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RBM10 Protein (DYKDDDDK Tag)

RBM10 Origine: Humain Hôte: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2730603
  • Antigène Voir toutes RBM10 Protéines
    RBM10 (RNA Binding Motif Protein 10 (RBM10))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    Insect cells (Sf9)
    Purification/Conjugué
    Cette RBM10 protéine est marqué à la DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human RBM10 (full length, C-term DDK tag, transcript variant 1) protein expressed in Sf9 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product RBM10 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    50 mM Tris-HCl, pH 8.0, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    RBM10 (RNA Binding Motif Protein 10 (RBM10))
    Autre désignation
    Rbm10 (RBM10 Produits)
    Synonymes
    RBM10 Protein, DXS8237E Protein, GPATC9 Protein, GPATCH9 Protein, S1-1 Protein, TARPS Protein, ZRANB5 Protein, E430039K10Rik Protein, RNA binding motif protein 10 Protein, RBM10 Protein, rbm10 Protein, Rbm10 Protein
    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.[provided by RefSeq, Mar 2011]
    Poids moléculaire
    103.4 kDa
    NCBI Accession
    NP_005667
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