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Radioisotopes can be assayed using a radioanalytical method.
Genetic variation can be assayed using a variety of molecular markers, including structure variation (SV) markers such as insertions/deletions (InDels) and copy number variations (CNV).
Urine NGAL will be assayed using a human-specific commercially available enzyme-linked immunosorbent assay (ELISA, AntibodyShop, Grusbakken, Denmark).
Induction of GFP production in LDR cells can be assayed using a laser scanning microplate cytometer in a format suitable for high-throughput screening.
In order to ensure we can control our data for any influence of vitamin D status, frozen serum will be assayed using a Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) method to obtain a 25-OH Vitamin D quantification.
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The cells were assayed using a luciferase assay kit 24 h after transfection.
24h post-transfection, the cells were assayed using a luciferase assay kit (Promega, Madison, WI, USA).
24 h post-transfection, the cells were assayed using a luciferase assay kit.
At 24 h post-transfection, the cells were assayed using a luciferase assay kit.
Peroxidase activity was assayed using a spectrophotometer according to (Shannon et al. 1996).
RNA unwinding activity of ZIKV helicase was assayed using a radiolabeled dsRNA substrate.
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