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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:
pEGFP-C3
- 库存:
60
- 供应商:
信裕生物
- 规格:
5ug质粒
基本信息
| 质粒类型: | 荧光蛋白报告载体 |
|---|---|
| 启动子: | CMV |
| 表达水平: | 高 |
| 克隆方法: | 多克隆位点,限制性内切酶 |
| 载体大小: | 4727 bp (查看载体序列) |
| 5' 测序引物及序列: | pEGFP-C: 5'-CATGGTCCTGCTGGAGTTCGTG-3' |
| 3' 测序引物及序列: | pEGFP-C-3: 5'-TATGGCTGATTATGATCAGT-3'; pEGFP-C1-R: 5'-CTACAAATGTGGTATGGCTG-3' |
| 载体标签: | N-EGFP |
| 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 |
|---|---|---|---|
| XY1109 | pEGFP-C3 | 5ug质粒 |
¥1000.00 |
质粒图谱
载体描述
pEGFP-C3 encodes a red-shifted variant of wild-type GFP (1–3) which has been optimized for brighter fluorescence and higher expression in mammalian cells. (Excitation maximum = 488 nm;emission maximum = 507 nm.) pEGFP-C3 encodes the GFPmut1 variant (4) which contains the double-amino-acid substitution of Phe-64 to Leu and Ser-65 to Thr. The coding sequence of the EGFP gene contains more than 190 silent base changes which correspond to human codon-usage preferences (5). Sequences flanking EGFP have been converted to a Kozak consensus translation initiation site (6) to further increase the translation efficiency in eukaryotic cells. The MCS in pEGFP-C3 is between the EGFP coding sequences and the SV40 poly A. Genes cloned into the MCS will be expressed as fusions to the C terminus of EGFP if they are in the same reading frame as EGFP and there are no intervening stop codons. SV40 poly adenylation signals downstream of the EGFP gene direct proper processing of the 3' end of the EGFP mRNA. The vector backbone also contains an SV40 origin for replication in mammalian cells expressing the SV40 T-antigen. Aneomycin resistance cassette (Neor), consisting of the SV40 early promoter, the neomycin/kanamycin resistance gene of Tn5, and poly adenylation signals from the Herpes simplex virus thymidine kinase (HSV TK) gene, allows stably transfected eukaryotic cells to be selected using G418. A bacterial promoter upstream of this cassette expresses kanamycin resistance in E. coli. The pEGFP-C3 backbone also provides a pUC origin of replication for propagation in E. coli and an f1origin for single-stranded DNA production.
载体应用
Fusions to the C terminus of EGFP retain the fluorescent properties of the native protein allowing the localization of the fusion protein in vivo. The target gene should be cloned into pEGFP-C3 so that it is in frame with the EGFP coding sequences, with no intervening in-frame stop codons. The recombinant EGFP vector can be transfected into mammalian cells using any standard transfection method. If required, stable transformants can be selected usingG418 (7). pEGFP-C3 can also be used simply to express EGFP in a cell line of interest (e.g., as a transfection marker).
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文献和实验maoliping70:pEGFP-N1为载体表达的核蛋白要确证表达于核内的方法为用PI染色,PI只与核酸结合,在488nm激发下发红光,而GFP发绿光,红光与绿光重叠发黄光。还有以下疑问:1.作为对照的pEGFP-N1空载体转染细胞后表达的GFP蛋白为27KD,能自由通过核孔复合体,也就是说GFP在核内也有表达,那会与PI重叠发黄光影响测定吗?2.有提出GFP在细胞固定时,会从细胞漏出,那细胞本身表达的浆蛋白若分子量小,也会漏出吗?还是因为有定位信号而不漏出?3.细胞固定用的70%乙醇是直接
ono1180 求助各位同道: 我想过表达一个基因,想选用一个质粒载体连接此基因再转染入细胞,选用的载体需要有绿色荧光标记,而且能筛选出稳定转染的细胞系,上网查了一下觉得pEGFP系列的好像符合我的要求。 请问这个载体怎么样,大家还有什么载体觉得挺好,请指教,感谢了。 xiaokangkuaile 我用的是pEGFP-C1表达载体,但我的目的基因对GFP表达有影响,转染效果很差
判断连接方向,可以通过两种方法:1、PCR,两条引物中一条是载体上的通用引物,另一条是扩增目的片段时用的引物 2、酶切,使用SalI酶和目的片段中的一个酶切位点做双酶切,根据条带大小判断插入方向。 lf2003128245 谢谢!我也是准备用pEGFP质粒来做,请问你有这个质粒的序列吗?我在网上没有找到。 lf2003128245 也要谢谢上面的那位大侠,可能是我表述的不清楚,把几个问题搞在一起了,让你没明白
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