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首页  >  重组蛋白  >  Human CHRND Recombinant Protein
CHRND (基因名), Acetylcholine receptor subunit delta (蛋白名), ACHD_HUMAN.
产品名称:

Human CHRND/ Acetylcholine receptor subunit delta Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

ACHRD

序列号:
Q07001
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Neurosciences
Human CHRND Protein
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Human CHRND Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 2q37.1 by HGNC 2q37.1 by Entrez Gene 2q37.1 by Ensembl
CHRND Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
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].
"Association of the gene encoding the delta-subunit of the muscle acetylcholine receptor (CHRND) with acquired autoimmune myasthenia gravis."

[2].
"Human variation in alcohol response is influenced by variation in neuronal signaling genes."

[3].
"Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans."

[4].
"A large-scale candidate gene association study of age at menarche and age at natural menopause."

[5].
"Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis."

[6].
"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."

[7].
"Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes."

[8].
"Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders."

[9].
"Congenital myasthenia-related AChR delta subunit mutation interferes with intersubunit communication essential for channel gating."

[10].
"Nicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study."
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