| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 14110 | Biomolecular Engineering | 2006 | 4 Pages | 
Abstract
												The PCR primers used for cloning of evolutionary conserved genes or homologous DNA sequences are usually guessmer oligonucleotides. We introduce a simple way using Pfu polymerase to overcome possible PCR amplification failure because of 3′-end mismatches of guessed primers with the target DNA.
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											Authors
												Fakhraddin Naghibalhossaini, Afsaneh Moaddeb, 
											