Efficient cloning of PCR generated DNA con... [Nucleic Acids Res. 1990] - PubMed

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Cloning of polymerase chain reaction-generated DNA containing terminal restriction endonuclease recognition sites. [Methods Enzymol. 1993]
Cloning of polymerase chain reaction-generated DNA containing terminal restriction endonuclease recognition sites.
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Digestion of terminal restriction endonuclease recognition sites on PCR products. [Biotechniques. 1998]
Digestion of terminal restriction endonuclease recognition sites on PCR products.
Zimmermann K, Schögl D, Mannhalter JW. Biotechniques. 1998 Apr; 24(4):582-4.
A T-linker strategy for modification and directional cloning of PCR products. [Methods Mol Biol. 1997]
A T-linker strategy for modification and directional cloning of PCR products.
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Review Cloning PCR products. An overview.
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Quantitative assessment on the cloning efficiencies of lentiviral transfer vectors with a unique clone site. [Sci Rep. 2012]
Quantitative assessment on the cloning efficiencies of lentiviral transfer vectors with a unique clone site.
Zhang G, Tandon A. Sci Rep. 2012; 2:1-8. Epub 2012 May 22.
DISEC-TRISEC: di- and trinucleotide-sticky-end cloning of PCR-amplified DNA. [Nucleic Acids Res. 1993]
DISEC-TRISEC: di- and trinucleotide-sticky-end cloning of PCR-amplified DNA.
Dietmaier W, Fabry S, Schmitt R. Nucleic Acids Res. 1993 Jul 25; 21(15):3603-4.
In vivo cloning of PCR products in E. coli. [Nucleic Acids Res. 1993]
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Efficient cloning of PCR generated DNA containing terminal restriction endonucle...
Efficient cloning of PCR generated DNA containing terminal restriction endonuclease recognition sites.
Nucleic Acids Res. 1990 Oct 25 ;18(20):6156.

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