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The RdRp genes of this variant were analyzed, and the genotype could not be identified (Fig. 4b).
In brief, ROI in a selected plane from non-saturated GFP/FM4-64 confocal image stacks corrected for the mean background staining (see above) of each rescuing LAT-1 GFP LAT-1 GFPre analyzed using the 'Intensity correlation analysis' ImageJ plugin.
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The F1 cellulase enzyme produced from the E. coli codon optimized gene variant was analyzed for substrate specificity and degradation product formation using several polysaccharide substrates.
In such a case, each variant is analyzed independently.
Each type of variant was analyzed separately and then all three were analyzed jointly.
Control samples consist of all non-variant containing (NVC) tumour samples (relative to the variant being analyzed) and normal samples.
To explore this further, the R141E/A306F variant was analyzed, in turn, by analytical centrifugation and SEC-MALS.
When this variant was analyzed further by determination of the odds ratio, a low risk for CRC was observed for subjects displaying the AT genotype (Table 3).
Likewise, when RB5 oxidation by the MnP6 variant was analyzed at lower pH, there was an increase of the catalytic efficiency; it was 14-fold higher at pH 2.5 than at the usual pH 3.5 (Table 2, bottom).
The two-state denaturation of this variant was analyzed as described previously to determine its stability; the free energy of denaturation (Δ GD) and midpoint of denaturation (D1/2) are 3.8 ± 0.2 kcal/mol and 3.7 ± 0.4 M urea, respectively.
The rs10744676 KCNA5 biallelic variant was analyzed with TaqMan SNP genotyping assay in a 7900HT Real-Time polymerase chain reaction (PCR) system from Applied Biosystems by following the manufacturer's suggestions (Foster City, CA, USA).
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