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DCDC2 Protein (Myc-DYKDDDDK Tag)

DCDC2 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2719244
  • Antigène Voir toutes DCDC2 Protéines
    DCDC2 (Doublecortin Domain Containing 2 (DCDC2))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 2
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette DCDC2 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human DCDC2 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 DCDC2 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
    DCDC2 (Doublecortin Domain Containing 2 (DCDC2))
    Autre désignation
    Dcdc2 (DCDC2 Produits)
    Synonymes
    DCDC2A Protein, RU2 Protein, RU2S Protein, DCDC2 Protein, zgc:123267 Protein, doublecortin domain containing 2 Protein, doublecortin domain containing 2B Protein, DCDC2 Protein, Dcdc2 Protein, dcdc2b Protein
    Sujet
    This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
    Poids moléculaire
    52.7 kDa
    NCBI Accession
    NP_057440
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