Combining the aforementioned findings, we conclude that the newly developed DNAsimp lysing buffer was efficient for DNA extraction from common tropical plants. Considering that no harmful and dangerous reagents were used in this method, it was a safe and friendly DNA extraction protocol. Furthermore, as reported by Mace et al. (2003), the clarified lysate can be purified on glass fiber plates for increased throughput or alternatively precipitated in 96-well plates following the original protocol which would broaden the range of potential applications of the newly developed DNAsimp lysing buffer. In conclusion, the method we introduced in this study might be an attractive approach for DNA extraction from common tropical plants.