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The number of single cell WGA samples tested by each assays is given in Fig 2D.
As each assays has its specific pitfalls, we performed two assays to be sure that the ability of dynein to collapse the spindle was not due to a specific type of assay.
Similar(58)
Ms. Obardors's Carmen assays each encounter in the way Martin might.
Each assay was performed triplicate.
Fresh solutions were prepared before each assay.
Three replicates of each assay were performed.
Each assay was performed in quadruplicates.
Detection limit was determined for each assay.
Each assay format was designed as an inhibition assay.
Each assay was set up at least in duplicate.
Erythrocytes were maintained 108 cells per mL for each assay.
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