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FMO2 anticorps

FMO2 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN4951058
  • Antigène Voir toutes FMO2 Anticorps
    FMO2 (Flavin Containing Monooxygenase 2 (Non-Functional) (FMO2))
    Reactivité
    • 11
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain
    Hôte
    • 12
    Lapin
    Clonalité
    • 12
    Polyclonal
    Conjugué
    • 12
    Cet anticorp FMO2 est non-conjugé
    Application
    • 11
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity
    Immunogène
    Amino acids FPNFLHNSKLLEYFRIFAKKFDLLKYIQFQTTVLSVRK of human FMO2 were used as the immunogen for the FMO2 antibody.
    Isotype
    IgG
    Top Product
    Discover our top product FMO2 Anticorps primaire
  • Indications d'application
    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
    Stock
    -20 °C
    Stockage commentaire
    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.
  • Antigène
    FMO2 (Flavin Containing Monooxygenase 2 (Non-Functional) (FMO2))
    Autre désignation
    FMO2 (FMO2 Produits)
    Synonymes
    anticorps FMO 1B1, anticorps FMO 2, anticorps FMO1B1, anticorps 2310008D08Rik, anticorps 2310042I22Rik, anticorps AW107733, anticorps MGC68715, anticorps FMO4, anticorps FMO2, anticorps flavin containing monooxygenase 2, anticorps flavin containing monooxygenase 2 L homeolog, anticorps FMO2, anticorps Fmo2, anticorps fmo2.L
    Sujet
    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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