scarabgenomics/10倍MOPS缓冲液用于富EZ定义的E。大肠杆菌培养基/D-0508-10

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货号:D-0508-10
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品牌:scarabgenomics
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商品描述

Background

Using synthetic biology methods, the Escherichia coli K-12 genome was reduced by making a series of planned, precise deletions. The multiple-deletion series (MDS™) strains (1), with genome reduction of up to 15%, were designed by identifying non-essential genes and sequences for elimination, including recombinogenic or mobile DNA and cryptic virulence genes, while preserving robust growth on rich and minimal media for either protein or plasmid production. Genome reduction also led to unanticipated beneficial properties, including high electroporation efficiency and accurate propagation of recombinant genes and plasmids that are unstable in other strains. Subsequent deletions and introduction of useful alleles produce strains suitable for many molecular biology applications. MOPS- 3-(N-morpholino) propanesulfonic acid. MOPS (pKa = 7.20) is an excellent buffer for many biological systems at near-neutral pH, MOPS Minimal is designed for culturing E. coli and works very well with our Clean Genome® strains.

Figures

Specifications

Kit Components 10X MOPS, 100mL 0.132M K2PO4, 10mL Quality Control The media is confirmed for growth of Clean Genome® Strains using liquid culture and confirmed aseptic by no growth in liquid media and agar plates. Storage Conditions Store 10X MOPS reagent at -20°C. Store 0.132M K2PO4 at room temperature.

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Support

Product Manuals 10X MOPS Buffer for EZ Rich Defined E. coli Growth Medium Papers

  1. Pósfai G, et al., (2006) Emergent properties of reduced-genome Escherichia coli. Science 312:1044-6.

Patents & Disclaimers

Products are sold for non-commercial use only, under Scarab Genomics limited use label license: Limited Label Use.Scarab is providing you with this Material subject to the non-transferable right to use the subject amount of the Material for your research at your academic institution. The Recipient agrees not to sell or otherwise transfer this Material, or anything derived or produced from the Material to a third party. NO RIGHTS ARE PROVIDED TO USE THE MATERIAL OR ANYTHING DERIVED OR PRODUCED FROM THE MATERIAL FOR COMMERCIAL PURPOSES. If the Recipient makes any changes to the chromosome of the Material that results in an invention in breach of this limited license, then Scarab will have a worldwide, exclusive, royalty-free license to such invention whether patentable or not. If the Recipient is not willing to accept the terms of this limited license, Scarab is willing to accept return of this product with a full refund, minus shipping and handling costs. For information on obtaining a license to this Material for purposes other than research, please contact Scarab’s Licensing Department. Scarab Genomics’ technology is covered by U.S. Pat. No. 6,989,265 and related foreign applications. Clean Genome® is a registered trademark of Scarab Genomics, LLC.

scarabgenomics重组蛋白生产是生命科学中使用的最强大的技术之一。产生和纯化大量靶重组蛋白的能力使多种可能性成为可能,包括其用于诊断或疾病治疗或在工业过程中的用途。乍一看,重组蛋白的表达看起来直截了当。encoding将编码所需蛋白的DNA克隆到表达载体中启动子的下游。将该克隆导入宿主细胞,细胞的蛋白质合成机制产生所需的蛋白质。但是,实际上,蛋白质表达可能会非常具有挑战性,因为可能有很多因素影响该过程。例如,某些蛋白质可能具有蛋白酶活性,这也可以通过选择表达宿主来解决。一些蛋白质可能具有有害于宿主的活性。ScarabXpress-1和ScarabExpress-2Δ之间有什么区别ScarabXpress1由ScarabXpress®T7 lac组成宿主+含有T7启动子的载体,例如pET载体。ScarabXpress2由Scarab的pSX2表达载体 + ANY CleanGenome® 大肠杆菌宿主菌株组成。