Overexpression of the AtSHI Gene in Poinsettia, Euphorbia pulcherrima, Results in Compact Plants
Figure 4
Quantitative real-time PCR analysis of AtSHI transgene in different transgenic lines of poinsettia.
Two microgram total RNAs from transgenic poinsettia lines and the endogenous control, α-tubulin gene were used for synthesize cDNAs prior the real-time qPCR analysis. Values are means of three technical replications except TL2 (n = 2). Data were analyzed using the 2−△△CT method and represented as log10 values. Vertical bars represent the ± SE (standard error).