Figure 2.
Autoradiograph showing PCR amplification of genomic DNA from the low glycitein Forrest (F), the high glycitein parent (E) and the F5:13 selected RIL segregating for glycitein soybean seed content with the BARC-Sat251 primers. The labeled PCR products were electrophoresed on an 5% polyacrylamide denaturing gel (H: High content, L: Low content of glycitein seed content.