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WRB anticorps

WRB Reactivité: Souris, Rat IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7262941
  • Antigène Voir toutes WRB Anticorps
    WRB (Tryptophan Rich Basic Protein (WRB))
    Reactivité
    • 13
    • 2
    • 1
    Souris, Rat
    Hôte
    • 8
    • 5
    • 1
    Lapin
    Clonalité
    • 12
    • 2
    Polyclonal
    Conjugué
    • 10
    • 2
    • 1
    • 1
    Cet anticorp WRB est non-conjugé
    Application
    • 10
    • 8
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human WRB (NP_004618.2).
    Isotype
    IgG
    Top Product
    Discover our top product WRB Anticorps primaire
  • Indications d'application
    IHC 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
    WRB (Tryptophan Rich Basic Protein (WRB))
    Autre désignation
    WRB (WRB Produits)
    Synonymes
    anticorps pwi, anticorps wu:ft06h05, anticorps zgc:101856, anticorps chd5, anticorps MGC89989, anticorps WRB, anticorps UCP-1, anticorps DKFZp469L094, anticorps wrb, anticorps mCHD5, anticorps MGC115192, anticorps CHD5, anticorps 5530402J05Rik, anticorps C030018G21Rik, anticorps Chd5, anticorps tryptophan rich basic protein, anticorps tryptophan rich basic protein L homeolog, anticorps WRB, anticorps wrb, anticorps wrb.L, anticorps Wrb
    Sujet
    This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    ID gène
    7485
    UniProt
    O00258
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