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BHLHA9 Protein (Myc-DYKDDDDK Tag)

BHLHA9 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2715153
  • Antigène Voir toutes BHLHA9 Protéines
    BHLHA9 (Basic Helix-Loop-Helix Family, Member A9 (BHLHA9))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    Humain
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette BHLHA9 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Basic helix-loop-helix family, member a9 (BHLHA9). protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product BHLHA9 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
    25 mM Tris.HCl, pH 7.3, 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
    BHLHA9 (Basic Helix-Loop-Helix Family, Member A9 (BHLHA9))
    Abstract
    BHLHA9 Produits
    Synonymes
    A830053O21Rik Protein, BHLHF42 Protein, bhlhf42 Protein, wu:fb99e06 Protein, basic helix-loop-helix family, member a9 Protein, basic helix-loop-helix family member a9 Protein, Bhlha9 Protein, BHLHA9 Protein, bhlha9 Protein
    Sujet
    This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3).
    Poids moléculaire
    24 kDa
    NCBI Accession
    NP_001157877
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