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MAOB (基因名), Amine oxidase [flavin-containing] B (蛋白名), aofb_human.
产品名称:

Human MAOB/ Amine oxidase [flavin-containing] B Recombinant Protein
氨氧化酶[含黄素]B

货号:

R9775h

商标:
EIAab®
监管等级:
别名:

Monoamine oxidase type B, MAO-B

序列号:
P27338
来源:
E.coli
种属:
Human
标签:
His
序列:
39-147aa
预估分子量:
11.99 kDa (monomer)
纯度:
Greater than 90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Neurosciences
Human MAOB Protein
规格 & 价格: cart
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human MAOB Protein
Recombinant human MAOB protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: Xp11.3 by HGNC Xp11.3 by Entrez Gene Xp11.3 by Ensembl
MAOB Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Monomer, homo- or heterodimer (containing two subunits of similar size). Each subunit contains a covalently bound flavin. Enzymatically active as monomer.


功能:
Catalyzes the oxidative deamination of biogenic and xenobiotic amines and has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAOB preferentially degrades benzylamine and phenylethylamine.


亚细胞位置:
Mitochondrion outer membrane Single-pass type IV membrane protein Cytoplasmic side


该产品尚未在任何出版物中被引用。

[1].
"A common variant in DRD3 gene is associated with risperidone-induced extrapyramidal symptoms."

[2].
"Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans."

[3].
"Association of A/G polymorphism in intron 13 of the monoamine oxidase B gene with schizophrenia in a Spanish population."

[4].
"Gene-gene interaction between FGF20 and MAOB in Parkinson disease."

[5].
"The monoamine oxidase B gene exhibits significant association to ADHD."

[6].
"Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder."

[7].
"Monoamine oxidase (MAO) intron 13 polymorphism and platelet MAO-B activity in combat-related posttraumatic stress disorder."

[8].
"Polymorphisms of catechol-0-methyltransferase (COMT), monoamine oxidase B (MAOB), N-acetyltransferase 2 (NAT2) and cytochrome P450 2D6 (CYP2D6) gene in patients with early onset of Parkinson's disease."

[9].
"Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue."

[10].
"Obesity is associated with genetic variants that alter dopamine availability."
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