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RNA samples from 10 individual plants were pooled for microarray analysis.
Fractions 7 10, consisting of mRNA with four or more bound ribosomes, designated "heavy", were pooled for microarray analysis.
Total RNA from up to 10 thymi were pooled for microarray analysis and quantitative PCR.
Each sample from the control (n = 7) or HF (n = 7) offspring were pooled for microarray analysis (two-class experiment [ 48]).
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RNA from two rats of the same age and time point was pooled for each microarray sample.
RNA from the equivalent of 100,000 unc-4 GFP unc-4 GFPs pooled for each separate microarray experimeneurons
Following a post-processing step, 7 μg of labeled DNA for each reference and test sample were pooled for hybridization onto microarrays as previously described [ 15].
Two biological replications were conducted and the leaf samples from corresponding time points were pooled for ROS analysis and microarray experiments.
Equal amounts of RNA from each replicate culture were pooled for each strain and used for microarray labeling and hybridization, qPCR and the nCounter analysis.
A part of each RNA preparation was used to prepare RNA pools for microarray analysis.
A part of the isolated RNA was used to prepare RNA pools for microarray analysis.
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