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RBM10 anticorps

RBM10 Reactivité: Humain, Souris, Rat ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246700
  • Antigène Voir toutes RBM10 Anticorps
    RBM10 (RNA Binding Motif Protein 10 (RBM10))
    Reactivité
    • 38
    • 13
    • 11
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    Humain, Souris, Rat
    Hôte
    • 37
    • 2
    Lapin
    Clonalité
    • 37
    • 2
    Polyclonal
    Conjugué
    • 19
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp RBM10 est non-conjugé
    Application
    • 26
    • 20
    • 8
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human RBM10
    Isotype
    IgG
    Top Product
    Discover our top product RBM10 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.96 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
    RBM10 (RNA Binding Motif Protein 10 (RBM10))
    Autre désignation
    RBM10 (RBM10 Produits)
    Synonymes
    anticorps RBM10, anticorps DXS8237E, anticorps GPATC9, anticorps GPATCH9, anticorps S1-1, anticorps TARPS, anticorps ZRANB5, anticorps E430039K10Rik, anticorps RNA binding motif protein 10, anticorps RBM10, anticorps rbm10, anticorps Rbm10
    Sujet
    This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.
    UniProt
    P98175
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