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The LacZ expression in each strain was determined by filter assays.
The range of the pixels to be used is determined by filter window size N × N.
This procedure revealed a ∼10-fold JAM-A concentration as determined by filter centrifugation of dilutions of recombinant JAM-A in complete medium.
The amount of P in each fraction was determined by filter binding and exposure to a phosphorscreen.
k-means clustering of units with two clusters resulted in well separated populations (indicated by dotted line, [ Figure 3 figure supplement 1F]), albeit indicating a high correlation between these two features (arising possibly due to the spike waveforms being narrower than measured, which in turn is determined by filter settings).
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The dry weight of microalgal cells was determined by filtering the culture through 0.45-μm pore-size membrane filters.
Dry biomass data were determined by filtering 1 ml of cell suspension through preweighted Whatman membrane filters (pore diameter of 0.2 μm).
Dry weight was determined by filtering the biomass through normal filter paper and the cell clumps were removed from the immobilization materials to obtain the fresh weights of biomass for each flask.
Faecal coliform was determined by filtering 60 ml of sample through a 0.45 um filter onto a Petri dish containing MFC and incubated at 44 ± 2 °C for 18 24 h and colonies were then counted.
Composition of each library was determined by filtering all decoded reads to human genome.
The drug content was determined by filtering the solution through 0.4 μm membrane.
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