Skip to main content

. 1992 Aug 25;20(16):4369–4370. doi: 10.1093/nar/20.16.4369

Directional cloning of PCR products using exonuclease III.

S Kaluz ¹, K Kölble ¹, K B Reid ¹

PMCID: PMC334153 PMID: 1508730

Abstract

4369

Images in this article

Image
on p.4370

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Henikoff S. Unidirectional digestion with exonuclease III in DNA sequence analysis. Methods Enzymol. 1987;155:156–165. doi: 10.1016/0076-6879(87)55014-5. [DOI] [PubMed] [Google Scholar]
Jung V., Pestka S. B., Pestka S. Efficient cloning of PCR generated DNA containing terminal restriction endonuclease recognition sites. Nucleic Acids Res. 1990 Oct 25;18(20):6156–6156. doi: 10.1093/nar/18.20.6156. [DOI] [PMC free article] [PubMed] [Google Scholar]
Kuijper J. L., Wiren K. M., Mathies L. D., Gray C. L., Hagen F. S. Functional cloning vectors for use in directional cDNA cloning using cohesive ends produced with T4 DNA polymerase. Gene. 1992 Mar 15;112(2):147–155. doi: 10.1016/0378-1119(92)90370-5. [DOI] [PubMed] [Google Scholar]
Stoker A. W. Cloning of PCR products after defined cohesive termini are created with T4 DNA polymerase. Nucleic Acids Res. 1990 Jul 25;18(14):4290–4290. doi: 10.1093/nar/18.14.4290. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES