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Tyrosine Hydroxylase Rabbit pAb

-YT4640

2 5
主要信息
Target

Tyrosine Hydroxylase

Host Species

Rabbit

Reactivity

Human, Mouse, Rat, Monkey

Applications

WB, IHC, IF, ELISA

MW

60kD (Observed)

Conjugate/Modification

Unmodified

货号: YT4640
规格
价格
货期
数量
200μL
¥3,780.00
一个月

0

100μL
¥2,300.00
一个月

0

40μL
¥960.00
一个月

0

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详细信息
推荐稀释比
WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:20000; IF 1:50-200
Note:For IHC,wesuggest antigen retrieval with TE buffer pH 9.0 (Cat#YS0004)
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
TH Polyclonal Antibody detects endogenous levels of TH protein.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
实测条带
60kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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ELISA Kits
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ELISA Kits
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抗原&靶点信息
免疫原:
The antiserum was produced against synthesized peptide derived from human Tyrosine Hydroxylase. AA range:1-50
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特异性:
TH Polyclonal Antibody detects endogenous levels of TH protein.
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基因名称:
TH
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蛋白名称:
Tyrosine 3-monooxygenase (Tyrosine 3-hydroxylase) (TH),Tyrosine Hydrolase
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别名:
TH ;
TYH ;
Tyrosine 3-monooxygenase ;
Tyrosine 3-hydroxylase ;
TH
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数据库链接:
Organism 基因 ID SwissProt
Human 7054; P07101;
Mouse 21823; P24529;
Rat 25085; P04177;
背景:
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],
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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.,
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细胞定位:
Cytoplasm, perinuclear region . Nucleus . Cell projection, axon . Cytoplasm . Cytoplasmic vesicle, secretory vesicle, synaptic vesicle . When phosphorylated at Ser-19 shows a nuclear distribution and when phosphorylated at Ser-31 as well at Ser-40 shows a cytosolic distribution (By similarity). Expressed in dopaminergic axons and axon terminals. .
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组织表达:
Mainly expressed in the brain and adrenal glands.
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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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货号: YT4640
规格
价格
货期
数量
200μL
¥3,780.00
一个月

0

100μL
¥2,300.00
一个月

0

40μL
¥960.00
一个月

0

加入购物车

已收藏

收藏

定制服务咨询

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