General method for direct cloning of DNA fragments generated by the polymerase chain reaction
Open Access
- 1 January 1991
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 19 (16) , 4560
- https://doi.org/10.1093/nar/19.16.4560
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- A Universal Method for the Direct Cloning of PCR Amplified Nucleic AcidNature Biotechnology, 1991
- A simple and efficient method for direct cloning of PCR products using ddT-tailed vectorsNucleic Acids Research, 1991
- Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR productsNucleic Acids Research, 1991
- Restriction endonuclease cleavage at the termini of PCR products.1990
- Efficient cloning of PCR generated DNA containing terminal restriction endonuclease recognition sitesNucleic Acids Research, 1990
- Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerasesNucleic Acids Research, 1988