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By observing the effects of additives on the catalytic OCM activity of Na2WO4/SiO2 catalysts, the reducibility of metal additives, quantified by the standard reduction potentials, is observed to improve the methane conversion and olefin selectivity, indicating that the active sites of activating methane and dehydrogenating paraffin are identical.
Automatically derived RM activity concentrations were within 5%% of manually derived estimates, indicating that the active contour method can identify the intraosseous activity concentration in the LV sufficiently accurately.
This shows that coexistence of Au and TiO2 is needed to obtain high catalytic activity in the WGS reaction, indicating that the active sites are either on the Au TiO2 interface or that the reaction follows a bifunctional mechanism.
The blocking probability increases with the time interval more significantly during low traffic times, indicating that the active PBSs set should change frequently in these times.
Pyridine-type nitrogen has been found by XPS after heat treatment at both temperatures, indicating that the active sites are already formed at 550 °C.
Results: A significant time by group interaction effect was found in the measure of spatial ability (i.e., block design test) indicating that the active group's performance declined significantly at week 4, compared to placebo group (F 4,64)=3.78, P<0.01).
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Thiol reagents (L-cysteine and dithiothreithol) strongly protect the enzyme from the loss of enzymatic activity, while boric acid and fluoride show weaker protection, indicating that the active-site sulfhydryl group of JBU was potentially involved in the blocking process.
Furthermore, in vivo Förster resonance energy transfer (FRET) experiments indicated that the active form of Pit induces the activation of OsRac1 at the plasma membrane.
A structure activity relationship study indicated that the active core of DH is the C-terminal hepta-peptide, LWFGPRLa.
The higher activity of Fraction C indicated that the active components might be more soluble in methylene chloride than what was previously reported [ 15, 20].
Conversely, the recent report of anti-parasitic activity of indomethacin derivatives [41] indicates that the active sites of parasite enzymes, if not their primary sequences, are sufficiently homologous to their mammalian counterparts.
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