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DDB1 Antikörper

Der Kaninchen Polyklonal Anti-DDB1-Antikörper wurde für WB validiert. Er ist geeignet, DDB1 in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN7260875

Kurzübersicht für DDB1 Antikörper (ABIN7260875)

Target

Alle DDB1 Antikörper anzeigen
DDB1 (Damage Specific DNA Binding Protein 1 (DDB1))

Reaktivität

  • 46
  • 24
  • 20
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 37
  • 8
  • 1
Kaninchen

Klonalität

  • 35
  • 11
Polyklonal

Konjugat

  • 35
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DDB1 Antikörper ist unkonjugiert

Applikation

  • 31
  • 16
  • 15
  • 15
  • 11
  • 10
  • 9
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    A synthetic peptide of human DDB1 (NP_001914.3).

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

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

    Andere Bezeichnung

    DDB1

    Hintergrund

    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.

    Molekulargewicht

    Observed_MW: 127 kDa

    Calculated_MW: 50 kDa/126 kDa

    Gen-ID

    1642

    UniProt

    Q16531

    Pathways

    DNA Reparatur
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