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Human Polyclonal ERCC4 Primary Antibody for ELISA, ICC - ABIN253150
Earley, Turchi: Interrogation of nucleotide excision repair capacity: impact on platinum-based cancer therapy. in Antioxidants & redox signaling 2011
Show all 2 Pubmed References
Human Monoclonal ERCC4 Primary Antibody for ELISA, ICC - ABIN451725
Paul, Nagano, Robaire: Aging results in differential regulation of DNA repair pathways in pachytene spermatocytes in the Brown Norway rat. in Biology of reproduction 2011
ERCC1 (show ERCC1 Antibodies) was not detectable in the nucleus of the XPF knockout cells indicating the necessity of a functional XPF/ERCC1 (show ERCC1 Antibodies) heterodimer to allow ERCC1 (show ERCC1 Antibodies) to enter the nucleus.
Strikingly, the addition of the single-stranded DNA (ssDNA)-binding replication protein A (RPA) selectively restores XPF-ERCC1 endonuclease activity on this structure. The 5'-3' exonuclease SNM1A can load from the XPF-ERCC1-RPA-induced incisions and digest past the crosslink to quantitatively complete the unhooking reaction.
Based on structural models, NMR titrations, DNA-binding studies, site-directed mutagenesis, charge distribution, and sequence conservation, we propose that the HhH (show SLC25A15 Antibodies) domain of ERCC1 (show ERCC1 Antibodies) binds to dsDNA upstream of the damage, and XPF binds to the non-damaged strand within a repair bubble
silenced XPF significantly increased the sensitivity and survival following treatment with cisplatin in xenograft mice bearing renal cell tumor.
Polymorphisms in XPF gene is associated with gastrointestinal stromal tumours.
inherited abnormalities in DNA repair pathway related to XPF 30028C and TP53 (show TP53 Antibodies) Arg72Pro polymorphisms act as prognostic factors for progression free survival and overall survival of cutaneous melanoma patients.
Based on these results, we conclude that the XPF gene polymorphism Ser835Ser may be associated with a decreased risk of colorectal cancer.
Polymorphisms of ERCC4 gene are associated with HPV-positive cervical cancer.
Helicobacter Pylori introduces double-stranded DNA breaks by the nucleotide excision repair endonucleases XPF and XPG (show ERCC5 Antibodies), which, together with RelA (show NFkBP65 Antibodies), are recruited to chromatin in a highly coordinated, type IV secretion system-dependent manner.
SLX4 (FANCP (show BTBD12 Antibodies)) and XPF (FANCQ) proteins interact with each other and play a vital role in the Fanconi anemia (show PALB2 Antibodies) (FA) DNA repair pathway.
ERCC1 (show ERCC1 Antibodies)-XPF cooperates with CTCF (show CTCF Antibodies) and cohesin to facilitate the developmental silencing of imprinted genes and that persistent DNA damage triggers chromatin changes that affect gene expression programs associated with NER (show NR1H2 Antibodies) disorders.
these results establish USP45 as a new regulator of XPF-ERCC1 (show ERCC1 Antibodies) crucial for efficient DNA repair
SLX4 (show BTBD12 Antibodies) is a tumor suppressor, which activates XPF-ERCC1 (show ERCC1 Antibodies) nuclease (show DCLRE1C Antibodies) specificity in DNA crosslink repair.
Data reveal an unanticipated involvement of the ERCC1 (show ERCC1 Antibodies)/XPF NER (show NR1H2 Antibodies) endonuclease in the regulation of telomere integrity.
mitomycin C triggered sister chromatid exchanges in wild-type cells but chromatid fusions in Ercc1 (show ERCC1 Antibodies)(-/-) and Xpf mutant cells, indicating that in their absence, repair of double-strand breaks(DSBs)is prevented.
In mice with overexpressed TRF2 (show TERF2 Antibodies), telomere loss is mediated by Xpf.
These data support the conclusion that, as in yeast, ERCC1 (show ERCC1 Antibodies)-XPF facilitates double-strand breaks repair via an end-joining mechanism that is Ku86 (show XRCC5 Antibodies) independent.
These data support a model in which the interstrand crosslink repair-specific function of XPF-ERCC1 is dependent on recruitment, positioning and substrate recognition.
The protein encoded by this gene forms a complex with ERCC1 and is involved in the 5' incision made during nucleotide excision repair. This complex is a structure specific DNA repair endonuclease that interacts with EME1. Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F), or xeroderma pigmentosum VI (XP6).
DNA excision repair protein ERCC-4
, DNA repair endonuclease XPF
, DNA repair protein complementing XP-F cells
, excision-repair, complementing defective, in Chinese hamster
, xeroderma pigmentosum group F-complementing protein
, xeroderma pigmentosum, complementation group F
, DNA repair endonuclease subunit
, Ercc4 protein-like
, excision repair cross-complementing rodent repair deficiency, complementation group 4
, DNA repair endonuclease XPF-like