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MAO-A Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT2635
产品名称
MAO-A Rabbit Polyclonal Antibody
别名
MAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A
类别
常规抗体
基因名称
MAOA
蛋白名称
Amine oxidase [flavin-containing] A
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
4128
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4128
Human Swissprot No.
P21397
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P21397/entry
Mouse Gene ID
17161
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=17161
Mouse Swissprot No.
Q64133
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q64133
Rat Swissprot No.
P21396
Rat Swissprot Link
http://www.uniprot.org/uniprot/P21396
免疫原
The antiserum was produced against synthesized peptide derived from human MAO-A. AA range:298-347
特异性
MAO-A Polyclonal Antibody detects endogenous levels of MAO-A protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:20000.. IF 1:50-200
预测分子量
61kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012],
组织表达
Heart, liver, duodenum, blood vessels and kidney.
细胞定位
Mitochondrion outer membrane ; Single-pass type IV membrane protein ; Cytoplasmic side .
信号通路
Glycine; serine and threonine metabolism;Arginine and proline metabolism;Histidine metabolism;Tyrosine metabolism;Phenylalanine metabolism;Tryptophan metabolism;Drug metabolism;
功能
catalytic activity:RCH(2)NHR' + H(2)O + O(2) = RCHO + R'NH(2) + H(2)O(2).,cofactor:FAD.,disease:Defects in MAOA are the cause of Brunner syndrome (BRUNS) [MIM:300615]. Brunner syndrome is a form of X-linked non-dysmorphic mild mental retardation. Male patients are affected by a syndrome of borderline mental retardation and exhibit abnormal behavior, including disturbed regulation of impulsive aggression. Obligate female carriers have normal intelligence and behavior.,function: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. MAOA preferentially oxidizes biogenic amines such as 5-hydroxytryptamine (5-HT), norepinephrine and epinephrine.,mass spectrometry: PubMed:11812236,online information:Monoamine oxidase entry,similarity:Belongs to the flavin monoamine oxidase family.,subunit:Monomer, homo- or heterodimer (containing two subunits of similar size). Each subunit contains a covalently bound flavin. Enzymatically active as monomer.,tissue specificity:Heart, liver, duodenum, blood vessels and kidney.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunohistochemistry analysis of MAO-A antibody in paraffin-embedded human brain tissue.

Western blot analysis of lysate from HeLa cells, using MAO-A antibody.

Western Blot analysis of various cells using MAO-A Polyclonal Antibody diluted at 1:1000

Western Blot analysis of HeLa cells using MAO-A Polyclonal Antibody diluted at 1:1000

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