Flow cytometry enabled the quantitative assay of delivery into the cells.
The quantitative assay of platelet activation was determined by measuring the production of soluble P-selectin.
It was later proved by the quantitative assay of arsenite oxidation in case of isolated Brevibacillus sp. A1a.
The quantitative assay of the antimicrobial activity was performed by liquid medium microdilution method in 96 multi-well plates.
The proposed biosensing-device also demonstrated high stability and reproducibility, which was able to offer great promise for the quantitative assay of K562 in routine analyses.
Quantitative assay of l-2-hydroxyglutaric acid (l-2-HGA) is important for the diagnosis of l-2-hydroxyglutaric aciduria.
The proposed approaches were validated and successfully applied for the quantitative assay of a small concentration of ADP in its pharmaceutical gel.
The results may be of interest to develop a specific analytical procedure with advanced specificity for quantitative assay of capsaicin and dihydrocapsaicin in pharmaceutical products and in foods.
The quantitative assay of the minimal inhibitory concentration (MIC; μg/mL) was based on liquid medium twofold microdilutions performed in 96-multi-well plates.
Hydrogel glycan microchips were used for quantitative assay of antibodies against blood group antigens and assay of lectins with fluorescent detection.
