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BDS-I,又名降血物质,源自苏卡达银莲花的海洋毒素。它作为钾通道特异性抑制剂,针对Kv3.4。BDS-I能够抑制由Aβ1-42诱导的Kv3.4活性增强,减少caspase-3的激活,阻止NGF诱导的PC-12细胞分化以及异常核形态的出现,并可逆转Aβ肽引发的细胞死亡。
BDS-I,又名降血物质,源自苏卡达银莲花的海洋毒素。它作为钾通道特异性抑制剂,针对Kv3.4。BDS-I能够抑制由Aβ1-42诱导的Kv3.4活性增强,减少caspase-3的激活,阻止NGF诱导的PC-12细胞分化以及异常核形态的出现,并可逆转Aβ肽引发的细胞死亡。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
BDS-I 相关产品
| 产品描述 | BDS-I, a marine toxin derived from Anemonia sulcata, functions as a selective inhibitor of the potassium channel, specifically targeting Kv3.4. It impedes the Aβ1-42-induced augmentation of Kv3.4 activity, caspase-3 activation, and distortion of nuclear morphology in NGF-differentiated PC-12 cells. Moreover, BDS-I effectively counteracts the cell death induced by the Aβ peptide [1]. |
| 分子量 | 4708.34 |
| 分子式 | C210H297N57O56S6 |
| CAS No. | 207621-38-3 |
| Sequence | Ala-Ala-Pro-Cys-Phe-Cys-Ser-Gly-Lys-Pro-Gly-Arg-Gly-Asp-Leu-Trp-Ile-Leu-Arg-Gly-Thr-Cys-Pro-Gly-Gly-Tyr-Gly-Tyr-Thr-Ser-Asn-Cys-Tyr-Lys-Trp-Pro-Asn-Ile-Cys-Cys-Tyr-Pro-His (Disulfide bonds:Cys4-Cys39, Cys6-Cys32, Cys22-Cys40) |
| Sequence Short | AAPCFCSGKPGRGDLWILRGTCPGGYGYTSNCYKWPNICCYPH (Disulfide bonds:Cys4-Cys39, Cys6-Cys32, Cys22-Cys40) |
| 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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