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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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Hlavní autoři: Linn, T, St Pierre, R
Médium: Artigo
Jazyk:Inglês
Vydáno: 1990
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC208539/
https://ncbi.nlm.nih.gov/pubmed/2137119
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