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Each biological sample was analyzed with three technical replicates.
(b) For biological reproducibility, eight tissue samples for controls and three tissue samples for each NFPA subtype were used; and for technique reproducibility, each biological sample was analyzed with 2DGE for 3 5 times.
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To examine the capability of the method, real biological samples were analyzed.
Three independent biological samples were analyzed in each experiment.
Three independent biological samples were analyzed (n = 3); for each of them, data from two 10-fold dilutions of DNA matrix, each repeated in triplicates, were averaged.
Three independent biological samples were analyzed for each treatment.
Three independent replicates, prepared from independent biological samples, were analyzed.
Five biological samples were analyzed independently with each selected gene run in triplicate.
All biological samples were analyzed qualitatively and quantitatively according to established microbiological diagnostic criteria [ 16].
Three independent biological samples were analyzed for wild type and mutant genotypes.
Two independent biological samples were analyzed in triplicate for each probe.
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