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The fractions were used for the reactions, as described earlier.
These size fractions were used to target giant viruses (giruses).
For most patients, both CD8+ and CD4+-enriched fractions were used in the analysis.
Peripheral blood mononuclear cell (PBMC) negative fractions were used for germline DNA.
The mixture fractions were used to describe the thermochemistry.
In parallel, the same eukaryotic and prokaryotic-enriched fractions were used to produce metatranscriptomes by converting extracted RNA into cDNA.
The calculated footprint fractions were used to simulate the latter flux from the other two systems.
CO2 mole fractions were used to infer seasonal changes in airflow.
These fractions were used for hot-phenol RNA extraction or TCA protein precipitation and analyzed by northern blot or western blot, respectively.
The same fractions from a CsCl gradient of uninfected LLC-MK2 cells corresponding to the tested TV-containing fractions were used as negative controls.
Pellets were dissolved in 20 µl nuclease-free water (Ambion) and equal volumes from the fractions were used for quantitative PCR.
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