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In order to enable statistical analysis three biological replicates were produced by in vitro fertilization from different pairs of male and female frogs.
Four independent biological replicates were produced from each time points.
Three independent biological replicates were produced for the protein abundance quantitation in 1-DE, 2-De, and shotgun analyses.
For each cell-type, three biological replicates were produced, based on distinct rounds of plant cultivation and root embedding.
After three biological replicates were produced for each time point and pooled, RNA was sequenced producing a total of ~40 million paired reads for each time point.
In brief, 8 biological replicates were produced for each sample-type, and each sample was analysed using Taqman array cards, 384 well microfluidic arrays produced by Applied Biosystems.
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For each species, only one biological replicate was produced for both the anterior and the posterior midgut.
Two technical replicates were produced for each biological replicate, for a total of eight hybridizations.
Two replicates were produced for each biological replicate, thus obtaining six gels per condition (n = 6).
For each tissue sample, three biological replicates were collected producing a total of 12 data points per probe (2 tissues × 2 genotypes × 3 replicates).
For each common bean tissue sample, three biological replicates were collected producing a total of 9 data points per probe (3 tissue types × 3 replicates).
More suggestions(16)
biological samples were produced
biological replicates were obtained
biological markers were produced
biological replicates were analysed
biological weapons were produced
biological replicates were grown
biological replicates were performed
biological replicates were conducted
biological dads were produced
biological agents were produced
biological replicates were normalized
biological replicates were set
biological replicates were done
biological outcomes were produced
biological replicates were measured
biological replicates were analyzed
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