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Anti-FMO3 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Anti-FMO3 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
  BOSSBS-13186R-A750
 :  Bioss
Anti-FMO3 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
  BOSSBS-13186R-A750
 :  Bioss

 

  • Antibody type:
    Primary
  • Antigen name:
    FMO3
  • Clonality:
    Polyclonal
  • Conjugation:
    Alexa Fluor® 750
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Reactivity:
  • Western blot:
    Yes
  • Environmentally Preferable:
  • Epitope:
    111-210/532
  • Form:
    Liquid
  • Gene ID:
    2328
  • Antigen synonyms:
    FMO3_HUMAN|FMO II|Hepatic flavin containing monooxygenase 3|dJ127D3.1|FMO form 2|FMO 3|Dimethylaniline oxidase 3|Hepatic flavin-containing monooxygenase 3|FMOII|FMO3|Trimethylamine monooxygenase|Flavin containing monooxygenase 3|MGC34400|Dimethylaniline monooxygenase 3|Dimethylaniline monooxygenase [N oxide forming] 3|TMAU|Dimethylaniline monooxygenase [N-oxide-forming] 3
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol.
  • Molecular weight:
    60 kDa
  • Storage temperature:
    Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human FMO3
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

 

 

The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.

Type: Primary
Antigen: FMO3
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 111-210/532
Host: Rabbit
Isotype: IgG
Reactivity: