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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:C8YR32
基因名:Loxhd1
蛋白名:Lipoxygenase homology domain-containing protein 1
蛋白别名:
Lipoxygenase homology domain-containing protein 1
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:

Loxhd1相关研究文献:
1. LOXHD1 is indispensable for maintaining TMC1 auditory mechanosensitive channels at the site of force transmission. [39256406]
2. Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. [33892339]
3. Loxhd1 Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells. [33707295]
4. Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs' endothelial corneal dystrophy. [37441688]
5. LOXHD1 is an oncofusion-regulated antigen of ewing sarcoma. [40234527]
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文献和实验2. Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. [33892339]
3. Loxhd1 Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells. [33707295]
4. Systematic review of SLC4A11, ZEB1, LOXHD1, and AGBL1 variants in the development of Fuchs' endothelial corneal dystrophy. [37441688]
5. LOXHD1 is an oncofusion-regulated antigen of ewing sarcoma. [40234527]
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