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Analysing data of poly(propylene glycol) with Mw = 1000 (PPG 1000) we find the fastest process to show Arrhenius behaviour.
Of all the TLR-L testedataata of Poly(I C), R848, LPS, PGN, and flagellin not shown), only R848 was able to enhance the uptake of HS-induced apoptotic leukemic cells significantly.
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Besides, it also shows that the erase time to achieve the memory window of 3 V is around 5 ms at -13 V, which is very desirable as compared with the recently reported data of poly-Si NW based SONOS memory cells [9, 17, 18].
To validate microarray data, 50 ng of poly(A)+ RNA was reverse transcribed using M-MLV reverse transcriptase enzyme (Promega, Wisconsin, USA) in the presence of the ribonuclease inhibitor RNAsin (2 U/μL) (Promega).
Experimental data available for solutions of poly(4,4′-diphenylether-1,3,4-oxadiazole)s, POD-DPE, in sulfuric acid are used to illustrate this point.
The important results from the substantial body of experimental data on the formation of poly(1,4-phenylene sulfide) by polymerization of copper(I) 4-bromobenzenethiolate (CBT) have been documented.
These data indicate that augmentation of poly(I C -induced cytokI C -induced during mecytokine ventilation occuresponserily via a Myduringpendent pathway.
The difference between maternal exposure and our own data on actual concentrations of poly cyclic aromatic hydrocarbons (PAHs) in the human male fetal liver (Fowler et al. 2008) was striking.
ELISA data further confirmed that transfection of poly(I C) induced the production of IFN- β in a time-dependent manner.
Cyclability data of new "tailor made" poly N- oxyalkyl pyrrole electrodes both iN- oxyalkyl pyrroleelectrodesand in solid-state cells with (PEOSEO)20LiClO4 (a new polymer electrolyte conceived for room temperature applications) are reported.
Literature data on the viscosity of solutions of poly(butyl methacrylate) (PBMA) and poly methyl methacrylate) (PMMA) in diethyl phthalate (DEP) for different temperatures, including the range around and below Tg, the glass transition temperatures of the pure polymers, were evaluated by means of an approach that uses surface fractions as composition variables.
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