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An on-line sampling system was designed for the 16 PAHs, which consisted of a glass wool filter, condenser, glass fiber filter, Teflon filter, and a Tenax trap.
After filtration through a glass wool filter, the samples were placed in NMR tubes for analysis.
After condensation of the liquid product, the gas passed through a glass wool filter before being collected in a gas sampling Teflon bag.
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Salivary glands were dissected from mosquitoes (day 16 20 post-bloodmeal), crushed using pestle and then glass wool filtered to obtain sporozoites used in subsequent assays.
After washes, the cells were finally harvested on glass wool filters with a suction-water-wash apparatus, dried, and counted in a beta scintillation counter [57].
Glass wool filters were transported on ice to the laboratory within 48 hr of collection.
Viruses were concentrated by trained staff using glass wool filters attached to taps (Lambertini et al. 2008).
The samples were filtrated through a freshly prepared glass wool-filter and the solvent was removed through evaporation.
After condensation of the liquid product, the gas passed through a glass-wool filter before being collected in a gas-sampling bag.
Within 24 hr the sediment samples were filtered through acid-washed glass wool and vacuum-filtered through 0.8 μm cellulose nitrate membranes (Whatman, Maidstone, UK).
The slurry was filtered through glass wool on top of Whatman #1 filter paper under vacuum to capture the remaining residue on the glass wool.
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