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MMAA Protein (Myc-DYKDDDDK Tag)

MMAA Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2726115
  • Target See all MMAA Proteins
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Protein Type
    Recombinant
    Origin
    • 3
    • 1
    • 1
    Human
    Source
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This MMAA protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human MMAA protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MMAA Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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))
    Alternative Name
    Mmaa (MMAA Products)
    Synonyms
    2810018E08Rik Protein, AI840684 Protein, cblA Protein, methylmalonic aciduria (cobalamin deficiency) type A Protein, methylmalonic aciduria (cobalamin deficiency) cblA type Protein, Mmaa Protein, MMAA Protein
    Background
    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.
    Molecular Weight
    39 kDa
    NCBI Accession
    NP_758454
    Pathways
    Monocarboxylic Acid Catabolic Process
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