Hsp27 Mouse Monoclonal Antibody
产品名称: Hsp27 Mouse Monoclonal Antibody
英文名称: Hsp27 Mouse Monoclonal Antibody
产品编号: K000091M
产品价格: null
产品产地: 北京市通州区马驹桥
品牌商标: solarbio
更新时间: 2025-11-13T16:50:54
使用范围: WB ICC
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Anti-Hsp27 Monoclonal Antibody
品牌:Solarbio | 货号:K000091M
英文名称 Mouse Hsp27 Monoclonal Antibody 应用2 IF ICC 克隆类型2 Monoclonal Antibody 别名 Hsp27 应用 WB,ICC 稀释比例 WB1:1000 ICC1:300 交叉反应 Human Monkey 蛋白分子量 27kDa Gene ID 3315 保存 Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment. 储存液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 66% Glycerol. 纯化方法 Affinity purification 亚型 IgG1 免疫原 Purified recombinant human Hsp27 protein fragments expressed in E.coli. 性状 Lyophilized or Liquid Swiss Prot P04792 克隆号 7E5-1F9-D9 克隆类型 Monoclonal Antibody 来源 Mouse 背景资料 The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).
| 英文名称 | Mouse Hsp27 Monoclonal Antibody |
|---|---|
| 应用2 | IF ICC |
| 克隆类型2 | Monoclonal Antibody |
| 别名 | Hsp27 |
| 应用 | WB,ICC |
| 稀释比例 | WB1:1000 ICC1:300 |
| 交叉反应 | Human Monkey |
| 蛋白分子量 | 27kDa |
| Gene ID | 3315 |
| 保存 | Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment. |
| 储存液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 66% Glycerol. |
| 纯化方法 | Affinity purification |
| 亚型 | IgG1 |
| 免疫原 | Purified recombinant human Hsp27 protein fragments expressed in E.coli. |
| 性状 | Lyophilized or Liquid |
| Swiss Prot | P04792 |
| 克隆号 | 7E5-1F9-D9 |
| 克隆类型 | Monoclonal Antibody |
| 来源 | Mouse |
| 背景资料 | The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN). |
