DNA Extraction Protocol for Plants with High Levels of Secondary Metabolites and Polysaccharides without Using Liquid Nitrogen and Phenol

<table>Agarose gel (1.5%) showing the PCR amplification of representative DNA samples. (Lane1 and Lane2: mangroves matK and rbcl gene respectively; Lane3 and Lane4: salt marsh’s matK and rbcl gene respectively; Lane5: Negative control; Lane6: 2 Kb DNA ladder).</table>

International Scholarly Research Notices

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Figure 4

Figure 4: DNA Extraction Protocol for Plants with High Levels of Secondary Metabolites and Polysaccharides without Using Liquid Nitrogen and Phenol 