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The "MeSH Term Active" retrieves assays in which only active compounds are annotated with the query MeSH term.
Titration assays in which T. harzianum DNA from distinct strains was varied further underscored the specificity of the probes.
The adopted approach was based on activity/inhibition assays in which the reduction of enzyme activity was denoted by a decrease of fluorescence.
Methodology includes static assays in which membrane's samples were immersed in a cleaning solution for over 12 or 24h at a temperature of 25 to 40°C.
This was in marked contrast to the efficiency of 1stST observed in single-round cell infection assays, in which ssDNA and U3 U5 copy numbers were indistinguishable.
In assays in which multiple co-culture aggregates were cultured within a single hydrogel, we observed directional invasion of sprouts preferentially towards the other aggregates within the hydrogel.
Using these criteria, 544 of 570 (95%) of all assays in which the PHA control was performed were interpretable.
Therefore, we first performed affinity co-precipitation assays, in which we aimed to pull down different AChR populations.
Assays in which catalase was replaced by either superoxide dismutase or β-amilase were included as negative controls.
Our analysis is based on single-choice courtship assays, in which a sexually mature male is offered a wild-type receptive virgin female or mature male.
This was confirmed by human serum assays, in which there was no difference in the survival of isogenic strains with and without IS1301 with associated polymorphisms (Figure 3B).
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