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Figure 1.
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PCR amplification
of the 5' end of the mitochondrial gene coxII using total DNA
from Taipei 309 seedlings as substrate. Different concentrations
of MgCl2 were used to optimise the PCR conditions. Lane 1, DNA
marker, lane 2, 0.5 mM MgCl2, lane 3, 1 mM MgCl2, lane 4, 1.5
mM MgCl2 and lane 5, 2 mM MgCl2.
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PCR amplification
of the 5' end of coxII under optimal conditions. Lane 1, DNA
sample from Taipei 309 seedlings, lanes 2-4 DNA samples from
1-, 2- and 3-week-old cells.
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