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DDB2 Antikörper

This anti-DDB2 antibody (ABIN7009799) is a Rabbit Polyclonal antibody detecting DDB2 in WB, IF. Suitable for Human, Mouse, Rat.
Produktnummer ABIN7009799

Quick Overview for DDB2 Antikörper (ABIN7009799)

Target

Alle DDB2 Antikörper anzeigen
DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))

Reaktivität

  • 43
  • 18
  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 44
  • 3
Kaninchen

Klonalität

  • 33
  • 14
Polyklonal

Konjugat

  • 29
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser DDB2 Antikörper ist unkonjugiert

Applikation

  • 29
  • 14
  • 10
  • 10
  • 7
  • 5
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein of human DDB2 (NP_000098.1).

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000 IF 1:50-1:200

    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

    DDB2 (Damage-Specific DNA Binding Protein 2, 48kDa (DDB2))

    Andere Bezeichnung

    DDB2

    Hintergrund

    This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene.

    Molekulargewicht

    Observed_MW: 48 kDa

    Calculated_MW: 17 kDa/26 kDa/40 kDa/47 kDa

    Gen-ID

    1643

    UniProt

    Q92466

    Pathways

    DNA Reparatur
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