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[Critical study of methods of estimation by an enzymatic method of serum triglycerides (author's transl)].

The authors describe a critical study of two entirely enzymatic methods of determination of serum triglycerides which differ mainly by the choice of hydrolytic agents: esterase and hydrolase by the Roche methods, lipase and esterase in the case of the Boehringer method. The estimation of the resulting free glycerol requires 3 sequential enzymatic reactions (glycerol kinase, pyruvate kinase, lactate dehydrogenase, ending by the measurement of the consumed reduced NAD. The study of the kinetics of the analysis in two stages is carried out using standard solutions of glycerol and with human sera of variable concentration; the optimal conditions of the reaction time and temperature are drawn up. The trials of repeatability and reproducibility from day to day were carried out together with evaluation of the precision. The method was compared with Beohringer's method (n = 50) using hydrolysis of alcoholic potash. The authors conclude on the use of the methods studied.

Esterases

Combined gel filtration, biuret/copper method compared with an immunochemical method for urinary protein measurement.

We compared an immunochemical method specific for plasma proteins with a chemical method, in which interfering substances are separated by gel filtration and "total" urinary protein is determined by the biuret reaction followed by reaction of protein-bound copper with diethyldithiocarbamate after a second gel filtration to remove nonprotein-bound copper. More than 250 24-h urine samples were analyzed by each method. There was linear agreement and a correlation of 0.96 between the two methods, but urinary protein values determined by the immunochemical method, especially for patients with multiple myeloma, were lower than by the chemical method.

Chromatography, Gel

Comparative study on two methods for serotyping of Staphylococcus aureus: the Pillet method and the Oeding method. II.-Possible identity between Pillet's antigen 9 and Oeding's antigen h1.

Using two techniques (agglutination and immunoprecipitation), the authors have observed that: -Pillet's strain CK9 and Oeding's strains 670 and 17A are very similar; -antigen 9 is also present in the three strains; the same relation is found in wild strains. Using agglutination and immunoprecipitation, there is a cross reactivity between h1 factor serum, serum 9 and strains CK9, 670 and 17A. A precipitation line involving strain CK9 and serum CK9 is described in the Pillet system. Finally, there is a strong presumption that Oeding's h1 antigen and Pillet's antigen 9 are identical.

Antigens, Bacterial