Direct cloning of unmodified PCR products by exploiting an engineered restriction site
- 27 May 1994
- Vol. 143 (1) , 151-152
- https://doi.org/10.1016/0378-1119(94)90623-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- New vectors for direct cloning of PCR productsGene, 1994
- New vectors for direct cloning of PCR productsGene, 1993
- Construction of new T vectors for direct cloning of PCR productsGene, 1993
- 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
- Ligation-independent cloning of PCR products (LIC-PCR)Nucleic Acids Research, 1990
- A simple method for site-directed mutagenesis using the polymerase chain reactionNucleic Acids Research, 1989
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerasesNucleic Acids Research, 1988
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985