Integration of PCR fragments at any specific site within cloning vectors without the use of restriction enzymes and DNA ligase

Here, we describe a method that offers a unique way to engineer plasmids with precision but without digestion using restriction enzymes for the insertion of DNA. The method allows the insertion of PCR fragments in between any two nucleotides within a target plasmid. The only requirement is that the...

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Détails bibliographiques
Publié dans:BioTechniques. - 1991. - 31(2001), 1 vom: 12. Juli, Seite 88-90, 92
Auteur principal: Geiser, M (Auteur)
Autres auteurs: Cèbe, R, Drewello, D, Schmitz, R
Format: Article
Langue:English
Publié: 2001
Accès à la collection:BioTechniques
Sujets:Technical Report Journal Article DNA Primers DNA Restriction Enzymes EC 3.1.21.- DNA Ligases EC 6.5.1.-