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Correlations were assessed using a scatter graph and Spearman correlation coefficient (rs).
Don't use a scatter rock when a pebble shot will do the job.
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.
Creatinine was assayed using a spectrophotometric assay.
Luciferase assays were done using a luciferase assay kit (Promega).
For the samples using the viability assay, the initial step included using a side scatter width setting to exclude obvious doublets.
The scatter sinogram was estimated from the emission data and the attenuation maps using a single scatter simulation algorithm [ 28].
Similarly, we performed size distribution analysis in various solutions such as water, DMEM media, and DMEM with 10% FBS using dynamic light scattering assay.
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