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Pearson's correlation coefficient (R) was used to assess the reproducibility of the assay between near-serial sections of the index array.
However, more efforts are needed to harmonize the assay between veterinary diagnostic labs.
I want to study how APOBEC3-induced mutagenesis gives bladder cancer cells a survival advantage by performing a competition assay between cells expressing APOBEC3 in an inducible system and those that do not.
In a competitive binding assay between artemisinin and the four biotinylated probes, we searched for the trypanosomal target protein of artemisinin.
However, less agreement (Kappa = 0.2 0.6) between microarray results were observed when using different hybridization buffers, indicating this parameter as being highly critical when transferring a standard microarray assay between laboratories.
The result of the antagonism assay between organisms of individual combination is presented in Table 5.
BiFC plasmids pRTVnVN-SPIN6, pRTVnVC-OsRac1, and control pRTVcVC-LUC were used for the interaction assay between SPIN6 and OsRac1.
In our study, cell viability was determined by colorimetric assay between the cell supernatant and WST-8 kit.
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A reproducibility study was designed to assess within-assay, between-day, and interlaboratory variability of three real-time PCR assays targeting HPV 16, HPV 18, and the human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) pseudogenes.
Analytical precision was defined as intra-assay (within-run) and inter-assay (between-run) repeatability of results produced by Kalon, as performed by Technologist-Jr.
The intra-assay (within-plate) CV for the ELISA was 0·1 12·5 % and the inter-assay (between-plate) CV was 0·2 12·3%%.
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