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In transient transactivation assay, several compounds activated PPARγ and δ with little activity of PPARα.
In the clotting assay, several IgG preparations showed neutralising activity in a dose-dependent manner.
For the serial dilution assay, several doses for each DNA-damaging agent were employed and only one representative dose is presented.
This chapter describes the proper design of a fluctuation assay, several of the methods used to calculate mutation rates, and ways to evaluate the results statistically.
It is indeed often necessary to assay several amiRNAs, the sequences of which are based on computational predictions, to find one which effectively triggers knock down of a target gene (Warthmann et al. 2008).
To create the first series in the benchmark, the first assay in the dataset was selected and an attempt was made to find a set of 5 molecules whose activities differ by at least 0.38 log units (this attempt involved iterating randomly over all possible selections of 5 molecules from the assay several thousand times).
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In aerobic cytotoxicity assays several prodrugs exhibit diminished cytotoxicity.
From these assays, several synthetic madindoline analogues were identified as highly promising candidates for further development.
Due to improved analytical performance of the newest generation of troponin assays, several patients have mild elevations of this parameter.
For antimicrobial assays, several microorganisms including Gram positive bacterium S. aureus (ATCC 25923), Gram-negative bacteria E. coli (ATCC 25922), B. subtilis (ATCC 6633), and fungus C. albicans (ATCC 20032) were obtained from Kunming Medical College.
To bridge the gap between in vivo and in vitro angiogenesis assays, several microfluidic methods have been developed to generate in vitro assays that incorporate blood vessel models with physiologically relevant three-dimensional (3D) lumen structures.
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