Sentence examples for assays were selected for from inspiring English sources

However, MLP assays were selected for scientific merit and therefore tend to be non-redundant.

In addition, rodent and amphibian in vivo assays were selected for the proposed battery based on their capacity to detect direct and indirect effects on thyroid function (hypothalamic-pituitary-thyroidal, HPT, feedback).

Based on these criteria, the following candidate markers with available serum assays were selected for testing: WFDC2, MSLN, IGF2, CHI3L1, MMP7, BMP7, LCN2, TACSTD1.

Using this strategy, the following candidate markers with commercially available ELISAs or other published assays were selected for testing: MSLN, WFDC2, IGF2, CHI3L1, MMP7, BMP7, LCN2, TACSTD1.

The inventoried TaqMan gene expression assays were selected for the detection of rat RNA transcripts (Applied Biosystems, Foster, CA, USA).

Twenty-seven GBS assays were selected for independent validation, and the observed accuracy was 95.9% (see the section Materials and Methods).

CTL clones demonstrating rapid in vitro growth and specific lysis of antigen-positive tumor targets in a Cr51 release assay were selected for expansion.

A total of eight intragenic sites identified in the ChIP-chip assay were selected for functional analysis.

The organisms found to be positive for above chromogenic assay were selected for further process optimization for the production of 3-substituted catechol at pilot scale.

Fifty-five AML patient samples with LC50 values for ara-C, cladribine, decitabine, fludarabine and gemcitabine (determined with the MTT assay) were selected for RNA isolation.

Five aEPEC strains representing each adherence pattern on HEp-2 cells (LAL, LA, AA, DA, and UND) and one nonadherent (NA) strain, each of them showing the highest levels of biofilm formation by the CV assay, were selected for the CFU assay on polystyrene and prefixed HEp-2 cell surfaces.