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Furthermore, the oxidation reactivity of different substrates was in the following order: DBT > 4,6-DMDBT > BT.
TEM observation revealed that the ZSM-5 deposited on these carbon substrates was in the form of nanoparticles with 10 20 nm of diameters.
Biofilm biomass on the substrates was in the following sequence: coarse sand > pebbles > glass beads (4.8 × 107, 4.5 × 107 and 3.5 × 105 CFU/cm2), which was confirmed by CLSM.
The formation of multilayers on Ni/Gra substrates was in evidence since the thickness of different aryl layers varied from few to 30 nm depending on the modification procedures as well as the diazonium compounds used and the XPS analysis revealed a peak at about 400 eV for all aryl-modified Ni/Gra samples suggesting the multilayer formation also through azo linkages.
The activity of TH2-CP toward the substrates was in order of Phe-Phe>Phe-Arg>Phe-Ser>Phe-Ala>Phe-Gly, Leu-His>Leu-Pro = Leu-Asp = 0 U/mg, Lys-Phe>Lys-Leu, Arg-Phe>Arg-Lys and Z-Gly-Leu>Z-Gly-Phe>Z-Gly-Glu = Z-Gly-His = 0 U/mg (Fig. 4).
The binding of the hairpin substrates was in general in good agreement with the incision efficiency (summarized in Fig. 4C).
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In this cell, films made on transparent substrates are in direct contact with liquid solution.
These substrates were in powder form; i.e., graphite (Cgr) and titanium (Ti).
Because the substrates are in competitive conditions, the preferences of particular caspases to given peptide sequences are most clearly demonstrated.
The carbons of different organic substrates are in the range of 9.05 % in vegetable compost to 37.34 % in rabbit dung.
The metal substrates were in all cases silver, ranging in composition from nearly pure silver to ninety-six percent silver.
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