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DDX39B anticorps

Cet anticorps anti-DDX39B est un anticorps Lapin Polyclonal détectant DDX39B dans IHC et IF. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7264385

Aperçu rapide pour DDX39B anticorps (ABIN7264385)

Antigène

Voir toutes DDX39B Anticorps
DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

Reactivité

  • 33
  • 8
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 28
  • 5
Lapin

Clonalité

  • 26
  • 7
Polyclonal

Conjugué

  • 16
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DDX39B est non-conjugé

Application

  • 23
  • 17
  • 16
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human DDX39B (NP_004631.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:100-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

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

    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

    DDX39B (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39B (DDX39B))

    Autre désignation

    DDX39B

    Sujet

    This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13 kDa, V1 subunit G2) gene.

    ID gène

    7919

    UniProt

    Q13838

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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