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In our AT study, SNPs were successfully associated with GS concentration in seeds.
SNPs and GEMs were separately used for AT study on total GS concentration in seeds.
Seeds of 101 B. napus lines were harvested and measured for total GS concentration using NIRS (Fig. 1).
Furthermore, the tradeoff was evident among and within all populations, and we controlled for plant size in these analyses (Fig. 3); therefore, the tradeoff is not simply an artefact of GS concentration increasing as plant size decreases (Koricheva 1999).
The average GS concentration of haplotype I (56.3 µmol g−1) was only 55% of that of haplotype II (the wild type), consistent with the net 8-bp (frame-shift) deletion reducing the functional properties of the encoded protein.
This approach was used to construct a co-expression network for the GS concentration that contained 122 modules (co-expressed genes), with between 31 and 16,989 unigenes in each module.
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The trends also held for the total GS concentration because 2-hydroxy-1-methylethyl GS and total GS concentrations are highly genetically correlated (r = 0.98).
The relaxation rate increased linearly with increasing actual Gd concentration.
The thermoelectric properties of the composites were investigated as a function of the graphite (G) concentration.
The optimal parameters were: initial pH 4; [H2O2]0 = 2 mM; catalyst mass 0.01 g; concentration of dye 30 mg/L.
Monoglyceride (MG), beeswax (BW) and propolis wax (PW) have been used as structuring agents at 5 g/100 g concentration to gel pomegranate seed oil.
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