The use of agarose blocks containing embedded DNA improves the PCR amp
lification from templates naturally contaminated with polysaccharides
or humic acids, two powerful PCR inhibitors. Presumably, the differenc
e in size between the DNA macromolecules and these contaminants allows
their effective removal from the agarose blocks by diffusion during t
he washing steps, whereas genomic DNA remains trapped within them. In
addition, agarose-embedded DNA can be directly used for PCR since low
melting point agarose does not interfere with the reaction. This simpl
e and inexpensive method is also convenient for genomic DNAs extracted
by other procedures, and-it is potentially useful for samples contain
ing other kinds of soluble inhibitors, overcoming this important probl
em of current amplification techniques.