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. 2011 Oct 11;6(1):39–46. doi: 10.1007/s11816-011-0193-0

Fig. 3.

Fig. 3

Analysis of the LL-37 gene expression in the transgenic homozygous lines by using reverse transcription polymerase chain reaction. Total RNA was isolated from each plant, and 0.5 μg of this RNA was amplified with LL-37-specific primers. The Chinese cabbage actin gene was amplified as a loading control. The amplification products of the LL-37 gene were separated using a 1.5% agarose gel. Lanes: M DNA ladder, WT wild-type plant, B21–B24 independent transgenic homozygous lines