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| 产品编号 | bs-42191P |
| 英文名称 | Recombinant human KCNT1 protein, N-Trx-His |
| 中文名称 | 重组人钾离子通道亚家族T成员1 |
| 别 名 | bA100C15.2; EIEE14; ENFL5; KCa4.1; KCNT1; KCNT1_HUMAN; Potassium channel subfamily T member 1; Potassium channel, subfamily T, member 1; SLACK. |
| 理论分子量 | 36.1kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | >2mg/ml |
| 物 种 | Human |
| 序 列 | 611-780/1230 |
| 纯 度 | >90% as determined by SDS-PAGE |
| 内毒素 | Not analyzed |
| 标签 | N-Trx-His |
| 缓 冲 液 | 20mM Tris-Hcl (pH=8.0) |
| 保存条件 | Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 产品介绍 | Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] SWISS: Q5JUK3 Gene ID: 57582 |
| 产品图片 |  The purity of the protein is greater than 85% as determined by reducing SDS-PAGE. |
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