|
Figure 2.
|
-
Amplification of
the plastid gene psaA from Taipei 309 seedlings using different
concentrations of MgCl2. 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, all at
45°C.
-
The annealing temperature
was raised to 50°C to remove the extra bands.
-
Amplification of
psaA from Taipei 309 seedlings and cells. Lane 1, DNA sample from
Taipei 309 seedlings, lanes 2-4 DNA samples from 1-, 2- and 3-week-old
cells.
|