Improved vector system for constructing transcriptional fusions that ensures independent translation of lacZ.

An improved vector system has been developed for the in vitro construction of transcriptional fusions to lacZ. The principal feature is an RNaseIII cleavage site inserted between the polylinker cloning site and the promoterless lacZ gene. When these vectors are used to construct transcriptional fusi...

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Vydáno v:	J Bacteriol
Hlavní autoři:	Linn, T, St Pierre, R
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Microbiology (ASM) 1990
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC208539/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2137119/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.172.2.1077-1084.1990
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