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FMO2 antibody

FMO2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN4951058
  • Target See all FMO2 Antibodies
    FMO2 (Flavin Containing Monooxygenase 2 (Non-Functional) (FMO2))
    Reactivity
    • 11
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Host
    • 12
    Rabbit
    Clonality
    • 12
    Polyclonal
    Conjugate
    • 12
    This FMO2 antibody is un-conjugated
    Application
    • 11
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity
    Immunogen
    Amino acids FPNFLHNSKLLEYFRIFAKKFDLLKYIQFQTTVLSVRK of human FMO2 were used as the immunogen for the FMO2 antibody.
    Isotype
    IgG
    Top Product
    Discover our top product FMO2 Primary Antibody
  • Application Notes
    Optimal dilution of the FMO2 antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the FMO2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    FMO2 (Flavin Containing Monooxygenase 2 (Non-Functional) (FMO2))
    Alternative Name
    FMO2 (FMO2 Products)
    Synonyms
    FMO 1B1 antibody, FMO 2 antibody, FMO1B1 antibody, 2310008D08Rik antibody, 2310042I22Rik antibody, AW107733 antibody, MGC68715 antibody, FMO4 antibody, FMO2 antibody, flavin containing monooxygenase 2 antibody, flavin containing monooxygenase 2 L homeolog antibody, FMO2 antibody, Fmo2 antibody, fmo2.L antibody
    Background
    Dimethylaniline monooxygenase [N-oxide-forming] 2 is an enzyme that in humans is encoded by the FMO2 gene (flavin containing monooxygenase 2). It is an NADPH-dependent enzyme that catalyzes the N-oxidation of some primary alkylamines through an N-hydroxylamine intermediate. However, some human populations contain an allele (FMO2*2A) with a premature stop codon, resulting in a protein that is C-terminally-truncated, has no catalytic activity, and is likely degraded rapidly. This gene is found in a cluster with other related family members on chromosome 1. Alternative splicing results in multiple transcript variants.
    UniProt
    Q99518
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