Anti-Human/Mouse/Rat DDB1 Polyclonal Antibody

The protein encoded by this gene is the large subunit (p127) of the heterodimeric DNA damage-binding (DDB) complex while another protein (p48) forms the small subunit. This protein complex functions in nucleotide-excision repair and binds to DNA following UV damage. Defective activity of this complex causes the repair defect in patients with xeroderma pigmentosum complementation group E (XPE) - an autosomal recessive disorder characterized by photosensitivity and early onset of carcinomas. However, it remains for mutation analysis to demonstrate whether the defect in XPE patients is in this gene or the gene encoding the small subunit. In addition, Best vitelliform mascular dystrophy is mapped to the same region as this gene on 11q, but no sequence alternations of this gene are demonstrated in Best disease patients. The protein encoded by this gene also functions as an adaptor molecule for the cullin 4 (CUL4) ubiquitin E3 ligase complex by facilitating the binding of substrates to this complex and the ubiquitination of proteins.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA11370
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human DDB1
Specificity
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot Q16531
Concentration 0.1 mg/mL
Dilution WB 1:200-1:1000, IHC 1:10-1:100
Formulation
Application WB,IHC,ELISA
Other Names XPE, DDBA, XAP1, XPCE, XPE-BF, UV-DDB1
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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