Figure 2. Gel picture showing the PCR
amplified product (350 bp) of the three isolates of Aspergillus
flavus. Internal transcribed spacer 2 was used as a target region
for DNA amplification. The lane L1 was loaded with 100 bp DNA Ladder;
the lanes L2, L3, L4, L5 were loaded with 10 μl of the amplified
product from the test strains C1, C2, E1, E2, respectively, in 1.5%
agarose gels. Lane L6 was loaded with a negative control to rule out
false-positive results.