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PABPC5 anticorps

PABPC5 Reactivité: Humain, Souris WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6572120
  • Antigène Voir toutes PABPC5 Anticorps
    PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))
    Reactivité
    • 18
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 16
    • 2
    Lapin
    Clonalité
    • 18
    Polyclonal
    Conjugué
    • 11
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PABPC5 est non-conjugé
    Application
    • 11
    • 5
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human PABPC5
    Isotype
    IgG
    Top Product
    Discover our top product PABPC5 Anticorps primaire
  • Indications d'application
    WB 1:1000 - 1:4000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    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
    PABPC5 (Poly(A) Binding Protein, Cytoplasmic 5 (PABPC5))
    Autre désignation
    PABPC5 (PABPC5 Produits)
    Synonymes
    anticorps PABPC5, anticorps PABP5, anticorps C820015E17, anticorps poly(A) binding protein cytoplasmic 5, anticorps poly A binding protein, cytoplasmic 5, anticorps poly(A) binding protein, cytoplasmic 5, anticorps PABPC5, anticorps Pabpc5
    Sujet

    Synonyms: PABP5,Poly(A) binding protein 5,Poly(A) binding protein cytoplasmic 5,Polyadenylate binding protein 5

    Background: This gene encodes a protein that binds to the polyA tail found at the 3' end of most eukaryotic mRNAs. It is thought to play a role in the regulation of mRNA metabolic processes in the cytoplasm. This gene is located in a gene-poor region within the X-specific 13d-sY43 subinterval of the chromosome Xq21.3/Yp11.2 homology block. It is located close to translocation breakpoints associated with premature ovarian failure, and is therefore a potential candidate gene for this disorder.

    Poids moléculaire

    Observed_MW: 43kDa

    Calculated_MW: 39kDa/43kDa

    ID gène
    140886
    UniProt
    Q96DU9
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