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Experiments demonstrate that in the highly alkaline environment of cement, Mg2+ precipitates as voluminous Mg(OH 2 which entraps significant amounts of the graft copolymer.
The gas-sensing experiments demonstrate that, in contrast with singular ZnO nanoparticles, the ZnO nanocages show significantly enhanced chemical sensing sensitivity and selectivity towards low-concentration volatile organic compounds, typically, acetone and benzene.
Laboratory experiments demonstrate that in situ recovery of pooled tetrachloroethene (PCE) from porous media may be accomplished more efficiently using multiple-step alcohol floods than with single alcohol floods.
For example, common garden experiments demonstrate that in most species both plastic and genetic factors are important for determining how photosynthetic efficiency, leaf area, and leaf mass per area respond to altitude [1] [5].
These experiments demonstrate that in vivo drug-sensitivity assays are not dependent on the injection of mice with high numbers of sporozoites, which requires time-consuming manual dissection from mosquito salivary glands.
These experiments demonstrate that, in addition of being low activators, the Brucella molecules that putatively bear PAMPs (Table 1) do not inhibit the generation of TNF-α in vivo or in vitro.
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Taken together, these experiments demonstrate that PsAvr3c physically interacts with GmSKRP1/2 in vitro and in vivo.
Further experiments demonstrated that in addition to catalyzing the CNT growth, catalyst particles can also decompose/etch the C sp2/sp3 bonds including those in the CNTs.
Validation of the simulation results with the experiments demonstrates that, in general, simulation satisfactorily reproduces the key fluidization and mixing features of biomass particles such as the global and local time-average distribution and velocity profiles.
Comparing the simulated response of the RVEs with the experiments demonstrates that in the small strain regime the stress is under-predicted since the polymer matrix is modeled by using only one single relaxation time.
Coimmunoprecipitation experiments demonstrated that, in the same way, TRIM25 interacted with the helicase domain of RIG-I as efficiently as CARD domain of RIG-I.
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