Ratios of different competing ligands were calculated for assays performed together on one assay plate.
It is difficult to give a definite explanation for mechanism of antioxidant of Eichhornia purified compound dependent on one assay.
One assay is based on the detection of DNA on agarose gels using highly sensitive SYBR Gold nucleic acid staining.
In one assay, the enzyme glucose oxidase was immobilized on the aminocellulose surface.
For example, one assay (White and Haber, 1990) is based on the inability of many restriction enzymes to cleave ssDNA.
One assay for enriched and characterized stem cells is based on the sphere-generated cells growing in serum free suspension.
Horizontal sections (10 μm thick) used for one assay were prepared from the same tissues and mounted on glass slides.
One assay was used to analyze EGFR homodimerization and EGFR phosphorylation on tyrosine residues.
Currently, two million compounds in PubChem have been tested in at least one assay, with 48% of them (0.96 million compounds) declared active in at least one assay.
A particular cut off may give 20% actives in one assay, but 100% actives in another.
Compounds were excluded if they were not active at least in one assay.
