Random amplified polymorphic DNA (RAPD) interpretation requires a sensitive method for the detection of amplified DNA
- 1 January 1996
- journal article
- Published by Wiley in Electrophoresis
- Vol. 17 (10) , 1553-1554
- https://doi.org/10.1002/elps.1150171009
Abstract
The random amplified polymorphic DNA technique (RAPD) has found wide use in molecular genetics because of its speed and ease of use. For various reasons, with this method the amplified DNA fragments are produced at different concentrations between genotypes and even between polymerase chain reaction (PCR) runs. Since the detection of the multiple amplified fragments is performed routinely by agarose gel, and seldom by acrylamide gel electrophoresis, we have found that by capillary zone electrophoresis (CZE), which is more sensitive and accurate than gel electrophoresis, it is possible to unequivocally detect amplified fragments even at low concentration, avoiding polymorphism misinterpretation. CZE is also useful to make more potentially polymorphic fragments evident per random primer used, with obvious economical benefits.Keywords
This publication has 10 references indexed in Scilit:
- Impact of scoring error and reproducibility RAPD data on RAPD based estimates of genetic distanceTheoretical and Applied Genetics, 1995
- Capillary electrophoresis of DNA in uncross-linked polymer solutionsJournal of Chromatography A, 1993
- Genotype relationships inMicroseris elegans (Asteraceae, Lactuceae) revealed by DNA amplification from arbitrary primers (RAPDs)Österreichische botanische Zeitschrift, 1992
- Detection of DNA sequence polymorphisms among wheat varietiesTheoretical and Applied Genetics, 1992
- Preferential PCR amplification of alleles: mechanisms and solutions.Genome Research, 1992
- Use of single-primer DNA amplifications in genetic studies of peanut (Arachis hypogaea L.)Plant Molecular Biology, 1992
- DNA Amplification Fingerprinting Using Very Short Arbitrary Oligonucleotide PrimersNature Biotechnology, 1991
- Rapid identification of markers linked to a Pseudomonas resistance gene in tomato by using random primers and near-isogenic lines.Proceedings of the National Academy of Sciences, 1991
- DNA polymorphisms amplified by arbitrary primers are useful as genetic markersNucleic Acids Research, 1990
- Fingerprinting genomes using PCR with arbitrary primersNucleic Acids Research, 1990