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scarabgenomics/10X MOPS Buffer for EZ Rich Defined E. coli Growth Medium/D-0508-10

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面议
货号:D-0508-10
浏览量:127
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的D-0710-100-10倍改良Korz培养基,100毫升 ***** 1个D-0710-1LK-10X改良Korz培养基,1000毫升 ***** 1个可重现的结果 –使用已知所有成分的特定培养基,而不是包含酵母提取物或酪蛋白水解物的不确定培养基,可以使结果紧密复制。降低监管负担 -由于Korz不包含任何动物来源的成分,因此不需要原产地证明。降低风险 –消除不确定的成分可大大降低与复杂生物相关的过程相关杂质的风险。为了简化基本培养基的使用,圣甲虫基因组公司提供了一个包含10倍改良Korz培养基和单独的50倍硫酸镁溶液的两组分试剂盒。将浓缩的基本培养基和相关的硫酸镁溶液稀释以创建1X培养基。然后必须添加碳源以支持细胞生长。我们建议使用相当于0.2%的葡萄糖。稀释的1X培养基(含碳源和适当的抗生素)用于摇瓶中的表达优化。在分批补料发酵中,相同的培养基也可用作“分批”阶段的培养基。通常,将碳源的水平调节至比摇瓶中使用的水平更高的水平,例如,当使用葡萄糖时,葡萄糖水平将增加至0.5%。圣甲虫的CleanGenome®菌株是专门为生产生物治疗性蛋白质和DNA而设计的。用于生物治疗生产的“最清洁”培养基是化学定义的最小培养基。因此,改良的Korz基本培养基已使用Scarab CleanGenome®菌株进行了广泛测试,以验证其支持细胞生长和重组蛋白生产的能力。Korz基本培养基最初被设计用于大肠杆菌的高密度分批补料发酵(Korz 等。1995)。培养基由磷酸盐缓冲液,镁,柠檬酸铁,微量元素组成。用户需要提供碳源。用于优化摇瓶表达的相同基础培养基也可用于分批补料发酵,从而在两个过程之间提供连续性。在分批补料发酵中,相同的培养基仅补充了较高的碳源含量。