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Table I shows the number of intact roots remaining after various shearing times, and IgG release normalized to grinding in liquid nitrogen.
The FMD is expressed as the maximum change in diameter after cuff release normalized to the baseline diameter (% of baseline diameter).
IgG release normalized to release by grinding appeared to lag behind the number of roots that had fragmented, suggesting that a process of leakage followed fragmentation in the ultra-scale down shearing device.
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Enzyme activity was expressed as nmoles of p-nitrophenol released, normalized to the protein content of the sample.
The relative strength of strains was determined indirectly based on the amount of product or dsDNA released normalized as a percentage of the total amount available.
However, at the end of the toe release, the normalized ΣTmax values were close to Ka.
To control for interexperimental differences in adipocyte differentiation, glycerol release was normalized to the glycerol-3-phosphate dehydrogenase activity and protein content of each sample.
LDH release was normalized with respect to maximal LDH release after total cell lysis [ 9, 10].
Values for release were normalized to the GAG content of the explants.
Glutamate release was normalized to cell number and statistically analyzed by one-way analysis of variance.
Similar trends were observed when Cr release was normalized to the surface area (File S1, Figure S2).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com