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MMAA antibody (N-Term)

MMAA Reactivity: Human, Mouse WB, IHC (p) Host: Rabbit Polyclonal RB24782 unconjugated
Catalog No. ABIN653752
  • Target See all MMAA Antibodies
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Binding Specificity
    • 9
    • 7
    • 4
    • 2
    • 1
    AA 56-84, N-Term
    Reactivity
    • 33
    • 22
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 30
    • 3
    Rabbit
    Clonality
    • 32
    • 1
    Polyclonal
    Conjugate
    • 9
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MMAA antibody is un-conjugated
    Application
    • 33
    • 14
    • 13
    • 12
    • 5
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.
    Clone
    RB24782
    Isotype
    Ig Fraction
  • Application Notes
    WB: 1:500. WB: 1:1000. IHC-P: 1:50~100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Alternative Name
    MMAA (MMAA Products)
    Synonyms
    2810018E08Rik antibody, AI840684 antibody, cblA antibody, methylmalonic aciduria (cobalamin deficiency) type A antibody, methylmalonic aciduria (cobalamin deficiency) cblA type antibody, Mmaa antibody, MMAA antibody
    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
    46538
    Gene ID
    166785
    NCBI Accession
    NP_758454
    UniProt
    Q8IVH4
    Pathways
    Monocarboxylic Acid Catabolic Process
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