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The resulting DNA is highly contaminated with high level of secondary mateials, such as high levels of polysaccharides, polyphenols and other unknown sticky compounds that bind or co-precipitate with DNA and form a viscous complex. It is not possible to laod such DNA samples into the electrophoresis well.

You could try the 3% CTAB DNA extracion protocol, modified from Zeng et al. 2002, ACta Botanica Sinica 44; 694-697.

1. washing out polysaccharides with CTAB-free buffer from homogenate.
2. increasing the percentage of CTAB in extraction medium.
3. using high concentration salts pior to DNA precipitation with isopanol.
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