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
- 保存条件:
常温
- 保质期:
三年
- 英文名:
pECFP-ER
- 库存:
现货
- 供应商:
上海盖宁生物
| 质粒类型: | 荧光蛋白报告载体 |
|---|---|
| 启动子: | CMV |
| 克隆方法: | 多克隆位点,限制性内切酶 |
| 载体大小: | 4769 bp |
| 载体抗性: | Kanamycin (卡那霉素) |
| 筛选标记: | Neomycin (新霉素) |
订购信息
| 产品编号 | 产品名称 | 规格 | 价格 |
|---|---|---|---|
| 1131 | pECFP-ER | 5ug质粒 |
¥1000.00 |
质粒图谱
载体描述
pECFP-ER encodes a fusion protein consisting of enhanced cyan fluorescent protein (ECFP); the endoplasmic reticulum (ER) targeting sequence of calreticulin (1) cloned at the 5' end; and the sequence encoding the ER retrieval sequence, KDEL (2, 3), cloned at the 3' end. ECFP-ER is a soluble protein that localizes in the lumen of the ER in transfected cells. ECFP's fluorescence excitation maxima (major peak at 433 nm and a minor peak at 453 nm) and emission maxima (major peak at 475 nm and a minor peak at 501 nm) are similar to other cyan emission variants (4–6). ECFP also contains mutations to enhance the brightness and solubility of the protein, primarily due to improved protein-folding properties and efficiency of chromophore formation (5, 7, 8).
In addition to the chromophore mutations, ECFP contains more than 190 silent base changes that correspond to human codon-usage preferences (9). SV40 polyadenylation signals downstream of the ECFP-ER fusion direct proper processing of the 3' end of the mRNA. The vector backbone also contains an SV40 origin for replication in mammalian cells expressing the SV40 T-antigen. A neomycin resistance cassette (Neor) consisting of the SV40 early promoter, the neomycin/ kanamycin resistance gene of Tn5, and polyadenylation signals from the herpes simplex virus thymidine kinase (HSV-TK) gene allow stably transfected eukaryotic cells to be selected using G418 (10). A bacterial promoter upstream of this cassette drives expression of the gene encoding kanamycin resistance in E. coli. The pECFP-ER backbone also provides a pUC origin of replication for propagation in E. coli and an f1 origin for single-stranded DNA production.
载体应用
The pECFP-ER Vector is designed for fluorescent labeling of the endoplasmic reticulum in mammalian cells (11, 12). Fluorescence can be oserved in living cells by microscopy. pECFP-ER can be introduced into mammalian cells using any standard transfection method. If required, stable transformants can be selected using G418 (10). Filter sets are available for dual-color detection of EYFP and ECFP using conventional epifluoresence microscopy (13). Please refer to the Living Colors® User Manual, provided with this vector, for additional information.
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*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.
Nature 深度剖析:管坤良与 Alj 组研究成果为何截然相反,Hippo 通路调控乳腺癌的两面性
3 日,Mohamed Bentires-Alj 课题组于 Nature 发表回应,提出了可能导致双方如此迥异的实验结果的原因: 1. 第一个焦点集中于使用 CRISPR 敲除和 shRNA 敲低 LATS1/2 所带来的差异。Bentires-Alj 组发现,shRNA 载体慢病毒高滴度感染细胞会迟滞其生长,但根据原文结果,LATS1/2 表达量应该与 ERα 表达量负相关,降低 LATS1/2 表达量应该会使细胞生长加快。这表明中等程度的降低 LATS1/2 的表达量和大幅降低乃至敲除 LATS
【求助】关于构建目的基因启动子序列的虫荧光素酶报告基因重组质粒的问题请教
longgyin8341 最近想做虫荧光素酶报告基因,但是从来没有做过,想求院子里高手指教: 我是要观察一种药物是否能作用于细胞内的几种核受体(NFkB,PPAR,ER(目前还不清楚究竟是哪个,需要分别试验))的启动子区域,影响这几个核受体的转录水平,从而影响细胞的一些功能(比如凋亡等)。计划将这三种核受体的启动子区域分别扩增出来,然后与虫荧光素酶(或其他报告基因)构建重组质粒。再分别转染细胞,加入药物处理,观察荧光素酶的活性,以探索药物是否
pECFP-C pEGFP-C-5’ pECFP-C-3' pECFP-N1 pEGFP-N-5’ pEGFP-N-3’ pEF/myc/ER pEF-F pCDNA3.1R pEGFP-C(KAN+) pEGFP-C-5’ pEGFP-C-3' pEGFP-N(KAN+) pEGFP-N-5’ pEGFP-N-3’ pENTR/D-TOPO(KAN+) M13F M13R pET-*(His)(KAN+) T7 T7 Ter pET22(a,b,c)(AMP+) T7 T7 Ter
技术资料暂无技术资料 索取技术资料







