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Exact(6)
Relative luciferase activity was calculated by normalizing the firefly luminescence as to the renilla luminescence.
The transcriptional activities of each constructs were calculated by normalizing the firefly luciferase activities with corresponding Renilla luciferase activities, and were reported as folds of induction compared with the activity of empty pGL 4.15 vector.
Relative luciferase activities were obtained by normalizing the firefly luciferase activity against renilla luciferase activity.
Relative MMP-1-promoter activation was derived by normalizing the firefly luciferase activity to renilla luciferase activity.
The relative luciferase activity was calculated by normalizing the firefly luciferase activity against that of the internal control (Renilla luciferase).
In addition, the promoter activity was presented as relative luciferase activity by normalizing the firefly luciferase activity to the internal control of renila luciferase activity.
Similar(54)
Relative expression of reporter constructs was determined by normalizing the ratio of Renilla luciferase activity and firefly luciferase activity to mimic NC or inhibitor NC.
Renilla luciferase activity was used to normalize the firefly luciferase activity.
Relative luminescence was measured by normalizing firefly luciferase values to those detected from a Renilla luciferase construct used as a transfection efficiency control.
Knockdown rates were calculated by normalizing Renilla luciferase activities to firefly luciferase activities, and comparing dual-luciferase ratios between the targeting amiRNAs and the non-targeting negative control amiRNA.
Knockdown rates were calculated by normalizing Renilla luciferase activities to firefly luciferase activities, and comparing dual-luciferase ratios between targeting and non-targeting control siRNAs.
More suggestions(15)
by normalizing the stay
by normalizing the alteration
by normalizing the completion
by normalizing the column
by normalizing the slope
by normalizing the follicle
by dividing the firefly
by replacing the firefly
by cloning the firefly
by normalizing the assay
by normalizing the signal
by normalizing the light
by normalizing the fluorescence
by measuring the firefly
by employing the firefly
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