DDB1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-12364
宿主: Rabbit
反应性: H,M,R
应用: WB,IHC
Overview
| Synonyms | Damage specific DNA binding protein 1,Damage-specific DNA-binding protein 1,DDB 1,DDB p127 subunit,Ddb1,DDB1,DDBa,DNA damage binding protein 1,DNA damage-binding protein 1,DNA damage-binding protein a,HBV X-associated protein 1,UV damaged DNA binding factor,UV damaged DNA binding protein 1,UV DDB 1,UV DDB1,UV-damaged DNA-binding factor,UV-damaged DNA-binding protein 1,UV-DDB 1,X associated protein 1,XAP 1,XAP-1,XAP1,Xeroderma pigmentosum group E complementing protein,Xeroderma pigmentosum group E-complementing protein,XPCe,XPE,XPE BF,XPE binding factor,XPE-BF,XPE-binding factor,DDB1抗体 |
| Swissprot | Q16531 |
| Source | Rabbit |
| Reactivity | Human,Mouse,Rat |
| Immunogen | Synthetic peptide of human DDB1 |
| Application | WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213) |
| Recommended dilution | WB,,1:200-1:500; |
| Concentration | 0.3 mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Cytoplasm. Nucleus. Primarily cytoplasmic. Translocates to the nucleus following UV irradiation and subsequently accumulates at sites of DNA damage. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
| 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. |
