You are not currently logged in.
Access JSTOR through your library or other institution:
If You Use a Screen ReaderThis content is available through Read Online (Free) program, which relies on page scans. Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Preservation of Plant Samples for DNA Restriction Endonuclease Analysis
Jeff J. Doyle and Elizabeth E. Dickson
Vol. 36, No. 4 (Nov., 1987), pp. 715-722
Published by: International Association for Plant Taxonomy (IAPT)
Stable URL: http://www.jstor.org/stable/1221122
Page Count: 8
Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Preview not available
A major obstacle facing many taxonomists interested in analyzing variation at the DNA level is the preservation of their plant material, since plants are often collected far from laboratory facilities. We have studied effect of several commonly used preservation techniques on the quality of DNA isolated from preserved tissue. Chemical treatments (FAA, ethanol, Carnoy's solution, chloroform-ethanol) all result in DNA degradation; drying tissue, on the other hand, preserves DNA integrity, at least over a several month period. High molecular weight DNA suitable for restriction endonuclease digestion and analysis by DNA hybridization was isolated from dried leaves up to two years old. This suggests that recently-prepared dried specimens may represent an alternative to fresh tissue in molecular plant systematic studies.
Taxon © 1987 International Association for Plant Taxonomy (IAPT)