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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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Dettagli Bibliografici
Autori principali: Linn, T, St Pierre, R
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1990
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC208539/
https://ncbi.nlm.nih.gov/pubmed/2137119
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