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SOX14 Protein (Myc-DYKDDDDK Tag)

SOX14 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2732432
  • Antigène Voir toutes SOX14 Protéines
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 5
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette SOX14 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human SOX14 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 SOX14 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
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    Autre désignation
    Sox14 (SOX14 Produits)
    Synonymes
    SOX28 Protein, zgc:123197 Protein, SRY-box 14 Protein, SRY-box 14 S homeolog Protein, SRY box 14 Protein, SRY (sex determining region Y)-box 14 Protein, SOX14 Protein, sox14.S Protein, Sox14 Protein, sox14 Protein
    Sujet
    This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.
    Poids moléculaire
    26.3 kDa
    NCBI Accession
    NP_004180
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