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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:A2AAY5
基因名:Sh3pxd2b
蛋白名:SH3 and PX domain-containing protein 2B
蛋白别名:
SH3 and PX domain-containing protein 2B, Factor for adipocyte differentiation 49, Tyrosine kinase substrate with four SH3 domains
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:

Sh3pxd2b相关研究文献:
1. Comprehensive bioinformatics and experimental analysis of SH3PXD2B reveals its carcinogenic effect in gastric carcinoma. [37211344]
2. Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature. [39660974]
3. Human Genetics of Ventricular Septal Defect. [38884729]
4. Sh3pxd2b mice are a model for craniofacial dysmorphology and otitis media. [21818352]
5. Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome. [34538861]
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文献和实验2. Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature. [39660974]
3. Human Genetics of Ventricular Septal Defect. [38884729]
4. Sh3pxd2b mice are a model for craniofacial dysmorphology and otitis media. [21818352]
5. Novel SH3PXD2B variant identified by whole-exome sequencing in a Turkish newborn with Frank-Ter Haar Syndrome. [34538861]
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