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DDI2 anticorps

L’anticorps Lapin Polyclonal anti-DDI2 a été validé pour ELISA, WB et IHC. Il convient pour détecter DDI2 dans des échantillons de Humain et Souris.
N° du produit ABIN7246202

Aperçu rapide pour DDI2 anticorps (ABIN7246202)

Antigène

Voir toutes DDI2 Anticorps
DDI2 (DNA-Damage Inducible 1 Homolog 2 (DDI2))

Reactivité

Humain, Souris

Hôte

  • 23
Lapin

Clonalité

  • 23
Polyclonal

Conjugué

  • 7
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DDI2 est non-conjugé

Application

  • 12
  • 11
  • 2
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human DDI2

    Isotype

    IgG
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.32 mg/mL

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

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

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

    Autre désignation

    DDI2

    Sujet

    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.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 45 kDa

    UniProt

    Q5TDH0
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