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ACHA2 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN3716
产品名称
ACHA2 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
CHRNA2
蛋白名称
ACHA2
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
1135
Human Gene Link
https://www.uniprot.org/uniprot/1135
Human Swissprot No.
Q15822
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q15822/entry
Mouse Gene ID
110902
Mouse Gene Link
https://www.uniprot.org/uniprot/110902
Mouse Swissprot No.
Q91X60
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q91X60
Rat Gene ID
170945
Rat Gene Link
https://www.uniprot.org/uniprot/170945
Rat Swissprot No.
P12389
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/P12389
免疫原
Synthesized peptide derived from human ACHA2 AA range: 219-269
特异性
This antibody detects endogenous levels of ACHA2 at Human/Mouse/Rat
稀释度
WB 1:500-2000
参考分子量
58kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels formed by a pentameric arrangement of alpha and beta subunits to create distinct muscle and neuronal receptors. Neuronal receptors are found throughout the peripheral and central nervous system where they are involved in fast synaptic transmission. This gene encodes an alpha subunit that is widely expressed in the brain. The proposed structure for nAChR subunits is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4. Single nucleotide polymorphisms (SNPs) in this gene have been associated with nicotine dependence. [provided by RefSeq, Nov 2009],
细胞定位
Cell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein.
功能
disease:Defects in CHRNA2 are the cause of nocturnal frontal lobe epilepsy type 4 (ENFL4) [MIM:610353]. ENFL4 is an autosomal dominant epilepsy characterized by nocturnal seizures associated with fear sensation, tongue movements, and nocturnal wandering, closely resembling nightmares and sleep walking.,function: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.,similarity:Belongs to the ligand-gated ionic channel (TC 1.A.9) family.,subunit:Neuronal AChR seems to be composed of two different types of subunits: alpha and non-alpha (beta). Alpha-2 subunit can be combined to beta-2 or beta-4 to give rise to functional receptors.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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