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Activation of T cells by the various stimuli was controlled by analysis of blast formation using flow cytometry.
Analytical performance was controlled by analysis of standard reference material, internal water quality control samples, and inter-laboratory comparison (Karolinska Institutet).
Accuracy and precision of the method were controlled by analysis of a commercial reference material (Seronorm SN ok0336; SERO AS, Billingstad, Norway).
Confounding by HLA-DRB1 risk alleles was controlled by analysis of the subgroup negative for known HLA-DRB1 risk alleles and by logistic regression including all data.
The integrity of RNA samples was controlled by analysis on bioanalyzer with RNA 6000 Nano assay Labship (Agilent Technologies, Santa Clara, CA, USA) and ratio integral number (RIN) was calculated.
Quantification was performed using 1 μL of the solution in a Nanodrop (ThermoScientific), and quality (profile and RNA Integrity Number (RIN) value) controlled by analysis of 1 μL of the solution in a Bioanalyzer (Agilent).
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Basal ganglia model : selection processes between channels, dynamics controlled by contraction analysis, rate-coding model of neurons based on locally projected dynamical systems (lPDS).
Performance of methods used for molecular diagnostics must be closely controlled by regular analysis of internal quality controls.
Possible influence by different experimental batches or cohorts were controlled by statistical analysis using batch variables or normalizing data with Succinate dehydrogenase [ubiquinone] flavoprotein subunit (SDHA), one of endogenous controls.
Efficiency of siRNA-mediated knockdown of CD151 on the cell surface was controlled by FACS analysis.
Digestion by McrBC was quality controlled by qPCR analysis of the promoter of the TH2B gene, which is densely methylated in all tissues except the testes [47].
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