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- 湖北省武汉市
- 斑马鱼slc10a7 zgc:92251重组蛋白表达
- 2025年07月01日
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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：Q6DHK8
基因名：slc10a7 zgc:92251
蛋白名：Sodium/bile acid cotransporter 7 (Na(+)/bile acid cotransporter 7) (Solute carrier family 10 member 7)
蛋白别名：
Sodium/bile acid cotransporter 7, Na(+)/bile acid cotransporter 7, Solute carrier family 10 member 7, slc10a7, zgc:92251
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 |
如果您对哺乳动物细胞(HEK293细胞和CHO细胞)，昆虫细胞(Sf9/Hi5) Bac-to-Bac系统，毕赤酵母(Pichia pastoris, GS115, X33, KM71)，酿酒酵母(Saccharomyces cerevisiae, BY4741, INVSc1)和枯草芽孢杆菌(Bacillus subtilis, BS168, WB800N)表达此蛋白感兴趣，欢迎留言咨询。
案例展示：
slc10a7 zgc:92251相关研究文献：
1. SLC10A7, an orphan member of the SLC10 family involved in congenital disorders of glycosylation. [34999954]
2. Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine. [38037133]
3. SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. [30082715]
4. The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling. [32350310]
5. Circular RNA circHECTD1 facilitates glioma progression by regulating the miR-296-3p/SLC10A7 axis. [33561315]
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