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Before use, this batch was analyzed for cortisol content, which was found to be below the detection limits.
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A duplicate sample was analyzed for every five samples in a batch to evaluate analysis precision.
For the first batch, assembled contigs were analyzed for variations in individual EST sequences at single bases.
Three biological replicates with independent batches of 4a3B cells were analyzed for the diluent controls and treatments.
If antinutritional factors are indicated in future research, then each batch used in aquafeeds should be analyzed for antinutritional factors.
Multiple lab blanks were analyzed for each batch to check for laboratory contamination.
Blank samples containing matrix and reference samples were analyzed for each batch of samples with successful results.
From each farm, caecal samples from ten birds per house or compartment from one (Farm A) or two (Farm B) batches of broilers sent for slaughter preceding the intervention and two batches of broilers following the intervention were analyzed for the presence of VRE as previously described (Table 1) [ 2, 3].
High pressure carbonation of the subcritical water-biomass mixtures were conducted in a small batch reactor and the resultant hydrolyzate mixtures were analyzed for sugar content using SEC and HPLC-RI detection.
Transiently transfected HepG2 cells from the same batch of transfection as in Figure 7C were analyzed for total or cell surface NTCP expression at 24 hr post-transfection as described in Figure 7B.
To observe the effect of matrix on analyte quantification, six samples from different plasma batches prepared at LQC and HQC level, were analyzed for % accuracy and precision (%CV).
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