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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:O56860
基因名:p3
蛋白名:p3
蛋白别名:
Gag polyprotein, Gag protein, gag, p3, p3Gag, p48Gag
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:

p3相关研究文献:
1. Characterization of the genome of feline foamy virus and its proteins shows distinct features different from those of primate Spumaviruses. [9261397]
2. Specific interaction of a novel foamy virus Env leader protein with the N-terminal Gag domain. [11483744]
3. Features of the Env leader protein and the N-terminal Gag domain of feline foamy virus important for virus morphogenesis. [12781711]
4. N-terminal Gag domain required for foamy virus particle assembly and export. [16160174]
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文献和实验2. Specific interaction of a novel foamy virus Env leader protein with the N-terminal Gag domain. [11483744]
3. Features of the Env leader protein and the N-terminal Gag domain of feline foamy virus important for virus morphogenesis. [12781711]
4. N-terminal Gag domain required for foamy virus particle assembly and export. [16160174]
Development of Foamy Virus Vectors
8 ). In an effort to address these issues, two other retro viruses have been explored for their gene transfer potential; lentiviruses, like the human immunodeficiency virus (HIV) and, to a lesser extent, foamy (or spuma) viruses (9 ,10 ). Although many details
亦称泡沫因子( foamy agent)。是具包膜的直径为 100— 140毫微米的球状病毒。一般认为属于致癌 RNA病毒。它是 RNA型病毒,它具有 RNA依存性的 DNA聚合酶。在猴肾组织培养中作为内在的地引起细胞变性效应的因子, 1954年由恩德斯( J. Ende-rs)和皮布尔斯( T. Peebles)分离得到,其后又从牛、猫、仓鼠等的正常乃至病变组织中分离到此病毒。虽也怀疑它存在于人体中,但无确证。在感染各种哺乳类的组织培养细胞时,能引起具有液胞的多核细胞特征的细胞
Construction and Analysis of Genomic, Full-Length Infectious Foamy Virus DNA Clones
The molecular engineering of recombinant plasmid DNA clones containing the full-length and replication-competent feline foamy (retro)virus (FFV) proviral genome is described. The methods used to combine subgenomic FFV DNA fragments
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