Anti-FMO3 antibody
英文名称 | FMO3 |
中文名称 | 二甲基苯胺单加氧酶3抗体 |
别 名 | Dimethylaniline monooJNCgenase [N oxide forming] 3; Dimethylaniline monooJNCgenase [N-oxide-forming] 3; Dimethylaniline monooJNCgenase 3; Dimethylaniline oxidase 3; dJ127D3.1; Flavin containing monooJNCgenase 3; FMO 3; FMO form 2; FMO II; FMO3; FMO3_HUMAN; FMOII; Hepatic flavin containing monooJNCgenase 3; Hepatic flavin-containing monooJNCgenase 3; MGC34400; TMAU; Trimethylamine monooJNCgenase. |
DATASHEET
Host:Rabbit
Target Protein:FMO3
IR:Immunogen Range:111-210/532
Clonality:Polyclonal
Isotype:IgG
Entrez Gene:2328
Swiss Prot:P31513
Source:KLH conjugated synthetic peptide derived from human FMO3:111-210/532
Purification:affinity purified by Protein A
Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Background:The Flavin containing monooJNCgenase 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 oJNCgenates soft nucleophiles such as secondary and tertiary amines. Through its N-oJNCgenase 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.
Size:100ul
Concentration:1mg/ml
Applications:WB(1:500-2000)
ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
ICC(1:100-500)
IF(1:100-500)
Cross Reactive Species:Human
Mouse
Rat
Cow
Monkey
.
For research use only. Not intended for diagnostic or therapeutic use.
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