本公司所有产品仅供科研使用,不用于人体及临床诊断。
027-59234612(+86)
我的积分
注册  /  登录
EIAab
首页  >  酶联免疫试剂盒  >  Mouse Chrne ELISA Kit
Chrne (基因名), Acetylcholine receptor subunit epsilon (蛋白名), ACHE_MOUSE.
产品名称:

Mouse Chrne/ Acetylcholine receptor subunit epsilon ELISA Kit

货号:
-
商标:
EIAab®
监管等级:
别名:

Acre

检测方法:
ELISA
特异性:
Natural and recombinant mouse Acetylcholine receptor subunit epsilon
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
Neurosciences
Mouse Chrne ELISA Kit
规格 & 价格: 登录.
×
Mouse Chrne ELISA Kit
邮箱 *
消息 *
Please 登录.
产品说明书


通用注释


亚单元:
Pentamer of two alpha chains, and one each of the beta, delta, and gamma (in immature muscle) or epsilon (in mature muscle) chains.


功能:
After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane.


亚细胞位置:
Cell junction Synapse Postsynaptic cell membrane Multi-pass membrane protein Cell membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Primary structure of the human muscle acetylcholine receptor. cDNA cloning of the gamma and epsilon subunits."

[2].
"Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel Gating."

[3].
"A large-scale candidate gene association study of age at menarche and age at natural menopause."

[4].
"Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment."

[5].
"Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes."

[6].
"The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa."

[7].
"Lack of association between acetylcholine receptor epsilon polymorphisms and early-onset myasthenia gravis."

[8].
"Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome."

[9].
"Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by epsilon-AChR subunit truncating mutations."

[10].
"Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations."
关闭
Sample Data
关闭
Sample Data
关闭
Sample Data
用户中心 close
购物车 close
我的收藏 close
我的足迹 close
清除
产品对比 close
用户中心
购物车
我的收藏
我的足迹
产品对比
回到顶部
消息
close_message
产品名称 *
邮箱 *
消息 *
通知
new 留 言
规格 数量 价格 ($) 小计 1 ($)
小计 2: $
triangle
规格 数量 价格 ($)
你想做我们的代理并得到更低的折扣吗?
请联系我们:
电话:027-59234612(+86)
传真:027-59759960(+86)
邮箱:sales@eiaab.com