Skip to main content
. 2001;1(1):38–44. doi: 10.1155/S1110724301000110

Figure 2.

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.