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DDI2 Antikörper

Der Kaninchen Polyklonal Anti-DDI2-Antikörper wurde für ELISA, WB und IHC validiert. Er ist geeignet, DDI2 in Proben von Human und Maus zu detektieren.
Produktnummer ABIN7246202

Kurzübersicht für DDI2 Antikörper (ABIN7246202)

Target

Alle DDI2 Antikörper anzeigen
DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

Reaktivität

Human, Maus

Wirt

  • 24
Kaninchen

Klonalität

  • 24
Polyklonal

Konjugat

  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DDI2 Antikörper ist unkonjugiert

Applikation

  • 13
  • 12
  • 2
  • 2
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Fusion protein of human DDI2

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1.32 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

    Andere Bezeichnung

    DDI2

    Hintergrund

    DDI1 and DDI2 are ubiquitin receptor homologs of the Saccharomyces cerevisiae ddi1 protein, which is involved in regulation of the cell cycle and the late secretory pathway. DDI2 is a 399 amino acid protein that contains one ubiquitin-like domain and exists as three isoforms as a result of alternative splicing. The gene encoding DDI2 maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.

    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 45 kDa

    UniProt

    Q5TDH0
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