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MCEE Protein (His tag)

MCEE Origine: Humain Hôte: Human Cells Recombinant > 95 % as determined by reducing SDS-PAGE.
N° du produit ABIN7318778
  • Antigène Voir toutes MCEE Protéines
    MCEE (Methylmalonyl CoA Epimerase (MCEE))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 2
    • 2
    • 1
    Humain
    Source
    • 5
    • 1
    • 1
    • 1
    Human Cells
    Purification/Conjugué
    Cette MCEE protéine est marqué à la His tag.
    Fonction
    Recombinant Human MCEE Protein (His Tag)
    Séquence
    Gln37-Ala176
    Attributs du produit
    Recombinant Human Methylmalonyl-CoA epimerase is produced by our Mammalian expression system and the target gene encoding Gln37-Ala176 is expressed with a 6His tag at the C-terminus.
    Pureté
    > 95 % as determined by reducing SDS-PAGE.
    niveau d'endotoxine
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product MCEE Protéine
  • Restrictions
    For Research Use only
  • Format
    Frozen, Liquid
    Buffer
    Supplied as a 0.2 μm filtered solution of 20 mM TrisHCl,150 mM NaCl,1 mM DTT,10 % Glycerol, pH 7.5.
    Stock
    -20 °C
    Stockage commentaire
    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Antigène
    MCEE (Methylmalonyl CoA Epimerase (MCEE))
    Autre désignation
    MCEE (MCEE Produits)
    Synonymes
    MGC89112 Protein, zgc:112343 Protein, MGC116480 Protein, GLOD2 Protein, 1110007A04Rik Protein, methylmalonyl-CoA epimerase Protein, methylmalonyl CoA epimerase Protein, methylmalonyl-CoA epimerase S homeolog Protein, MCEE Protein, mcee Protein, mcee.S Protein, Mcee Protein
    Sujet

    Background: Methylmalonyl-CoA epimerase, mitochondrial(MCEE)is an enzyme which belongs to the glyoxalase I family. It converts (S)-methylmalonyl-CoA to the (R) form, catalyses the following chemical reaction: (R)-methylmalonyl-CoA (S)-methylmalonyl-CoA. It plays an important role in the catabolism of fatty acids with odd-length carbon chains. This protein deficiency is an autosomal recessive inborn error of AA metabolism, involving valine, threonine, isoleucine and methionine. This organic aciduria can appear in the neonatal period with life-threatening metabolic acidosis, hyperammonemia, feeding difficulties, pancytopenia and coma.

    Synonym: Methylmalonyl-CoA epimerase, mitochondrial,DL-methylmalonyl-CoA racemase

    Poids moléculaire
    16.0 kDa
    UniProt
    Q96PE7
    Pathways
    Monocarboxylic Acid Catabolic Process
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