The David Waugh Lab has deposited plasmids at Addgene for distribution to the research community. Addgene is a non-profit plasmid repository dedicated to improving life science research.
Learn more about research in the David Waugh Lab.
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|Isolation of Metarhizium anisopliae carboxypeptidase A with native disulfide bonds from the cytosol of Escherichia coli BL21(DE3).||Austin et al|
|The substrate specificity of Metarhizium anisopliae and Bos taurus carboxypeptidases A: insights into their use as tools for the removal of affinity tags.||Austin et al|
|Gateway vectors for the production of combinatorially-tagged His6-MBP fusion proteins in the cytoplasm and periplasm of Escherichia coli.||Nallamsetty et al|
|Efficient site-specific processing of fusion proteins by tobacco vein mottling virus protease in vivo and in vitro.||Nallamsetty et al|
|Maltodextrin-binding proteins from diverse bacteria and archaea are potent solubility enhancers.||Fox et al|
|The P1' specificity of tobacco etch virus protease.||Kapust et al|
|Tobacco etch virus protease: mechanism of autolysis and rational design of stable mutants with wild-type catalytic proficiency.||Kapust et al|
|Controlled intracellular processing of fusion proteins by TEV protease.||Kapust et al|
|Site-specific, enzymatic biotinylation of recombinant proteins in Spodoptera frugiperda cells using biotin acceptor peptides.||Duffy et al|
|A versatile plasmid expression vector for the production of biotinylated proteins by site-specific, enzymatic modification in Escherichia coli.||Tsao et al|