Sentence examples for ml were filtered from inspiring English sources

For APP, unstained subsamples (2 6 mL) were filtered through 0.2-μm polycarbonate membranes (MacIsaac and Stockner 1993).

Autotrophic nanoplankton and heterotrophic nanoplankton subsamples (10 17 mL) were filtered through 0.8-μm polycarbonate filters and counted after primulin staining (Caron 1983).

For the TSS analysis, well-mixed samples with a volume of 10 mL were filtered through weighed standard glass-fiber filters (Whatman GF/C, diameter 47 mm).

To determine the pigment composition, samples of cultures (30 mL) were filtered through GF/F filters (25 mm), immediately frozen in liquid nitrogen and stored at −80°C until further analysis.

Before the DLS analysis of the QDs, the colloidal solutions (3 mL) were filtered three times through a 0.45-μm aqueous syringe filter (Millex LCR 25 mm, Millipore, Billerica, MA, USA) to remove any possible dust.

50 ml were filtered through a TMMP Millipore 5 µm-pore size filter and then through a GTTP Millipore 0.2 µm-pore size filter in a field laboratory set for this purpose.

In short, a known amount of water (generally 500 ml) was filtered through a GF/F glass fiber filter immediately after collection.

A known volume of broth (5 mL) was filtered through a cellulose membrane (Merck ®) with a pore size of 0.22 μm previously dried to constant weight.

After incubation for 3, 6 or 15 days, the fermented product (100 ml) was filtered through the Whatman No. 1 filter paper and then extracted twice with ethyl acetate (50 ml).

Spores were eluted with 20 mL 0.1% (v/v) Tween-80, of which approximately 15 mL was filtered through lens paper, transferred to a sterilized 50-mL flat-top centrifuge tube, and then separated by centrifugation (2700×g, 5 min).

Another 60 mL was filtered and placed in a sample bottle without preservative for ion chromatography (IC) and total organic carbon (TOC) analysis (except for samples collected in May 2012).