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DDB1 Antikörper

This anti-DDB1 antibody (ABIN7260707) is a Rabbit Polyclonal antibody detecting DDB1 in IHC, IF. Suitable for Human, Mouse, Rat.
Produktnummer ABIN7260707

Quick Overview for DDB1 Antikörper (ABIN7260707)

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

  • 32
  • 15
  • 15
  • 14
  • 11
  • 10
  • 9
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    A synthetic peptide of human DDB1

    Isotyp

    IgG
  • Applikationshinweise

    IHC 1:50-1:100 IF 1:50-1:100

    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.

    Gen-ID

    1642

    UniProt

    Q16531

    Pathways

    DNA Reparatur
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