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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY0653

Tyrosine Hydroxylase Rabbit mAb

Tyrosine 3-monooxygenase;Tyrosine 3-hydroxylase;TH;

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别名 Tyrosine 3-monooxygenase;Tyrosine 3-hydroxylase;TH;
基因名称 Tyrosine Hydroxylase
蛋白名称 Tyrosine 3-monooxygenase (Tyrosine 3-hydroxylase) (TH),Tyrosine Hydrolase
推荐应用
反应物种 Human,Mouse,Rat
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link 7054
Human Swissprot No. P07101
Mouse Gene ID 21823
Mouse Swissprot No. P24529
Rat Gene ID 25085
Rat Swissprot No. P04177
特异性 endogenous
稀释度 IHC 1:500-1:2000;WB 1:1000-1:5000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
参考分子量 MW(Observed):59kD
预测分子量 MW(Calculated):59kD
运输及保存条件 -15°C to -25°C/1 year(Do not lower than -25°C)
宿主 Rabbit
同种型 IgG,Kappa
背景介绍 The protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008],
细胞定位 Cytoplasm. Nucleus.
功能 Catalytic activity:L-tyrosine + tetrahydrobiopterin + O(2) = 3,4-dihydroxy-L-phenylalanine + 4a-hydroxytetrahydrobiopterin.,cofactor:Fe(2+) ion.,Disease:Defects in TH are the cause of dystonia DOPA-responsive autosomal recessive (ARDRD) [MIM:605407]; also known as autosomal recessive Segawa syndrome. ARDRD is a form of DOPA-responsive dystonia presenting in infancy or early childhood. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Some cases of ARDRD present with parkinsonian symptoms in infancy. Unlike all other forms of dystonia, it is an eminently treatable condition, due to a favorable response to L-DOPA.,enzyme regulation:Phosphorylation leads to an increase in the catalytic activity.,Function:Plays an important role in the physiology of adrenergic neurons.,online information:Tyrosine hydroxylase entry,pathway:Catecholamine biosynthesis; dopamine biosynthesis; dopamine from L-tyrosine: step 1/2.,similarity:Belongs to the biopterin-dependent aromatic amino acid hydroxylase family.,tissue specificity:Mainly expressed in the brain and adrenal glands.,
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Cytoplasm. Nucleus.
组织表达 Mainly expressed in the brain and adrenal glands.
研究领域 >>Tyrosine metabolism;>>Folate biosynthesis;>>Metabolic pathways;>>Dopaminergic synapse;>>Prolactin signaling pathway;>>Parkinson disease;>>Cocaine addiction;>>Amphetamine addiction;>>Alcoholism

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