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Flexible polyurethane foam means a flexible cellular polymer containing urea and carbamate linkages in the chain backbone produced by reacting a diisocyanate, polyol, and water.
Figure 4d shows the backbone produced by BDB− for the same image, without using the worm boundary information.
With 10 nM substrate, the reaction peaked at 25 nM transposase and then declined sharply, as judged by the amount of backbone produced.
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In contrast, substituted S,S-dioxide units located within the backbone produce a torsion of the conjugated chain.
Conjugation of starting and ending functionalizations with the polythiophene backbone produces dramatic changes in electronic (electrochemical and optical) properties.
Substitution by electron-accepting charge carriers on the conjugated polymer's backbone produces a remarkable influence on its electronic and optical properties.
Ultraviolet photodissocation (UVPD) uses ultraviolet laser pulses to cause proteins to shatter along their backbone, producing a ladder of fragments that vary in size by a single amino acid.
Xylanase (endo-β-1,4-d-xylanase, EC 3.2.1.8) exclusively catalyzes the hydrolysis of internal β-1,4-d-xylosidic linkages in the xylan backbone, producing xylooligosaccharides via a double displacement mechanism in which one conserved Glu operates as a general acid catalyst and the other Glu does as a nucleophile (Trevizano et al. 2012).
Polythiophene regular copolymers bearing amino or nitro moieties directly linked to the conjugated backbone are produced by anodic coupling of 3′,4′-diamino- or 3′,4′-dinitro-terthiophenes.
The hydrocarbon backbone was produced by ADMET polymerization followed by hydrogenation of a gem-dimethyl substituted α,ω-diene, and this material was then endcapped with alcohol-containing monoenes with varied numbers of methylenes between the alcohol group and olefin.
The backbone file produced by Mauve, a multiple-genome alignment tool (Darling et al., 2004), can be transformed into both dna_seg and comparison objects (Fig. 1B).
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