pSEVA341 BioVector® Plasmid低拷贝克隆载体-BioVector NTCC质粒载体菌株细胞蛋白抗体基因保藏中心
- 价 格:¥59850
- 货 号:BioVector® pSEVA341
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
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BioVector® pSEVA341 Plasmid低拷贝克隆载体
pSEVA341 is a member of the Standard European Vector Architecture (SEVA) collection of plasmids. These plasmids are designed to be highly standardized and compatible, facilitating genetic engineering and synthetic biology research.
Key Features:
Origin of Replication (ColE1): Allows the plasmid to replicate in E. coli.
Chloramphenicol Resistance Gene (CmR): Confers resistance to the antibiotic chloramphenicol, enabling selection of bacteria carrying the plasmid.
Multiple Cloning Site (MCS): Contains a variety of restriction enzyme recognition sites, allowing for the insertion of foreign DNA fragments.
Standardized Structure: Adheres to the SEVA architecture, promoting compatibility and interchangeability of genetic parts.
Applications:
Gene cloning and expression: Introducing foreign genes into E. coli for heterologous protein production.
Synthetic biology: Constructing genetic circuits and pathways for various applications.
Biotechnology: Developing new tools and technologies for industrial and medical applications.
Advantages:
Standardization: The SEVA architecture ensures compatibility and interchangeability of genetic parts.
Versatile cloning: The MCS allows for flexible insertion of DNA fragments.
Well-characterized: The properties of SEVA plasmids are well-documented, facilitating their use in research.
Limitations:
Limited copy number: The copy number of pSEVA341 in E. coli may be relatively low, which can limit protein expression levels.
Conclusion:
pSEVA341 is a valuable tool for researchers working in synthetic biology, biotechnology, and other fields. Its standardized design and versatility make it a popular choice for a wide range of applications.
Keywords: pSEVA341, SEVA plasmids, genetic engineering, synthetic biology, gene cloning, protein expression
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