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New high-cloning-efficiency vectors for complementation studies and recombinant protein overproduction in Escherichia coli and Salmonella enterica

Galloway et al. recently described a method to alter vectors to include Type IIS restriction enzymes for high efficiency cloning. Utilizing this method, the multiple cloning sites of complementation and overexpression vectors commonly used in our laboratory were altered to contain recognition sequen...

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Dettagli Bibliografici
Pubblicato in:Plasmid
Autori principali: VanDrisse, C.M., Escalante-Semerena, J.C.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5126758/
https://ncbi.nlm.nih.gov/pubmed/27234933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.plasmid.2016.05.001
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