Sentence examples for preparing assay from inspiring English sources

The methodology was modified to allow the analysis of amikacin in BAL over a concentration range of 2.50 to 50.00 μg/mL by simply preparing assay calibrators and quality-control samples in BAL fluid; no further modification of the assay procedure was required.

To prepare assay plates, we poured 3 ml NGM into 35 mm Petri plates one day prior to tracking worms.

The curve fit analysis was based on averaged duplicate measurements of assay calibrators provided with each assay kit and prepared in assay buffer as per manufacturer's instructions.

The isolation and characterization of CTCs is more technically challenging than preparing and assaying cfDNA.

All samples were assayed in triplicate, and two blanks were prepared per assay for the sample and reagents.

For control plates, a choline concentration curve ± HC-3 was prepared in assay buffer at 5× the final concentration to be assayed.

Moreover, moiety-heterologous haptens were designed and prepared for assay sensitivity improvement.

After aspiration, the plates were washed with 3 × 300 μL PBST buffer to prepare for assay application (Gill et al. 2006).

Serum samples were heat inactivated at 56°C for 30 min, and serial 2-fold dilutions were prepared with assay buffer.

Working dilutions were prepared in assay medium immediately before use as described below.

Standards (100 μl) and samples prepared in assay buffer were added to the wells.