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MMAB antibody (Middle Region)

MMAB Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5517725
  • Target See all MMAB Antibodies
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Binding Specificity
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivity
    • 8
    • 3
    Human
    Host
    • 5
    • 3
    Rabbit
    Clonality
    • 6
    • 2
    Polyclonal
    Conjugate
    • 8
    This MMAB antibody is un-conjugated
    Application
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    PRIPKIYTKT GDKGFSSTFT GERRPKDDQV FEAVGTTDEL SSAIGFALEL
    Purification
    Affinity purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the middle region of human MMAB
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    Discover our top product MMAB Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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. Alternatively spliced transcript variants have been found.

    Alias Symbols: ATR, cob, cblB, CFAP23

    Protein Size: 173
    Gene ID
    326625
    NCBI Accession
    NP_443077
    UniProt
    F5H4Z7
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