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.
© 2017 A. Soto, published by Johann Heinrich von Thünen Institute
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