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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
常温
- 保质期:
三年
- 英文名:
pLVX-IRES-tdTomato
- 库存:
现货
- 供应商:
上海盖宁生物
| 质粒类型: | 慢病毒载体 |
|---|---|
| 高拷贝/低拷贝: | 高拷贝 |
| 启动子: | CMV |
| 克隆方法: | 多克隆位点,限制性内切酶 |
| 载体大小: | 8892 bp |
| 5' 测序引物及序列: | CMV-F: CGCAAATGGGCGGTAGGCGTG |
| 载体抗性: | Ampicillin (氨苄青霉素) |
| 筛选标记: | Puromycin (嘌呤霉素) |
| 备注: | 载体能够同时表达tdTomato荧光蛋白和目的基因。 |
订购信息
| 产品编号 | 产品名称 | 规格 | 价格 |
|---|---|---|---|
| 1459 | pLVX-IRES-tdTomato | 5ug质粒 |
¥1200.00 |
质粒图谱
载体描述
pLVX-IRES-tdTomato is an HIV-1-based, lentiviral expression vector that allows the simultaneous expression of your protein of interest and tdTomato in virtually any mammalian cell type, including primary cells. tdTomato is a member of the family of fruit fluorescent proteins derived from the Discosoma sp. red fluorescent protein, DsRed (1). The vector expresses the two proteins from a bicistronic mRNA transcript, allowing tdTomato to be used as an indicator of transduction efficiency and a marker for selection by flow cytometry.
Expression of the bicistronic transcript is driven by the constitutively active human cytomegalovirus immediate early promoter (PCMV IE) located just upstream of the MCS. An encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES), positioned between the MCS and tdTomato, facilitates cap-independent translation of tdTomato from an internal start site at the IRES/tdTomato junction (1).
pLVX-IRES-tdTomato contains all of the viral processing elements necessary for the production of replication-incompetent lentivirus, as well as elements to improve viral titer, transgene expression, and overall vector function. The woodchuck hepatitis virus posttranscriptional regulatory element (WPRE) promotes RNA processing events and enhances nuclear export of viral RNA (2), leading to increased viral titers from packaging cells. In addition, the vector includes a Rev-response element (RRE), which further increases viral titers by enhancing the transport of unspliced viral RNA out of the nucleus (3). Finally, pLVX-IRES-tdTomato also contains a central polypurine tract/central termination sequence element (cPPT/CTS). During target cell infection, this element creates a central DNA flap that increases nuclear import of the viral genome, resulting in improved vector integration and more efficient transduction (4). The vector also contains a pUC origin of replication and an E. coli ampicillin resistance gene (Ampr ) for propagation and selection in bacteria.
载体应用
pLVX-IRES-tdTomato is designed to constitutively coexpress your protein of interest and tdTomato from PCMV IE when transduced into mammalian cells. Before it can be transduced into target cells, the vector must be packaged into viral particles in HEK293T cells, using our Lenti-X™ HT Packaging System (Cat. Nos. 632160 and 632161). This packaging system allows the safe production of high titer, infectious, replication-incompetent, VSV-G pseudotyped lentiviral particles that can infect a wide range of cell types, including nondividing and primary cells (5).
The presence of tdTomato allows transductants to be visualized by fluorescence microscopy and sorted by flow cytometry with standard FITC filter sets (tdTomato has an excitation maximum of 554 nm and an emission maximum of 581 nm).
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文献和实验*发表【中文论文】请标注:由上海盖宁生物科技有限公司提供;
*发表【英文论文】请标注:From Shanghai Gaining Biotechnology Co., Ltd.
sunyuzhu10 包装质粒是pMD2.G pMDLg/pRRE pRSV-Rev 过表达载体是pLVX-IRES-ZsGreen1 这样的四个质粒能包装出慢病毒么? 请有经验的战友帮忙看下 暴君 可以的 644414915 pMD2.G是VSVG吗 我现在正在包病毒,别人给了我这四个质粒,别的什么都没说,我不知道该怎么包装装染 谁有具体步骤 转染
但感觉自己包装效率还是不太高,做起来不好弄 kinguangjun 你可以考虑clontech的pLVX-ShRNA2和pLVX-IRES-ZsGreen1慢病毒系统,比invitrogen的慢病毒系统要高两个数量级以上,我们实验室一直都用这个系统。 jinanfendou 看你做什么实验了,慢病毒载体系统很多公司有卖的,但是你自己包装的话,滴度可能达不到这么高,好转染的细胞还是可以的,但是要是难转染的细胞和动物
1,tdTomato,GFP,mcherry,GFP,FP635等。 «贵公司的慢病毒载体可以插入多大的目的片段? 我们采用独特的载体设计,最大可高效包装4kb的目的片段。 «贵公司的慢病毒的安全性如何? 我们的慢病毒载体经过了一系列的改造,病毒在感染细胞中并不能自我复制,从而大大降低了其危险性。尤其是我们使用了现在最新型第四代载体系统,是目前重组系数最低的一个慢病毒包装系统,至今为止未见重组报道。慢病毒对热、去垢剂、医用消毒水、福尔马林等均很敏感,但UV照射无法
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