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anti-Human XRCC3 Antibodies:
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Human Polyclonal XRCC3 Primary Antibody for IP, WB - ABIN151186
Yoshihara, Ishida, Kinomura, Katsura, Tsuruga, Tashiro, Asahara, Miyagawa: XRCC3 deficiency results in a defect in recombination and increased endoreduplication in human cells. in The EMBO journal 2004
Show all 12 Pubmed References
Human Monoclonal XRCC3 Primary Antibody for ICC, IF - ABIN151307
Forget, Bennett, Knight: Xrcc3 is recruited to DNA double strand breaks early and independent of Rad51. in Journal of cellular biochemistry 2004
Show all 10 Pubmed References
Monoclonal XRCC3 Primary Antibody for WB - ABIN534116
Compton, Choi, Cesare, Ozgür, Griffith: Xrcc3 and Nbs1 are required for the production of extrachromosomal telomeric circles in human alternative lengthening of telomere cells. in Cancer research 2007
Show all 5 Pubmed References
Polyclonal XRCC3 Primary Antibody for WB - ABIN540236
Szüts, Simpson, Kabani, Yamazoe, Sale: Role for RAD18 in homologous recombination in DT40 cells. in Molecular and cellular biology 2006
Show all 4 Pubmed References
Human Polyclonal XRCC3 Primary Antibody for IHC, WB - ABIN6673450
Zhang, Tang, Jiang, Mao: The transcription factor GATA3 is required for homologous recombination repair by regulating CtIP expression. in Oncogene 2017
Show all 2 Pubmed References
Mouse (Murine) Polyclonal XRCC3 Primary Antibody for IHC, WB - ABIN3023006
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
Show all 2 Pubmed References
Results indicated that,the rs12432907 of XRCC3 carrying T allele, the rs144848 of BRCA2 with C allele and the rs1805800 of NBS1 with genotype(TT) of individuals were associated with lower genetic damage, while the rs2295152 of XRCC3 carrying T allele, the rs13312986 (CC and CT genotypes) and the rs2697679 of NBS1 with A allele were associated with higher genetic damage in workers exposed to chromate.
XRCC3 Thr241Met gene polymorphism in Asian population was associated with osteosarcoma risk, but XRCC3 Thr241Met CC genotype was not associated with Enneking stage, tumor location, and tumor metastasis. [meta-analysis]
A direct role of XRCC3 in maintaining mtDNA integrity under replication stress conditions.XRCC3 binds to mtDNA control regions along with POLG.
According to the results obtained the rs1544410 AA genotype (VDR gene) and the presence of less than 20 CAG repeats in the 1st exon (AR gene) are the risk factors for the development of prostate cancer. The het- erozygous genotype 722 CT (XRCC3 gene) demonstrated the protective effect.
Low XRCC3 rs861539 T allele is associated with breast Cancer.
Although XRCC3 plays a role in asthma etiology, the variant XRCC3 genotypes do not serve as practicable predictive markers for asthma risk in Taiwanese.
Our present case-control study has shown that tryptophan allele (R/W-W/W genotype) in XRCC1A (Arg194Trp) gene significantly increased the risk of breast cancer 1.44-fold..the present case-control study did not reveal any significant association of XRCC3 (Thr241Met) polymorphism with the risk of breast cancer in females from NE region of India
Our results indicated a link between ERCC1 rs3212986 and the onset of late gastrointestinal toxicity ..No association was found regarding the XRCC3 rs861539 polymorphism and any clinical toxicity event
XRCC3 gene SNPs could influence the tumour aggressiveness expressed by tumour grade in hepatocellular carcinoma.
XRCC3 deleterious variants were identified in breast and ovarian cancer cases.
DNA sequencing was performed for six single-nucleotide polymorphisms in the GSTP1, RAD51, XRCC1 and XRCC3 genes in BC patients and the control group. Two variants in the 5'-UTR of the XRCC3 and RAD51 genes showed a significant association with susceptibility to breast cancer. Additionally, authors reported 2 mutations in intron 7 of the XRCC3 gene.
results indicate XRCC3 Thr241Met and TYMS 5'-UTR VNTR polymorphisms are associated with time-to-metastasis, and may have potential biological roles in expediting the metastatic process
hypermethylation of homologous recombination DNA repair genes including RAD51B and XRCC3 is associated with an inflamed phenotype in squamous cell cancers of the head and neck, lung and cervix.
Study suggested that RAD51, XRCC1, and XRCC3 polymorphisms may be predictive factors for radiation-induced acute toxicity in rectal cancer patients treated with preoperative combined therapy.
XRCC1 Arg399Gln Gln/Gln genotype, Gln allele, and homozygote variants of XRCC3 Thr241Met polymorphism may be a risk factor for predisposition of Oral Squamous Cell Carcinoma in Turkish. In addition, XRCC3 Thr241Met genotype could be associated with tumor size and level of daily smoking.
The combined AA/AA genotype and GG/GA genotype frequencies for rs1799794 and rs709399 polymorphisms were significantly higher in thyroid cancer patients compared to control group when compared with combined AA/GG genotype as reference.
the association of six non-synonymous coding variants from XRCC1, XRCC3 and XPD genes with hepatocellular carcinoma risk, was assessed.
The analysis results showed that the following polymorphisms were correlated with susceptibility to lung cancer: rs4646903 in CYP1A1 (P < 0.001), rs1048943 in CYP1A1 (P < 0.001), rs1695 in GSTP1 (P < 0.05), rs13181 in ERCC2 (P < 0.001), and rs25487 in XRCC1 (P < 0.05); no such correlation existed in rs861539 in XRCC3 (P > 0.05).
based on the evidence from the large-scale case-control study and meta-analysis, the rs861539 within XRCC3 gene was associated with the risk of NPC under recessive model.
our study suggested that the polymorphism of rs861539 in XRCC3 was associated with increased risk of PTC.
the RAD51C-XRCC3-associated Holliday junction resolvase complex associates with crossovers and may play an essential role in the resolution of recombination intermediates prior to chromosome segregation
This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene functionally complements Chinese hamster irs1SF, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents and is chromosomally unstable. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. Alternatively spliced transcript variants encoding the same protein have been identified.
DNA repair protein XRCC3
, X-ray repair cross-complementing protein 3
, X-ray repair complementing defective repair in Chinese hamster cells 3
, DNA-repair protein XRCC3