Three new developments in P1 cloning: Increased cloning efficiency, improved clone recovery, and a new P1 mouse library
- 31 December 1994
- journal article
- Published by Elsevier in Genetic Analysis: Biomolecular Engineering
- Vol. 11 (5-6), 171-180
- https://doi.org/10.1016/1050-3862(94)90038-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Faithful Cleavage of the P1 Packaging Site (pac) Requires Two Phage Proteins, PacA and PacB, and Two Escherichia coli Proteins, IHF and HUJournal of Molecular Biology, 1994
- Purification and DNA-Binding Activity of the PacA Subunit of the Bacteriophage P1 Pacase EnzymeJournal of Molecular Biology, 1994
- The P1 cloning system: past and futureMammalian Genome, 1994
- [47] Using bacteriophage P1 system to clone high molecular weight genomic DNAMethods in Enzymology, 1992
- Bacteriophage lysis: mechanism and regulation.Microbiological Reviews, 1992
- [2] Bacteriophage-mediated generalized transduction in Escherichia coli and Salmonella typhimuriumMethods in Enzymology, 1991
- An F factor based cloning system for large DNA fragmentsNucleic Acids Research, 1990
- HPRT-deficient (Lesch–Nyhan) mouse embryos derived from germline colonization by cultured cellsNature, 1987