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Once the cluster evolution graph has been constructed, our methods EvolutionPred and EvoLabelPred use the clusters and their transitions to project each patient to a future moment, and predict their recovery label, respectively.
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It introduced requirements on the containment, handling, recovery, labeling, and reporting of hydrofluorocarbons (HFCs), perfluorocarbons, and sulfur hexafluoride and banned some of their applications.
We model the evolution of subpopulations of patients, for whom only two moments are available, whereby these two moments are not defined as timestamps.1 We use this model to compute a future/target state for each patient and also the recovery labels based on clinical recommendations.
Experimental procedure affects recovery Experimental procedure affects recovery Labelling is a multi-step procedure (e.g. clean-up steps, extraction or centrifugal filtration) entailing losses on every level of the applied strategy, which impairs the recovery.
This method of using labeled compounds allows for the recovery of label during cell-free conditions to calculate the amount that sticks to plastic ware.
Though she is expected to make a full recovery, the label said that "doctors have ordered her to rest her voice and completely recuperate before looking to schedule any work commitments".
In order to address this question we looked at later time points in our metabolic labeling experiments and quantified the recovery of labeled proteins after immunoprecipitation with antibodies directed against I-Aα (Figure 3 B D).
Table 3 Analysis of 5-fluorouracil in tablets by differential pulse voltammetry and recovery studies Labeled claim 100 Amount found (mg)a 96.72 RSD 3.7 t test of significant 0.43 F test of significant 0.96 Bias 2.3 Added (mg) 1 Found (mg)a 0.97 Recovered 97 RSD 1.6 Bias −3.0 aAverage of five determinations.
However, the antibiotic resistance profile of the strain to be labeled should be determined before transformation because an inherent resistance of the microbe may reduce the selective effect of the antibiotic and thereby not enable recovery of labeled strains, especially when there are low transformation frequencies.
Analyte concentrations were evaluated by considering the percent recovery of labeled internal standards.
Infiltration of L-[1-C]Asc also resulted in recovery of labeled Asc.
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