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cDNA library clones were PCR amplified, and those showing a single band were selected for sequencing.
cDNA library clones (1100 clones) were PCR amplified, and those showing a single band were selected for sequencing.
1100 cDNA library clones were PCR amplified and the ones showing single band were selected for sequencing.
Finally, eighty four artifact-free epochs from middle data segment of each emotional state across delta, theta, alpha, and beta frequency band were selected for further analysis.
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Nine equal-power spectral bands were selected for the pyrometers from wavelengths between 8 and 14 μm.
Thirteen Hyperion bands were selected for analysis based on the documented and hypothesized importance of various spectral wavelengths to forest characterization.
The bands were selected for the analysis of polyethylene and carbon nanotube in the 450 4,000 cm−1 range.
Bands were selected for quantification using the automated volume contour tool.
These bands were selected for protein identification.
PCR products were visualized in a 2% agarose gel, and singleton bands were selected for sequencing.
Five hundred and ten primer that pairs amplified clear and strong bands were selected for labeling with fluorescent dyes.
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