| 產品編號 | bs-42191P |
| 英文名稱 | Recombinant human KCNT1 protein, N-Trx-His |
| 中文名稱 | 重組人鉀離子通道亞家族T成員1 |
| 別 名 | bA100C15.2; EIEE14; ENFL5; KCa4.1; KCNT1; KCNT1_HUMAN; Potassium channel subfamily T member 1; Potassium channel, subfamily T, member 1; SLACK. |
| 理論分子量 | 36.1kDa |
| 性 狀 | Lyophilized or Liquid |
| 濃 度 | >2mg/ml |
| 物 種 | Human |
| 序 列 | 611-780/1230 |
| 純 度 | >90% as determined by SDS-PAGE |
| 內毒素 | Not analyzed |
| 標簽 | N-Trx-His |
| 緩 沖 液 | 20mM Tris-Hcl (pH=8.0) |
| 保存條件 | Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles. |
| 注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 產品介紹 | 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 |
| 產品圖片 |  The purity of the protein is greater than 85% as determined by reducing SDS-PAGE. |
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