DDB1 antibody

Synonyms:DDB p127 subunit antibody, DDB1 antibody, DDBA antibody, DNA damage binding protein 1 antibody, DNA damage binding protein a antibody, HBV X associated protein 1 antibody, UV damaged DNA binding factor antibody, UV DDB 1 antibody, UV antibody
Catalogue No.:FNab02284Reactivity:Human, Mouse, Rat
Host:RabbitTested Application:ELISA, WB, IHC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
DDB1 antibody
Catalogue No.
FNab02284
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
damage-specific DNA binding protein 1, 127kDa
Alternative Names
DDB p127 subunit antibody, DDB1 antibody, DDBA antibody, DNA damage binding protein 1 antibody, DNA damage binding protein a antibody, HBV X associated protein 1 antibody, UV damaged DNA binding factor antibody, UV DDB 1 antibody, UV antibody
UniProt ID
Q16531
Observed MW
127 kDa
Application
Tested Applications
ELISA, WB, IHC
Recommended dilution
WB: 1:500 - 1:1000; IHC: 1:50 - 1:100
Validated Images
mouse testis tissue were subjected to SDS PAGE followed by western blot with FNab02284(DDB1 antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human liver using FNab02284(DDB1 antibody) at dilution of 1:50
Background
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.