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EFHC1 Protein (Myc-DYKDDDDK Tag)

EFHC1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2719959
  • Antigène Voir toutes EFHC1 Protéines
    EFHC1 (EF-Hand Domain (C-terminal) Containing 1 (EFHC1))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette EFHC1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human EFHC1 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 EFHC1 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
    EFHC1 (EF-Hand Domain (C-terminal) Containing 1 (EFHC1))
    Autre désignation
    Efhc1 (EFHC1 Produits)
    Synonymes
    MGC63931 Protein, zgc:63931 Protein, MGC84469 Protein, MGC89313 Protein, dJ304B14.2 Protein, 1700029F22Rik Protein, mRib72-1 Protein, myoclonin1 Protein, EF-hand domain containing 1 Protein, EF-hand domain (C-terminal) containing 1 Protein, EF-hand domain (C-terminal) containing 1 L homeolog Protein, Efhc1 Protein, EFHC1 Protein, efhc1 Protein, efhc1.L Protein
    Sujet
    This gene encodes an EF-hand-containing calcium binding protein. The encoded protein likely plays a role in calcium homeostasis. Mutations in this gene have been associated with susceptibility to juvenile myoclonic epilepsy and juvenile absence epilepsy. Alternatively spliced transcript variants have been described.
    Poids moléculaire
    73.8 kDa
    NCBI Accession
    NP_060570
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