About this article
Published Online: Oct 27, 2017
Page range: 139 - 140
Received: Aug 11, 2004
DOI: https://doi.org/10.1515/sg-2004-0025
Keywords
© 2017
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.
Combined use of two newly designed PCR primers with already described rpl2 and trnH primers, yields amplification of three non-independent products from the hypervariable JLA region of eucalypt chloroplast. Polymorphism analysis of the resulting PCR markers is proved to be a time- and cost-efficient alternative to traditional cpDNA techniques as RFLP or sequencing for Eucalyptus globulus Labill. population genetics studies.