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. 2017 Nov 3;9(4):290–293. doi: 10.1016/j.jaim.2017.10.001

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© 2017 Transdisciplinary University, Bangalore and World Ayurveda Foundation. Publishing Services by Elsevier B.V.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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Fig. 1 — PCR amplification of genomic DNA with species-specific markers. (A) Markers GAR-F and GAR-R gave a 142-base amplicon with Gmelina arborea samples (Lanes 1–3); Lanes 4 to 6 – G. asiatica; Lanes 7 to 9 – M. nudiflores. (B) GAS-F and GAS-R markers gave a 93-base amplicon with only G. asiatica samples (Lanes 1–3); Lanes 4 to 6 – G.arborea; Lanes 7 to 9 – M. nudiflores. (C) Markers TNF-F and TNF-R gave 150-base amplicon with only M. nudiflorus samples (Lanes 1–3); Lanes 4 to 6 – G. arborea; Lanes 7 to 9 – G. asiatica. Lane M, 100 bp DNA ladder.