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ITT1615

ITT1615
ITT1615-2
ITT1615
ITT1615-2
ITT1615
  • Gene/Protein: ERCC4
  • Product Description: Immunotag™ ERCC4 Polyclonal Antibody
280.0000
Price in reward points: 294

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Immunotag™ ERCC4 Polyclonal Antibody
Antibody Specification
Datasheet
Target Protein ERCC4
Clonality Polyclonal
Storage/Stability -20°C/1 year
Application WB,ELISA
Recommended Dilution Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Concentration 1 mg/ml
Reactive Species Human,Mouse
Host Species Rabbit
Immunogen The antiserum was produced against synthesized peptide derived from human XPF. AA range:801-850
Specificity ERCC4 Polyclonal Antibody detects endogenous levels of ERCC4 protein.
Purification The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
Form Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Gene Name ERCC4
Accession No. Q92889 Q9QZD4
Alternate Names ERCC4; ERCC11; XPF; DNA repair endonuclease XPF; DNA excision repair protein ERCC-4; DNA repair protein complementing XP-F cells; Xeroderma pigmentosum group F-complementing protein
Description ERCC excision repair 4, endonuclease catalytic subunit(ERCC4) Homo sapiens 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).[provided by RefSeq, Mar 2009],
Cell Pathway/ Category Nucleotide excision repair,
Protein Expression Epithelium,Fibroblast,
Subcellular Localization nucleotide-excision repair complex,nucleotide-excision repair factor 1 complex,chromosome, telomeric region,nuclear chromosome, telomeric region,nucleus,nucleoplasm,transcription factor TFIID complex,ERCC4-ERCC1 complex,
Protein Function cofactor:Magnesium.,disease:Defects in ERCC4 are a cause of XFE progeroid syndrome [MIM:610965]. This syndrome is illustrated by one patient who presented with dwarfism, cachexia and microcephaly.,disease:Defects in ERCC4 are the cause of xeroderma pigmentosum complementation group F (XP-F) [MIM:278760]; also known as xeroderma pigmentosum VI (XP6). XP-F is an autosomal recessive disease characterized by hypersensitivity of the skin to sunlight followed by high incidence of skin cancer and frequent neurologic abnormalities.,function:Structure-specific DNA repair endonuclease responsible for the 5-prime incision during DNA repair. Involved in homologous recombination that assists in removing interstrand cross-link.,similarity:Belongs to the XPF family.,subunit:Heterodimer composed of ERCC1 and XPF/ERCC4. Interacts with EME1.,
Usage For Research Use Only! Not for diagnostic or therapeutic procedures.
Material Safety Data Sheet
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