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The samples collected were extracted and analyzed by chiral HPLC.
The supernatants collected were extracted with dichloromethane with an equal volume of supernatant; this was repeated three times with fresh lots of dichloromethane.
The samples collected were extracted with three volumes of ethyl acetate by vertex mixing for 1 min and the organic phase was collected.
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The size-fractionated particulate that was collected was extracted and analyzed chemically for selected toxic/carcinogenic tobacco-specific nitrosamines (TSNAs), polycyclic aromatic hydrocarbons (PAHs), and other selected semivolatile organic compounds (SVOCs).
The collected samples were extracted with 2 ml DCM and reconstituted in 5 ml mobile phase.
The collected samples were extracted with 0.2 ml dichloromethane, evaporated by nitrogen stream, and reconstituted in 100 μl mobile phase.
The newly collected samples were extracted with 2 mL DCM and reconstituted in 5 mL mobile phase.
Potential input trees from the collected literature were extracted manually and compiled into a dataset of hymenopteran phylogenies.
Cells (1 × 10) were collected and lysates were extracted with 200 μl of extraction buffer following the manufacture's protocol.
Media and cells were collected and lipids were extracted.
Samples collected in 2008 were extracted and amplified as before, except without fluorescent-tagged ITS primers and sequenced as above.
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