DDB1 anticorps

N° du produit ABIN7467425

Cet anticorps anti-DDB1 est un anticorps Lapin Polyclonal détectant DDB1 dans WB. Adapté pour Humain.

Aperçu rapide pour DDB1 anticorps (ABIN7467425)

Antigène: DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DDB1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-DDB1 anticorps

Réactivité croisée: Humain, Souris, Rat

Purification: Affinity purified with antigen

Immunogène: Synthetic peptide conugated to protein carrier.

Isotype: IgG

Information d'application

Indications d'application: For WB: Use at an assay dependent dilution. Predicted molecular weight: 127 kDa. Optimal dilutions/concentrations should be determined by the researcher.

Commentaires:

Positive Control: T47D and MCF-7 whole cell lysate

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS pH 7.2, No Preservative

Agent conservateur: Without preservative

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur DDB1

Antigène: DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

Autre désignation: damage specific DNA binding protein 1

Sujet: Damage specific DNA binding protein 1 , DDBA , UV-DDB1 , XAP1 , XPCE , XPE , XPE-BF,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. [provided by RefSeq, May 2012]

Poids moléculaire: 127 kDa

ID gène: 1642

UniProt: Q16531

Pathways: Réparation de l'ADN