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A glass microfiber filter was used as separator.
Accordingly, when there were no surface modification, DNA and YOYO-1 adsoreadilyadily on the glass microfiber filter paper, and prolonged the interaction between DNA and YOYO-1.
Aerosol scrubbing efficiency was measured based on the inlet and outlet aerosol concentrations of the scrubbing vessel with isokinetic sampling systems including a glass microfiber filter.
The synthesized materials were collected using a glass microfiber filter paper (Whatman) for further characterization.
The microporous polypropylene (Celgard 2400) and glass microfiber filter membranes (Whatman, Grade GF/A) were utilized as a separator of LIBs and SIBs, respectively.
This solution was then filtered through a 1 μm glass microfiber filter (Whatman GF/C, Sigma-Aldrich, St . Louis MO, USA) and kept refrigerated under N2 atmosphere, until subjected to preparative high-performance size exclusion chromatography (HPSEC).
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After fumigant removal, the fumigated soils (number of replicates N = 3) were extracted with 100 mL of 0.5M K2SO4 at room temperature with 30-min of shaking, and then filtered using pre-combusted glass microfiber filters (Whatman GF/F).
NM (20 μmol) or vehicle control was applied onto 6 mm glass microfiber filters affixed to the shaved dorsal skin of CD-1 mice for 6 min.
Following the 30 min of shaking, the samples were filtered through Whatman™ GF/F 70-mm glass microfiber filters using glass funnels.
Calibration of the turbidity meter was done by filtering some water samples through pre-weighed Whatman GF/F (0.45 μm pore-size) glass microfiber filters.
Dry biomass weight (g/L) was calculated by filtering 10 ml microalgae culture samples through pre-heated, pre-weighed glass microfiber filters (Whatman GF/C, 47 mm).
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