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The construct is designed to capture excess organisational load – unnecessary organisational burdens that divert managers' resources from their organisational goal – as a symptom of deterioration at Business Unit level.
This construct is designed to bind reversibly to the F-actin cytoskeleton and can be used for PALM imaging due to its photoconversion from a green to a red fluorescent form upon illumination with 405 nm light.
This construct is designed to block PCNA sliding off the DNA in two ways.
Briefly, the TOP-FLASH construct is designed to measure transcriptional activation mediated by β-catenin and FOP-FLASH is the mutated counterpart of the TOP-FLASH plasmid.
The stem-loop construct is designed to detect the conformational changes in the ATP-induced aptamer binding by monitoring the change in the fluorescent intensity of the appended fluorescein when quenched in the vicinity of the AuNP.
The CASP-19 construct is designed to be separate from its predictors in particular from wealth, social connections and health (Blane et al., 2008; Hyde et al., 2003 Wiggins et al., 2004).
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A CRISPR/Cas9 construct was designed to create mutations in both SlTRM3/4 and/or SlTRM5.
The GFP gene construct was designed to express ubiquitously.
An RNA interference construct was designed to target the gene for Pns9 of RGDV, namely Trigger_G9.
First, the mini-rRNA gene construct was designed to have a rDNA promoter fused to adjacent 5'ETS segment, which has no known cleavage sites that could recruit processing factors at the transcript level.
An adenovirus-NDRG2 construct was designed to increase the expression levels of NDRG2.
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CEO of Professional Science Editing for Scientists @ prosciediting.com