当前位置:首页>产品中心>单抗/多抗>Anti-Human CHRNA7 Recombinant Nanobody |抗人CHRNA7纳米抗体(靶标:人烟碱型乙酰胆碱受体α7亚基)

Anti-Human CHRNA7 Recombinant Nanobody |抗人CHRNA7纳米抗体(靶标:人烟碱型乙酰胆碱受体α7亚基)

  • 货号:RB9THW806013
  • 价格:面议
  • 点击:642
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产品介绍

产品参数

形态Liquid
宿主种属Alpaca
克隆性Monoclonal
抗体亚型VHH-His
纯度>95% as determined by SDS-PAGE.
纯化方式Protein A/G purified from cell culture supernatant.
内毒素水平Please contact with the lab for this information.
应用ELISA
种属反应性Homo sapiens (Human)
靶标CHRNA7, NACHRA7, Neuronal acetylcholine receptor subunit alpha-7, Nicotinic acetylcholine receptor subunit alpha-7, nAChR7
储存缓冲液0.01M PBS pH 7.4
稳定性和储存Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
重构方法Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
登录号P36544
背景信息

Neuronal acetylcholine receptor subunit alpha-7 (CHRNA7) is a ~56 kDa protein. Component of neuronal acetylcholine receptors (nAChRs) that function as pentameric, ligand-gated cation channels with high calcium permeability among other activities. nAChRs are excitatory neurotrasnmitter receptors formed by a collection of nAChR subunits known to mediate synaptic transmission in the nervous system and the neuromuscular junction. Each nAchR subunit confers differential attributes to channel properties, including activation, deactivation and desensitization kinetics, pH sensitivity, cation permeability, and binding to allosteric modulators. CHRNA7 forms homopentameric neuronal acetylcholine receptors abundantly expressed in the central nervous system, characterized by fast desensitization and high calcium permeability. Also forms heteropentamers with CHRNB2, mainly expressed in basal forebrain cholinergic neurons.

1. Ellison, M. et al. (2004) Biochemistry 43, 16019-26. PMID: 15609996
2. Noviello, CM. et al. (2021) Cell 184, 2121-2134.e13. PMID: 33735609
3. Peng, X. et al. (1994) Molecular pharmacology 45, 546-54. PMID: 8145738
4. Nielsen, BE. et al. (2019) Neuropharmacology 160, 107794. PMID: 31560909
5. Burke, SM. et al. (2024) Cell 187, 1160-1176.e21. PMID: 38382524
6. George, AA. et al. (2021) The Journal of neuroscience : the official journal of the Society for Neuroscience 41, 555-575. PMID: 33239400
7. Wang, H. et al. (2003) Nature 421, 384-8. PMID: 12508119
8. Yoshikawa, H. et al. (2006) Clinical and experimental immunology 146, 116-23. PMID: 16968406
备注For research use only
【仅供科学研究使用】

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