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MMAB antibody

MMAB Reactivity: Human WB, IHC, FACS Host: Mouse Monoclonal 5G1 unconjugated
Catalog No. ABIN2726120
  • Target See all MMAB Antibodies
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Reactivity
    • 8
    • 3
    Human
    Host
    • 5
    • 3
    Mouse
    Clonality
    • 6
    • 2
    Monoclonal
    Conjugate
    • 8
    This MMAB antibody is un-conjugated
    Application
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
    Characteristics
    Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB), nuclear gene encoding mitochondrial protein, transcript variant 1
    Purification
    Purified from mouse ascites fluids by affinity chromatography
    Immunogen
    Full length human recombinant protein of human MMAB (NP_443077) produced in HEK293T cell.
    Clone
    5G1
    Isotype
    IgG2a
    Top Product
    Discover our top product MMAB Primary Antibody
  • Application Notes
    WB 1:500, IHC 1:150, FLOW 1:100
    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5-1.0 mg/mL
    Buffer
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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
    -20 °C
  • Target
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Alternative Name
    MMAB (MMAB Products)
    Synonyms
    ATR antibody, cblB antibody, cob antibody, 9130222L19Rik antibody, methylmalonic aciduria (cobalamin deficiency) cblB type antibody, methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) antibody, MMAB antibody, Mmab antibody
    Background
    This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group.
    Molecular Weight
    24.0 kDa
    Gene ID
    326625
    NCBI Accession
    NM_052845
    HGNC
    326625
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