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Rapid modification of the pET-28 expression vector for ligation independent cloning using homologous recombination in Saccharomyces cerevisiae

The ability to rapidly customize an expression vector of choice is a valuable tool for any researcher involved in high-throughput molecular cloning for protein overexpression. Unfortunately, it is common practice to amend or neglect protein targets if the gene that encodes the protein of interest is...

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Bibliografische gegevens
Gepubliceerd in:Plasmid
Hoofdauteurs: Gay, Glen, Wagner, Drew T., Keatinge-Clay, Adrian T., Gay, Darren C.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2014
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4388760/
https://ncbi.nlm.nih.gov/pubmed/25304917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.plasmid.2014.09.005
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