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MCEE Protein (AA 37-176) (His tag)

MCEE Spezies: Human Wirt: HEK-293 Cells Recombinant >95 % as determined by reducing SDS-PAGE.
Produktnummer ABIN7505580
  • Target Alle MCEE Proteine anzeigen
    MCEE (Methylmalonyl CoA Epimerase (MCEE))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    AA 37-176
    Spezies
    • 3
    • 2
    • 2
    • 1
    Human
    Quelle
    • 5
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses MCEE Protein ist gelabelt mit His tag.
    Sequenz
    Gln37-Ala176
    Produktmerkmale
    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.
    Reinheit
    >95 % as determined by reducing SDS-PAGE.
    Endotoxin-Niveau
    <1.0 EU per μg of the protein as determined by the LAL method.
    Top Product
    Discover our top product MCEE Protein
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Buffer
    Lyophilized from sterile PBS, pH 7.4., 5 % trehalose, 5 % mannitol, 0.01 % tween-80.
    Lagerung
    4 °C,-20 °C,-80 °C
    Informationen zur Lagerung
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
    Haltbarkeit
    12 months
  • Target
    MCEE (Methylmalonyl CoA Epimerase (MCEE))
    Andere Bezeichnung
    MCEE (MCEE Produkte)
    Synonyme
    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
    Hintergrund

    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

    Molekulargewicht
    16.0 kDa
    UniProt
    Q96PE7
    Pathways
    Monocarboxylic Acid Catabolic Process
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