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当前位置: 首页 > 产品中心 > Specialty_ELISA_kits > 牛津遗传学/pSF-CMV-COOH-EKT-His2(OG67)C端His标记质粒/OG67/1 Ea
商品详细牛津遗传学/pSF-CMV-COOH-EKT-His2(OG67)C端His标记质粒/OG67/1 Ea
牛津遗传学/pSF-CMV-COOH-EKT-His2(OG67)C端His标记质粒/OG67/1 Ea
牛津遗传学/pSF-CMV-COOH-EKT-His2(OG67)C端His标记质粒/OG67/1 Ea
商品编号: OG67
品牌: oxgene
市场价: ¥5033.80
美元价: 3020.28
产地: 美国(厂家直采)
公司:
产品分类: 特色ELISA试剂盒
公司分类: Specialty_ELISA_kits
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Plasmid Info:

Plasmid Information

Product Name: pSF-CMV-COOH-EKT-His2

Product Code: OG67

Size (bp): 4269 bp

Bacterial Antibiotic Selection: KanR

Origin and Compatibility: pUC high copy derived from pBR322

Bacterial Copy Number: 500-700 per cell

Promoter: Cytomegalovirus (CMV) immediate early promoter

Plasmid Purpose:

This vector adds a His tag that allows protein purification by binding to metal matrices such as nickel. The His tag will be positioned at the 3 prime end (C terminus) of a gene (expressed protein) in the primary MCS (NotI to XbaI). The His tag coding sequence contains six histidine residues that is downstream of a short glycine spacer and an enterokinase cleavage site (DDDDK) that can be used to remove the tag from a purified protein if required. It cleaves after the lysine residue.

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. For this reason we stock a range of other promoters that are compatible with this plasmid and are available on request.

Sequence and Map:

Other Info:

Transcription Termination:

This plasmid contains three alternative transcription terminators for mammalian bacterial and bacteriophage (T7) expression. This means that only the promoter needs to be changed to alter the expression system you are using. We sell multiple promoters that can be used in each of these systems. The presence of each terminator does not reduce expression in the alternative systems.

Cloning:

Cloning in a Gene:

There is a start codon in the NcoI site can be removed by digestion with KpnI if required. The MCS for gene insertions extends from NotI to XbaI. There are built in Shine-Dalgarno and KOZAK sequences aligned with the start codon within the NcoI restriction site. If these are removed you will need to add a ribosomal entry site to the 5 prime end of your gene for optimal expression.

IP Status:

Intellectual Property Status

This product is part of our SnapFast plasmid range, for more information on the Intellectual property status of this plasmid please click here

品牌介绍
OXGENE的技术平台和专家解决方案加速了细胞和基因疗法的发现,开发和制造。我们解决了现代生物学中基因治疗,抗体治疗和基因编辑方面最重要和最具挑战性的问题。我们的技术可以实现精确而强大的哺乳动物细胞工程。我们以自动化和信息学为导向的方法意味着我们解决了其他人无法推进新疗法交付的问题。