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Binding was measured by incubating AtraPBP1 with test ligands, separating unbound and bound protein, extracting pheromone from the latter sample, and analyzing by gas chromatography, according to a previously reported protocol [5].
Amplification efficiencies, analytical sensitivity, and accuracy of gene assays were measured by serially diluting an RNA sample and analyzing features of the linear regression between RNA expression measured by the crossing point (Cp) versus the log2 of the RNA input per PCR assay well.
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Each third was selected at least two times per sample and analyzed.
Therefore, different amounts of methyldopa were spiked to the sample and analyzed by the proposed method.
We characterize the connectivity of the ports in our sample and analyze the results.
Dye sensitized solar cell was fabricated using the nanocomposite film for this sample and analyzed.
The PE positive cells were eluted from the column (post-enrichment sample) and analyzed by FACS.
Approximately 20,000 cells were collected per sample and analyzed using western analysis.
Take a blood sample and analyze it.
DB, EK, and LDR sample and analyzed the synovial tissues.
SW generated the microarray sample and analyzed the transcript data.
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