cellular aging model with postnatal neural stem cells. in Cell death & disease 2014
Human Polyclonal XRCC4 Primary Antibody für IF, IHC (p) - ABIN1327721
Enervald, Du, Visnes, Björkman, Lindgren, Wincent, Borck, Colleaux, Cormier-Daire, van Gent, Pie, Puisac, de Miranda, Kracker, Hammarström, de Villartay, Durandy, Schoumans, Ström, Pan-Hammarström: A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination. in The Journal of experimental medicine 2013
Human Polyclonal XRCC4 Primary Antibody für ICC, IF - ABIN440923
van Sluis, McStay: A localized nucleolar DNA damage response facilitates recruitment of the homology-directed repair machinery independent of cell cycle stage. in Genes & development 2015
XRCC4 has a negative role in Agrobacterium T-DNA integration.
This study demonstrated both ligase IV and XRCC4 may act in concert to modulate the development of glioma.
Data suggest that genetic variants of XRCC4 and ERCC1 (zeige ERCC1 Antikörper) may independently or jointly affect survival in chemotherapy-treated gastric cancer (GCa (zeige NPR1 Antikörper)) patients by modulating the gene expression in the tumors.
In a recombinant PNKP (zeige PNKP Antikörper)-XRCC4-LigIV complex, stable binding of PNKP (zeige PNKP Antikörper) requires XRCC4 phosphorylation. Only one PNKP (zeige PNKP Antikörper) protomer binds per XRCC4 dimer. Both the PNKP (zeige PNKP Antikörper) FHA (zeige CRY2 Antikörper) and catalytic domains contact the XRCC4 coiled-coil and LigIV BRCT repeats. Multipoint contacts between PNKP (zeige PNKP Antikörper) and XRCC4-LigIV regulate PNKP (zeige PNKP Antikörper) recruitment and activity within NHEJ.
Data suggest that stimulation of Artemis nuclease/DCLRE1C (zeige DCLRE1C Antikörper) activity by XRCC4-DNA ligase IV (zeige LIG4 Antikörper) hetero-complex and efficiency of blunt-end ligation are determined by structural configurations at the DNA ends. (XRCC4 = X-ray repair cross complementing 4)
involvement of ZNF281 (zeige ZNF281 Antikörper) in the cellular response to genotoxic stress through the control exercised on the expression of genes that act in different repair mechanisms
the various XRCC4 mutations that lead to primordial dwarfism and their impact on non-homologous end joining and V(D)J recombination are discussed (Review)
XRCC4 expression might have an influence on results of radiotherapy for patients with esophageal squamous cell carcinoma.
uterine cervical cancer patients with high Ku86 (zeige XRCC5 Antikörper) and XRCC4 expression had a significantly lower 5-year metastasis-free rate than others.
Frequencies of XRCC4-1394 T/G+G/G genotypes were higher in patients (%34) than the controls (%18.7). The statistical analysis revealed that the individuals who had XRCC4-1394 T/G+G/G genotype had an increased risk for autism spectrum disorder (OR = 2.23, 95% CI = 1.10-4.55)
Genetic Variations in XRCC4 (rs1805377) is not Associated with Hepatocellular Carcinoma in Thai Patients with Hepatitis B Virus Infection.
We find that non-canonical HR termination can occur in the absence of the classical non-homologous end joining gene XRCC4. We observe obligatory use of microhomology (MH)-mediated end joining and/or nucleotide addition during rejoining with the second end of the break
Data show that combined deletion of X-ray repair cross-complementing protein 4 (Xrcc4) and tumor suppressor p53 (Trp53 (zeige TP53 Antikörper)) predisposes B cells to lymphomagenesis.
FBXW7 (zeige FBXW7 Antikörper) facilitates nonhomologous end-joining via K63-linked polyubiquitylation of XRCC4 in tumor cells.
The present results collectively indicated that Lys271, but not Lys210, of XRCC4 is required for the nuclear localization of XRCC4 and LIG4 (zeige LIG4 Antikörper) and that the nuclear localizing ability is essential for DSB repair function of XRCC4.
DNA-PK and ATM (zeige ATM Antikörper) acts in parallel upstream of XRCC4, regulating through phosphorylation
XRCC4 C-terminal point mutants, R325F and N326L, are functionally deficient in terms of cell survival after irradiation.
These results establish that nonrecurrent CNVs can be, and frequently are, formed by mechanisms other than Xrcc4-dependent NHEJ.
analysis of the association of radiation-induced XRCC4 with chromatin DNA, by biochemical fractionation
conditional inactivation of the XRCC4 in nestin (zeige NES Antikörper)-expressing neuronal progenitor cells, although leading to no obvious phenotype in a WT background, leads to early onset of neuronally differentiated medulloblastomas (MBs (zeige NEU2 Antikörper)) in a p53 (zeige TP53 Antikörper)-deficient background
The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand break by non-homologous end joining and the completion of V(D)J recombination events. The non-homologous end-joining pathway is required both for normal development and for suppression of tumors. This gene functionally complements XR-1 Chinese hamster ovary cell mutant, which is impaired in DNA double-strand breaks produced by ionizing radiation and restriction enzymes. Alternative transcription initiation and alternative splicing generates several transcript variants.
DNA repair protein XRCC4
, X-ray repair complementing defective repair in Chinese hamster cells 4
, DNA-repair protein XRCC4
, X-ray repair cross complementing protein 4
, X-ray repair cross-complementing protein 4
, X-ray repair, complementing defective, repair in Chinese hamster