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- 详细信息
- 文献和实验
- 技术资料
- 服务名称:
大肠杆菌系统重组蛋白表达
- 提供商:
普健生物(武汉)科技有限公司
Uniprot号:Q64324
基因名:Stxbp2
蛋白名:Syntaxin-binding protein 2
蛋白别名:
Syntaxin-binding protein 2, MUSEC1, Protein unc-18 homolog 2, Munc18-2, Unc18-2, Protein unc-18 homolog B, Unc-18B
服务内容:
| 服务项目 | 客户提供 | 服务内容 | 服务周期 | 交付内容 |
|---|---|---|---|---|
| 大肠杆菌系统 蛋白表达 |
基因序列 | 方案沟通 | 1天 | 方案报告 |
| 密码子优化和基因合成 | 5天 | 基因合成报告 | ||
| 表达纯化测试 | 3天 | 表达纯化测试报告 | ||
| 1L表达及纯化 | 3天 | 蛋白样品(3-5mg)及报告 | ||
| 放大发酵及纯化 | 7天 | 纯化的蛋白及报告 |
案例展示:

Stxbp2相关研究文献:
1. Pediatric hemophagocytic lymphohistiocytosis. [32107531]
2. STING activation in platelets aggravates septic thrombosis by enhancing platelet activation and granule secretion. [36944334]
3. A Rare STXBP2 Mutation in Severe COVID-19 and Secondary Cytokine Storm Syndrome. [35207437]
4. Prognostic analysis and validation of diagnostic marker genes in patients with osteoporosis. [36311708]
5. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. [29266534]
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文献和实验2. STING activation in platelets aggravates septic thrombosis by enhancing platelet activation and granule secretion. [36944334]
3. A Rare STXBP2 Mutation in Severe COVID-19 and Secondary Cytokine Storm Syndrome. [35207437]
4. Prognostic analysis and validation of diagnostic marker genes in patients with osteoporosis. [36311708]
5. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. [29266534]
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