The phrase "assay list" is correct and usable in written English.
It can be used in contexts related to scientific or laboratory settings, where a list of assays or tests is being referenced.
Example: "Before starting the experiment, please review the assay list to ensure all necessary tests are included."
Alternatives: "test list" or "analysis list".
Expert judgment, supplemented by targeted literature searches, was used to generate the assay list.
A full assay list with raw and normalized threshold cycle (C t) values is provided in Additional file 3. To capture biological variability within cell lines, we measured up to four independent RNA samples per line.
Real-time quantitative PCR experiments of 93 commercially available Taqman Gene Expression Assays targeting NFκB-related genes were performed in a 7900HT RT-PCR system in a TLDA format (assay list in Supplementary Material, Table S1), which functions as an array of reaction vessels for the PCR step.
The interlaboratory differences observed in this study were not due to sample handling or technical skills since variation of sample handling was minimized by following a standardized operational procedure developed for each assay listed in Table 1 and since good intralaboratory and intra-assay reproducibility was achieved within each matrix type and within each assay platform.
Most of the fibrinolytic enzymes of microbial origin exhibit multispecificity towards various substrates (Yogesh and Halami 2015; Wang et al. 2006), and majority of the assays listed (Table 1) do not help in determining this.
Results from the ECD assay are at the lower end of detection for the assays listed in their publication.
The behavioral assays listed below were performed at 4, 6, 8, 10 and 12 weeks of age, unless otherwise noted.
Quantitative PCR was carried out using Taqman Gene Expression Assays (Life Technologies) using the gene expression assays listed below.
Compared to the assays listed above, only limited guidelines are available on the NRU assay (Andreoli et al., 2003; King and Jones, 2003).
Table 2 summarizes the control studies for the three viability assays, listing the absorbance or fluorescence value for each Ag-nps type that shows a significant interaction.
All donations were screened for anti-HIV, anti-HCV, and HBsAg using the assays listed in Table 2. Enzyme immunoassays were used for anti-HIV and anti-HCV.
