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. 2003 May 1;100(10):6263–6268. doi: 10.1073/pnas.0937399100

Figure 2.

Figure 2

(A) RT-PCR experiment using T. monococcum G3116 (winter growth habit) and AP1-, AGLG1-, and actin-specific primers. The PCRs for the three genes were performed by using the same cDNA samples. Lanes 1–5 indicate leaves. Lane 1, before vernalization; lanes 2–4, 2, 4, and 6 weeks of vernalization, respectively; lane 5, 2 weeks after vernalized plants were returned to the greenhouse; lane 6, unvernalized apices; lane 7, 6-week vernalized apices; and lane 8, young spikes. (B) AP1 transcription levels in leaves relative to actin measured by quantitative PCR. Lanes 1–5, leaves from plants at the same vernalization stage as samples 1–5 in A. Units are values linearized by using the Inline graphic) method, where CT is the threshold cycle.