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In addition to quantification using the MachBiophotonics ImageJ 1.42I program, Her2/neu expression within the tumor samples was expressed as a histoscore (as described in the Methods).
For all the consensus sequences, the differential expression between treated and control samples was expressed as a ratio calculated with the Pfaffl equation [ 78].
The total content of phenols in samples was expressed in equivalents of GA (mg) in a gram of dried plant material.
Solubility of protein in surimi samples was expressed as the percentage of total protein in surimi gels solubilised directly in 0.5 M NaOH.
The isotope ratio of D/H and 18O/16O in the samples was expressed as per mille deviation relative to Vienna-Standard Mean Ocean Water (V-SMOW) as follows: delta ( {permille} ) = (R_{text{sample}} /R_{text{V - SMOW}} - 1); times 1000 (1 where R is the ratio of the heavy to light isotopes (18O/16O or D/H) in the sample or standard.
One g of different dried durian seed gum powder was suspended in 10 mL of distilled water, vortexed for 2 min and then centrifuged with a refrigerated centrifuge 3-18 K (Sartorius, Sigma 3 18, Göttingen, Germany) at 3000 g for 30 min. The free water was decanted and the water absorbed by the samples was expressed as grams of water absorbed per 100 g of seed gum.
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The agreement between qRT-PCR and microarrays in expression profiles across samples is expressed as Pearson correlation coefficient.
Enzyme activities of all the samples were expressed as U · l−1.
The results of samples were expressed as mg of rutin equivalents of total dried fractions.
The results of samples were expressed as mg of rutin equivalents of total extractable compounds.
Total phenolic contents of the samples were expressed in terms of Gallic acid equivalent (mg/L and or mg/g).
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