Step-by-step efficiency of cloning, small-scale protein expression and

Step-by-step efficiency of cloning, small-scale protein expression and

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Download scientific diagram | Step-by-step efficiency of cloning, small-scale protein expression and purification of 271 conserved proteins of E. coli. A total of 220 purified proteins with high and moderate yields were subjected to large-scale expression. Afterwards, 176 proteins could be purified with a minimum of 500 g. Overall, 34 target proteins were subjected to Gateway recombination cloning to express fusion proteins with maltose binding protein, glutathione S-transferase, and N-utilizing substance A, respectively. Overall, 21 proteins fused to maltose binding protein were purified with a minimum of 500 g. ECHH, E. coli-human-homologues; LUCA, Last Common Universal AncestorDownload Power Point slide (282 KB) from publication: Identification of the predominant antigenic epitopes in intestinal flora in IBD | The normal intestinal flora is required for the development of intestinal inflammation in animal models of inflammatory bowel disease (IBD). In humans, several studies indicated a potential association of Escherichia coli (E. coli) with IBD. In addition, we have shown that | Inflammatory Bowel Disease, epitopes and Gastrointestinal Microbiome | ResearchGate, the professional network for scientists.

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Addgene: Plasmid Cloning by PCR (with Protocols)

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A Simple Cloning-free Method to Efficiently Induce Gene Expression

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A Protein-Engineered, Enhanced Yeast Display Platform for Rapid

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Protein Expression Systems

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An efficient protocol to enhance recombinant protein expression

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Recombinant Protein Expression Protocols and Methods

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Expression vector - Wikipedia

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Protein Expression Systems

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Learn about Recombinant Protein Production

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Schematic overview of established workflow used in this study to

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Expresso® Cloning and Expression Systems: Expressioneering

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Protein Expression Systems

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Cloning Genes-of-Interest into a Plasmid Vector

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Choosing a Bacterial Strain for your Cloning Application

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Protein engineering utilizing an E. coli expression system. The