|Application ||WB, E|
|Calculated MW||60221 Da|
|Antigen Region||474-502 aa|
|Other Names||Dimethylaniline monooxygenase [N-oxide-forming] 5, Dimethylaniline oxidase 5, Hepatic flavin-containing monooxygenase 5, FMO 5, FMO5|
|Target/Specificity||This FMO5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 474-502 amino acids from the C-terminal region of human FMO5.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||FMO5 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||In contrast with other forms of FMO it does not seem to be a drug-metabolizing enzyme.|
|Cellular Location||Microsome membrane. Endoplasmic reticulum membrane|
|Tissue Location||Expressed in fetal and adult liver.|
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abgent to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Metabolic N-oxidation of the diet-derived amino-trimethylamine (TMA) is mediated by flavin-containing monooxygenase and is subject to an inherited FMO3 polymorphism in man resulting in a small subpopulation with reduced TMA N-oxidation capacity resulting in fish odor syndrome Trimethylaminuria. Three forms of the enzyme, FMO1 found in fetal liver, FMO2 found in adult liver, and FMO3 are encoded by genes clustered in the 1q23-q25 region. Flavin-containing monooxygenases are NADPH-dependent flavoenzymes that catalyzes the oxidation of soft nucleophilic heteroatom centers in drugs, pesticides, and xenobiotics. Alternative splicing results in multiple transcript variants.
Rose, J. Phd, et al. Mol. Med. (2010) In press :
Ross, C.J., et al. Nat. Genet. 41(12):1345-1349(2009)
Wheeler, H.E., et al. PLoS Genet. 5 (10), E1000685 (2009) :
Zhang, J., et al. Drug Metab. Dispos. 34(1):19-26(2006)
Furnes, B., et al. Drug Metab. Dispos. 31(2):187-193(2003)
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