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α-Conotoxin BuIA 是一种麻痹性肽类神经毒素,同时也是竞争性nAChR拮抗剂。它对nAChR亚型表现出不同的IC50值:0.258 nM(α6/α3β2)、1.54 nM(α6/α3β4)、5.72 nM(α3β2)。该化合物可用于鉴别包含β2与β4亚单位的nAChR亚型。此外,α-Conotoxin BuIA 对αxβ2nAChR的区分能力按照α6>α3>α2>α4的顺序减弱。

α-Conotoxin BuIA 是一种麻痹性肽类神经毒素,同时也是竞争性nAChR拮抗剂。它对nAChR亚型表现出不同的IC50值:0.258 nM(α6/α3β2)、1.54 nM(α6/α3β4)、5.72 nM(α3β2)。该化合物可用于鉴别包含β2与β4亚单位的nAChR亚型。此外,α-Conotoxin BuIA 对αxβ2nAChR的区分能力按照α6>α3>α2>α4的顺序减弱。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
α-Conotoxin BuIA 相关产品
| 产品描述 | α-Conotoxin BuIA is a paralytic peptide neurotoxin that acts as a competitive antagonist of nicotinic acetylcholine receptors (nAChR), with inhibitory concentration 50 (IC50) values of 0.258 nM for α6/α3β2, 1.54 nM for α6/α3β4, and 5.72 nM for α3β2. It serves to differentiate between nAChRs containing the β2- and β4-subunits. Furthermore, α-Conotoxin BuIA selectively inhibits αxβ2 nAChRs, exhibiting a potency hierarchy of α6>α3>α2>α4 [1]. |
| 分子量 | 1311.57 |
| 分子式 | C54H82N14O16S4 |
| CAS No. | 846539-62-6 |
| Sequence | Gly-Cys-Cys-Ser-Thr-Pro-Pro-Cys-Ala-Val-Leu-Tyr-Cys-NH2 (Disulfide bridge: Cys2-Cys8, Cys3-Cys13) |
| Sequence Short | GCCSTPPCAVLYC-NH2 (Disulfide bridge: Cys2-Cys8, Cys3-Cys13) |
| 存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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