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In contrast, both cell cycle markers were unchanged in cotyledons of ΔYDA plants, where only rare cell divisions take place (Figure 8C).
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De Oliveira et al. (1994) reported that there were reductions in chlorophyll a and b in cotyledons of Glycine max cv Bessier and Doko as Cd concentrations increased.
In cotyledons of Scadoxus membranaceus (tropical grass), vacuoles occupied ∼25%% of cell cross-sectional area.
Testing STM and AS1 (and AS2, not shown) in pools of cotyledons separated from the rest of the body, showed STM expression in cotyledons of SAM-less seedlings but not in those of controls (Fig. 4b).
In soybean, GmFLD is highly expressed in expanded cotyledons of seedlings, roots, and young pods.
Since soybean 7S promoter also has high activity in seed cotyledon of soybean, we checked the JcFAD2-1 transcript level in the cotyledons of T1 transgenic Jatropha.
The seed kernels were then open in two cotyledons of about 9.7 ± 2.4 mm thickness for drying.
Metcalfe and Chalk (1950) mentioned the secretory cells found in the cotyledons of many genera including Evolvulus, but did not specify the type of cell.
However, the GUS intensity was stronger in cotyledons, vascular tissues of primary root and inflorescences than other organs (Figure 8).
In cotyledon tissue of SAM-less rpk1-7 seedlings, we detected ectopic expression of the SAM-related STM, KNAT1 and KNAT2 genes together with cotyledon specific expression of AS1.
Noticeable changes in mass occurred in cotyledons with the progress of seed maturation.
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