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. 2009 Dec;10(12):870–876. doi: 10.1631/jzus.B0920204

Fig.3.

Fig.3

PCR analysis of T0 plants

Genomic DNA, isolated from the leaves, was screened for the integrity of the minimal gus reporter gene cassette by PCR using two primer pairs: 35S/NOS (2052 bp) and gusF1/gusR1 (1019 bp). M: DNA marker DL2000 (TaKaRa); Samples 1~12: transformed soybean plants (positive results are shown except in Sample 4 and Sample 9); C: the plants from the untreated flowers; P: pBI121. A similar PCR analysis was carried out in large-scale transformation with soybean plants from the flowers transformed with 0.1× SSC as the control