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The second approach is to account for the resources adjustments effect by a separate filter.
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Let us therefore extend this model by including separate filters for the ON and OFF pathways.
The approach is to capture the effects of inputs from both ON and OFF bipolar cells to the ganglion cell by separate filters, one with typical OFF-type characteristics, the other a typical ON-type filter (Fig. 2).
The states of the pedestrians are estimated by separate filters.
These signal processing tasks are traditionally implemented by separate filters in the time domain, and we will show that they can also be implemented in the FB-transformed domain as independent intermediate processing elements (IPEs).
The cells were examined by an epifluorescence microscope (NIKON Eclipse) using separate filters for nuclei, DAPI filter (blue), and for QD (620); TRITC filter (red).
To distinguish between those two possibilities, CPJV501 and strain 13 pfoA-null mutant were inoculated into the same 100 mm tissue culture dish but physically separated by a Transwell filter.
The two chambers were separated by a policarbonate filter with pore size of 0.4 μm.
The two compartments were separated by a polycarbonate filter (12 μm pore size, Nucleopore, Costar, Cambridge, MA, USA) coated with 0.005% gelatine to allow cell adhesion.
The magnitude of the responses induced without contact (noted above) tended to be less than that shown in Figure 1 where cells were only separated by a porous filter.
Two-photon excitation was performed at 830 nm, and the fluorescence signals of the Ca2+ indicator fura-2 (Kd: ∼200 nM) and the polar tracer sulforhodamine B were separated by a dichroic filter and captured at 420 560 and 570 650 nm, respectively, and images were acquired every 1 sec.
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CEO of Professional Science Editing for Scientists @ prosciediting.com