Minimal cross-recombination between wild-type and loxP511 sites in vivo facilitates truncating both ends of large DNA inserts in pBACe3.6 and related vectors

Minimal cross-recombination between wild-type and loxP511 sites in vivo facilitates truncating both ends of large DNA inserts in pBACe3.6 and related vectors

Contrary to several earlier reports, we find that cross-recombination between wild-type and the mutant loxP511 sites is

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nucleic acids research 2005-01, Vol.33 (13), p.e118-e118
Hauptverfasser: Shakes, Leighcraft A., Garland, Douglas M., Srivastava, Deepak K., Harewood, Ken R., Chatterjee, Pradeep K.
Format: Artikel
Sprache:eng
Schlagworte:
Bacteriophage P1 - genetics
Base Sequence
Chromosomes, Artificial, Bacterial
Deoxyribonucleases, Type II Site-Specific - metabolism
DNA - chemistry
DNA Primers
DNA Transposable Elements
Integrases - metabolism
Methods Online
Mutagenesis, Insertional
Plasmids
Recombination, Genetic
Regulatory Sequences, Nucleic Acid
Sequence Deletion
Transduction, Genetic
Viral Proteins - metabolism
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Contrary to several earlier reports, we find that cross-recombination between wild-type and the mutant loxP511 sites is
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/gni119