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The transition time τ for the formation of salt layers was determined at different compositions of the electrolyte and current densities i.
The absorbance of the aqueous layers was determined at 410 nm against a control reaction blank (no enzyme included).
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Three target soil layers were determined at 0 5, 10 15, and 30 35 cm depth, based on the wetting fronts recorded during the experiment.
The absorbance of the toluene layer was determined at 520 nm.
The absorbance of the toluene layer was determined at 532 nm using spectrophotometer (Shimadzu UV-1600, Japan).
Concentration of OS extract in both layers was determined by UV vis spectrophotometry at 286 nm.
The repeat distance (membrane plus interlamellar water layer thickness) within the multilayer stacks was determined at different temperatures.
For the longitudinal images acquired over tested segments, the amount of echogenic bands/densities was determined at three separate layers: dermal, subcutaneous, and perimuscular zones (see Figure 3).
Poly allylamine hydrochrloride)–AlexaFluor 594 (PAH-AF594) and bovine serum albumin AlexaFluor 488 (BSA-AF488) were complementarily coated, and the fluorescent intensity for each dye was determined at each coating layer.
Subsequently, the crystal structure of the entire O-layer (also termed the outer membrane complex) was determined at a resolution of 2.6 Å (Fig. 1G) (Chandran et al., 2009).
Meanwhile, the corresponding network structure is confirmed which means the node numbers of input layers and hidden layers are determined.
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