| Literature DB >> 16170214 |
Raul Tapia-Tussell1, Andres Quijano-Ramayo, Rafael Rojas-Herrera, Alfonso Larque-Saavedra, Daisy Perez-Brito.
Abstract
Genetic studies and pathogen detection in plants using molecular methods require the isolation of DNA from a large number of samples in a short time span. A rapid and versatile protocol for extracting high-quality DNA from different plant species is described. This method yields from 1 to 2 mg of DNA per gram of tissue. The absorbance ratios (A260/A280) obtained ranged from 1.6 to 2.0. A minimal presence of contaminating metabolites (as polymerase chain reaction [PCR] inhibitors) in samples and a considerable savings in reagents are characteristics of this protocol, as well as the low cost of the analysis per sample. The quality of the DNA was suitable for PCR amplification.Mesh:
Substances:
Year: 2005 PMID: 16170214 DOI: 10.1385/MB:31:2:137
Source DB: PubMed Journal: Mol Biotechnol ISSN: 1073-6085 Impact factor: 2.695