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A simple chemiluminescence assay for the determination of reactive oxygen species produced by human neutrophils.
Application of the flow cell to the determination of reactive phosphorus in estuarine waters with wide variation in salinity and refractive index is also described.
The information inferred from NQR study on local electron density distribution together with analysis of charge distribution, provides excellent means for determination of reactive sites and hence, can indicate possible promising directions to be followed in drugs design.
New algorithms for the computation of the simultaneous chemical and physical equilibrium involved in simulations of reactive flash operations, calculations of phase diagrams, and the determination of reactive azeotropes are presented.
Iron (Fe) redox cycling and sorption/complexation reactions influence numerous soil biogeochemical processes, and the precise, rapid, and low-cost determination of reactive Fe pools is critical for understanding these dynamics.
The determination of Reactive Oxygen Species (ROS), ferric reducing ability of plasma (FRAP) and carbonyl residues (CO) in the plasma, was carried out as previously described [ 9].
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Determination of the reactive zone and removal of lesions within the reactive zone are important for curative treatment.
After determination of the reactive forces, certain features were attributed to the plate's edges.
The latter was clearly demonstrated by the affinity determination of the reactive quinoneimine of the BIRB796 inhibitor.
Fluorescent probes of 2′,7′-dichlorofluorescein diacetate (DCFH-DA) were employed in the determination of intracellular reactive species formation in hippocampal cells.
Determination of hepatic reactive oxygen species (ROS) was followed by the conversion of 2′,7′-dichlorofluorescein diacetate (H2DCFDA) to fluorescent 2′,7′-dichlorofluorescein (DCF).
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