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According to the WHO guideline, the stability results are failing if the significant change is a 5%% or more in the assay from its initial content of API.
The obtained results show that there is no significant change on appearance and physical attributes, also the assay and impurity results show the maximum 3.4 % decrease in the assay from initial potency.
Among nulliparas, the combination of the hCG assay and a subsequent Doppler increased the positive predictive value (PPV) of the assay from 19 to 75%, without reducing its negative predictive value (NPV) for gestational vascular disorders.
Single devices to do the assay from beginning to end are now available.
This effect was not due to changing the number of females in the assay from one to four: we assayed these genotypes with four flies in the bottle assay, and found no significant differences compared to the single-female data (permutation p>0.05 for all genotypes).
Since soil microbes grow at varying rates and produce secondary metabolites at varying times, and because their isolation media is often different from our E. coli competition media, we decoupled the isolate growth and compound production phase of the assay from the resistant-sensitive competition phase.
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We found that those AFIs had less indicative value to reveal the number of Ag-specific T cells for the assays from different chamber.
Both parameters were measured on the LIA-mat using the assays from Byk-Sangtec and Brahms.
We selected plasma samples for the assays from the archived plasma pools we used in our laboratory.
The modified FLC ratio range increased the specificity of the assays (from 93% to 99%), with no loss of sensitivity.
One can calculate the calibration plot of the binding assay from the isotherm and vice versa.
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