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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：Q8HXL3
基因名：WDR62
蛋白名：WD repeat-containing protein 62
蛋白别名：
WD repeat-containing protein 62
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：
WDR62相关研究文献：
1. WDR62 Primary Microcephaly. [35188728]
2. Pathophysiological Significance of WDR62 and JNK Signaling in Human Diseases. [33937237]
3. A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature. [30706430]
4. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. [35808830]
5. WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice. [36571716]
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文献和实验该产品被引用文献
1. WDR62 Primary Microcephaly. [35188728]
2. Pathophysiological Significance of WDR62 and JNK Signaling in Human Diseases. [33937237]
3. A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature. [30706430]
4. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. [35808830]
5. WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice. [36571716]
2. Pathophysiological Significance of WDR62 and JNK Signaling in Human Diseases. [33937237]
3. A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature. [30706430]
4. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. [35808830]
5. WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice. [36571716]
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Sus scrofa WDR62重组蛋白表达
￥2000 - 8000
