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二甲基苯胺单加氧酶3抗体

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产物名称: 二甲基苯胺单加氧酶3抗体
产物型号: FMO3
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

二甲基苯胺单加氧酶3抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。二甲基苯胺单加氧酶3抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


二甲基苯胺单加氧酶3抗体  的详细介绍

二甲基苯胺单加氧酶3抗体

规格:1尘驳/1尘濒

英文名: FMO3

别名: Dimethylaniline monooxygenase [N oxide forming] 3; Dimethylaniline monooxygenase [N-oxide-forming] 3; Dimethylaniline monooxygenase 3; Dimethylaniline oxidase 3; dJ127D3.1; Flavin containing monooxyge

分子量: 60kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human FMO3

交叉反应:Human, Mouse, Rat, Cow, Monkey,

细胞定位:细胞浆 细胞膜

二甲基苯胺单加氧酶3抗体产物介绍:background: 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. Function: Involved in the oxidative metabolism of a variety 二甲基苯胺单加氧酶3抗体of xenobiotics such as drugs and pesticides. It N-oxygenates primary aliphatic alkylamines as well as secondary and tertiary amines. Plays an important role in the metabolism of trimethylamine (TMA), via the production of TMA N-oxide (TMAO). Is also able to perform S-oxidation when acting on sulfide compounds. Subcellular Location: Microsome membrane. Endoplasmic reticulum membrane. Tissue Specificity: Liver. Post-translational modifications: Belongs to the FMO family. DISEASE: Defects in FMO3 are the cause of trimethylaminuria (TMAU) [MIM:602079]; also known as fish-odor syndrome. TMAU is an inborn error of metabolism associated with an offensive body odor and caused by deficiency of FMO-mediated N-oxidation of amino-trimethylamine (TMA) derived from foodstuffs. Such individuals excrete relatively large amounts of TMA in their urine, sweat,二甲基苯胺单加氧酶3抗体 and breath, and exhibit a fishy body odor characteristic of the malodorous free amine. Similarity: Belongs to the FMO family. Database links: UniProtKB/Swiss-Prot: P31513.5 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

二甲基苯胺单加氧酶3抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  信号转导  新陈代谢  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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