- ￥2000 - 8000
- 湖北省武汉市
- Mouse Ndufa13重组蛋白表达
- 2025年09月14日
企业认证
相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 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：Q9ERS2
基因名：Ndufa13
蛋白名：NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13
蛋白别名：
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 13, Cell death regulatory protein GRIM-19, Complex I-B16.6, CI-B16.6, Gene associated with retinoic and interferon-induced mortality 19 protein, GRIM-19, Gene associated with retinoic and IFN-induced mortality 19 protein, NADH-ubiquinone oxidoreductase B16.6 subunit
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：
Ndufa13相关研究文献：
1. The role of STAT3 in autophagy. [25951043]
2. SGK3 deficiency in macrophages suppresses angiotensin II-induced cardiac remodeling via regulating Ndufa13-mediated mitochondrial oxidative stress. [39158709]
3. Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment. [39963288]
4. Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. [32722639]
5. [Pathogenic role of NDUFA13 inactivation in spontaneous hepatitis in mice and the mechanism]. [33509753]
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验2. SGK3 deficiency in macrophages suppresses angiotensin II-induced cardiac remodeling via regulating Ndufa13-mediated mitochondrial oxidative stress. [39158709]
3. Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment. [39963288]
4. Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. [32722639]
5. [Pathogenic role of NDUFA13 inactivation in spontaneous hepatitis in mice and the mechanism]. [33509753]
技术资料暂无技术资料 索取技术资料
