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MMAA Protein (Myc-DYKDDDDK Tag)

MMAA Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2726115
  • Target Alle MMAA Proteine anzeigen
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 1
    Human
    Quelle
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses MMAA Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human MMAA protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MMAA Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Andere Bezeichnung
    Mmaa (MMAA Produkte)
    Synonyme
    2810018E08Rik Protein, AI840684 Protein, cblA Protein, methylmalonic aciduria (cobalamin deficiency) type A Protein, methylmalonic aciduria (cobalamin deficiency) cblA type Protein, Mmaa Protein, MMAA Protein
    Hintergrund
    The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.
    Molekulargewicht
    39 kDa
    NCBI Accession
    NP_758454
    Pathways
    Monocarboxylic Acid Catabolic Process
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