Preparation of Genomic DNA from Plant Tissue
Open Access
- 1 July 1994
- journal article
- unit
- Published by Wiley in Current Protocols in Molecular Biology
- Vol. 27 (1) , 2.3.1-2.3.7
- https://doi.org/10.1002/0471142727.mb0203s27
Abstract
This unit describes two methods for preparing genomic DNA from plant tissue. In the first method, plant cells are lysed with ionic detergent, treated with protease, and subsequently purified by cesium chloride (CsCl) density gradient centrifugation. The second method is based upon a series of treatments with the nonionic detergent cetyltrimethylammonium bromide (CTAB) to lyse cells and purify nucleic acid. Nucleic acid is recovered from the final CTAB solution by isopropanol or ethanol precipitation. The first method, although somewhat more lengthy, results in highly purified nucleic acid. The second method requires fewer manipulations, results in very high yields (˜10-fold higher per gram fresh tissue depending on species and condition of starting material), and produces DNA that is less pure but nonetheless suitable in quality for use in many molecular biology manipulations.Keywords
This publication has 5 references indexed in Scilit:
- Purification and restriction endonuclease analysis of plant nuclear DNAPublished by Elsevier ,1986
- Extraction of DNA from milligram amounts of fresh, herbarium and mummified plant tissuesPlant Molecular Biology, 1985
- A plant DNA minipreparation: Version IIPlant Molecular Biology Reporter, 1983
- Rapid isolation of high molecular weight plant DNANucleic Acids Research, 1980
- The isolation of bacterial nucleic acids using cetyltrimethylammonium bromide (Cetavlon)Biochimica et Biophysica Acta, 1953