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pubmed-article:2066384pubmed:abstractTextTransfection of the hepatitis B virus (HBV) genome requires the cloning of tandem HBV sequences into a plasmid vector, which is usually screened for by restriction enzyme digestion of plasmid minipreparations from at least a dozen bacterial colonies. We describe a simple alternative screening method based on in situ hybridization of bacterial colonies with a [32P]-labelled synthetic oligonucleotide which spans the head-to-tail junction site of two tandem HBV molecules. The accurate detection by the oligoprobe is confirmed by enzymatic digestion.lld:pubmed
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pubmed-article:2066384pubmed:year1991lld:pubmed
pubmed-article:2066384pubmed:articleTitleRapid screening for bacterial colonies harbouring tandem hepatitis B virus sequences by an oligonucleotide probe.lld:pubmed
pubmed-article:2066384pubmed:affiliationUnité de Recherche Sur Les Hépatites INSERM 271, Lyon, France.lld:pubmed
pubmed-article:2066384pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2066384pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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