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Merck

OGS97

Sigma-Aldrich

PSF-CMV-EMCV - CMV IRES PLASMID

plasmid vector for molecular cloning

别名:

cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector

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About This Item

分類程式碼代碼:
12352200
NACRES:
NA.85

形狀

buffered aqueous solution

分子量

size 4761 bp

菌種選擇

kanamycin

複製起點

pUC (500 copies)

肽切割

no cleavage

啟動子

Promoter name: CMV
Promoter activity: constitutive
Promoter type: mammalian

報告基因

none

運輸包裝

ambient

儲存溫度

−20°C

一般說明

This vector contains the internal ribosome entry site (IRES) from Encephalomyocarditis virus (EMCV) between the promoter and the multiple cloning site (MCS). It is designed to be used to express genes using cap-independent expression systems although the mRNAs produced from this vector contain a 5 prime cap. This vector is not designed for the expression of two proteins from the same mRNA. For this purpose we have designed pSF-CMV-EMCV-PciI where the PciI site contains start codons in the correct position for the IRES to express efficiently. In this vector there is an NcoI site (which contains an ATG start codon) in the correct position to enable efficient expression of a gene in the MCS. We have also developed this same vector with the T7 promoter upstream of the IRES to allow the expression of genes using T7 eukaryotic systems.

Promoter Expression Level: This plasmid contains the mammalian CMV promoter to drive gene expression. We have tested all of our mammalian promoters in a range of cell types and CMV is consistently the strongest in those we have studied. However there are many reports of the CMV promoter demonstrating silencing by methylation in long-term culture.

應用

Cloning in a gene: There is start codon within the NcoI restriction site that is positioned to allow efficient expression from the EMCV IRES. The main MCS for gene insertions in this vector therefore extends from the NcoI restriction site to the XbaI restriction site. The downstream sites (ClaI to NheI sites) have alternate functions and are used to insert other DNA sequences that we sell however they can be used to insert a gene if these functions are not required. These functions include adding peptide tags or downstream IRES elements. The BsgI and BseRI restriction sites cleave within the stop codon in the XbaI site and allow the retrospective fusion of coding sequences. These sites are normally only used on genes that we sell in the main multiple cloning site.

序列

To view sequence information for this product, please visit the product page

分析報告

To view the Certificate of Analysis for this product, please visit www.oxgene.com

相關產品

产品编号
说明
价格

儲存類別代碼

12 - Non Combustible Liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Alexander C Cerny et al.
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Recycling of signaling proteins is a common phenomenon in diverse signaling pathways. In photoreceptors of Drosophila, light absorption by rhodopsin triggers a phospholipase Cβ-mediated opening of the ion channels transient receptor potential (TRP) and TRP-like (TRPL) and generates the visual
Geoffrey M Lynn et al.
Nature biotechnology, 33(11), 1201-1210 (2015-10-27)
The efficacy of vaccine adjuvants such as Toll-like receptor agonists (TLRa) can be improved through formulation and delivery approaches. Here, we attached small molecule TLR-7/8a to polymer scaffolds (polymer-TLR-7/8a) and evaluated how different physicochemical properties of the TLR-7/8a and polymer
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Carcinogenesis, 37(1), 18-29 (2015-10-28)
Dickkopf-3 (Dkk-3) is a secreted protein whose expression is downregulated in many types of cancer. Endogenous Dkk-3 is required for formation of acini in 3D cultures of prostate epithelial cells, where it inhibits transforming growth factor (TGF)-β/Smad signaling. Here, we
Jin-Gyoung Jung et al.
PLoS genetics, 10(10), e1004751-e1004751 (2014-10-31)
The Notch3 signaling pathway is thought to play a critical role in cancer development, as evidenced by the Notch3 amplification and rearrangement observed in human cancers. However, the molecular mechanism by which Notch3 signaling contributes to tumorigenesis is largely unknown.

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