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Choactase Rabbit pAb

-YT0909

2
主要信息
Target

Choactase

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, ELISA

MW

82,70kD (Observed)

Conjugate/Modification

Unmodified

货号: YT0909
规格
价格
货期
数量
200μL
¥3,780.00
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0

100μL
¥2,300.00
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40μL
¥960.00
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0

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详细信息
推荐稀释比
WB 1:500-1:2000; ELISA 1:10000; Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
Choactase Polyclonal Antibody detects endogenous levels of Choactase 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
82,70kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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抗原&靶点信息
免疫原:
The antiserum was produced against synthesized peptide derived from human Choactase. AA range:334-383
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特异性:
Choactase Polyclonal Antibody detects endogenous levels of Choactase protein.
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基因名称:
CHAT
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蛋白名称:
Choline O-acetyltransferase
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别名:
CHAT ;
Choline O-acetyltransferase ;
CHOACTase ;
ChAT ;
Choline acetylase
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数据库链接:
Organism 基因 ID SwissProt
Human 1103; P28329;
Mouse Q03059;
Rat P32738;
背景:
This gene encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform. [provided by RefSeq, May 2010],
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功能:
Catalytic activity:Acetyl-CoA + choline = CoA + O-acetylcholine.,Disease:Defects in CHAT are the cause of congenital myasthenic syndrome with episodic apnea (CMSEA) [MIM:254210]; formerly known as familial infantile myasthenia gravis 2 (FIMG2). CMSEA is an autosomal recessive congenital myasthenic syndrome. Patients have myasthenic symptoms since birth or early infancy, negative tests for anti-AChR antibodies, and abrupt episodic crises with increased weakness, bulbar paralysis, and apnea precipitated by undue exertion, fever, or excitement.,Function:Catalyzes the reversible synthesis of acetylcholine (ACh) from acetyl CoA and choline at cholinergic synapses.,online information:Choline acetyltransferase entry,similarity:Belongs to the carnitine/choline acetyltransferase family.,
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细胞定位:
nucleus,cytoplasm,cytosol,presynapse,
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组织表达:
Brain,Lymphocyte,Placenta,Spinal cord,
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研究领域:
>>Glycerophospholipid metabolism ;
>>Cholinergic synapse
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货号: YT0909
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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