Sentence examples for nitrate nox from inspiring English sources
Nitrite and nitrate (NOx) levels were assessed by a modified Griess method.
Fluid was serially harvested from the wound compartment at days 2, 4, 7, 9, 11, and 14 for nitrite/ nitrate (NOx) analysis.
TNF-α determinations, IL-6, IL-10 and nitrite / nitrate (NOx) routine employed as a surrogate marker of NO metabolism in mouse plasma by ELISA (commercially available kits) ratio were performed.
Advanced oxidation protein products (AOPP), thiobarbituric acid-reactive substances (TBARS), total thiol content (T-SH) and nitrite and nitrate (NOx) levels were assessed in plasma while the levels of interleukin-1 beta (IL-1β), interleukin-6 (IL-6), interleukin-10 (IL-10), tumor necrosis factor alpha (TNF-α) and interferon-gamma (IFN-γ) were evaluated in the serum.
Levels of eotaxin (ET -1, total nitric oxidET -1total + nitrice, Noxideinitritelular adhesion molecule-1 (ICAM-1), and monocyte chemoattractant protein-1 (MCP-1) in the serum was assayed for evaluating myocardium function using commercial kits (R&D Systems, Minneapolis, MN).
Nitrite and nitrate (NOx) levels in plasma were measured by fluorometry.
Nitrite and nitrate (NOx-) and 3-nitrotyrosine (3NT) in plasma and bronchoalveolar lavage fluid (BALF) were analyzed by the Griess/vanadium chloride method and ELISA, respectively.
Among ascitic patients, those with high LBP showed greater (P <.05) levels of sCD14, tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), nitrites + nitrates (NOx)/creatinine, and renin, and lower vascular resistance.
Nitrites and nitrates (NOx) were measured using the Griess Reagent and the resultant purple azo derivative was measured spectrophotometrically at an absorbance of 540 nm [ 14].
Specific laboratory tests included serum fibrinogen and plasma NO expressed as its metabolites, nitrites and nitrates (NOx), as measured by the Griess reaction.
To determine reference values for serum nitric oxide metabolites (nitrite + nitrate = NOx) concentrations in adult subjects.
