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MLYCD Protein (Myc-DYKDDDDK Tag)

MLYCD Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2726112
  • Antigène Voir toutes MLYCD Protéines
    MLYCD (Malonyl CoA Decarboxylase (MLYCD))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 2
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette MLYCD protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human MLYCD 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 MLYCD 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
    MLYCD (Malonyl CoA Decarboxylase (MLYCD))
    Autre désignation
    Mlycd (MLYCD Produits)
    Synonymes
    MCD Protein, AI324784 Protein, Mcd Protein, MaLonyl CoA Decarboxylase Protein, malonyl-CoA decarboxylase Protein, mlcd-1 Protein, MLYCD Protein, Mlycd Protein
    Sujet
    The product of this gene catalyzes the breakdown of malonyl-CoA to acetyl-CoA and carbon dioxide. Malonyl-CoA is an intermediate in fatty acid biosynthesis, and also inhibits the transport of fatty acyl CoAs into mitochondria. Consequently, the encoded protein acts to increase the rate of fatty acid oxidation. It is found in mitochondria, peroxisomes, and the cytoplasm. Mutations in this gene result in malonyl-CoA decarboyxlase deficiency.
    Poids moléculaire
    54.8 kDa
    NCBI Accession
    NP_036345
    Pathways
    Regulation of Carbohydrate Metabolic Process
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