Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

HLCS Protein (Myc-DYKDDDDK Tag)

HLCS Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2715276
  • Antigène Voir toutes HLCS Protéines
    HLCS (Biotin-Protein Ligase (HLCS))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette HLCS protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Biotin-protein ligase / HLCS 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 HLCS 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
    HLCS (Biotin-Protein Ligase (HLCS))
    Autre désignation
    Biotin-Protein Ligase,hlcs (HLCS Produits)
    Synonymes
    410I21.SP6 Protein, D16Jhu34 Protein, HCS Protein, RGD1565360 Protein, holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) Protein, holocarboxylase synthetase Protein, Hlcs Protein, HLCS Protein
    Sujet
    This gene encodes an enzyme that catalyzes the binding of biotin to carboxylases and histones. The protein plays an important role in gluconeogenesis, fatty acid synthesis and branched chain amino acid catabolism. Defects in this gene are the cause of holocarboxylase synthetase deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jun 2011].
    Poids moléculaire
    80.6 kDa
    NCBI Accession
    NP_000402
Vous êtes ici:
Support technique