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This assay is based on tetrazolium salt-based detection of O2− generated by xanthine oxidase and hypoxanthine.
This assay is based on the use of 2 allele-specific and one locus-specific oligonucleotide per SNP locus.
This assay is based on the Brucella spp. specific multiple IS 711 insertion sequence and therefore shows great sensitivity [ 46].
This assay is based on the cleavage activity of the light chain.
This assay is based on the TdT-mediated dUTP nick end labeling method (TUNEL method).
This assay is based on the ability of the antioxidant to scavenge the radical cation DPPH.
This assay is based on the differential ability of two nucleic acid dyes to penetrate the cell.
This assay is based on the capacity of stable free radicals of DPPH to react with hydrogen donors.
This assay is based on the cleavage of stable tetrazolium salt WST-1 by metabolically active cells to an orange formazan dye.
This assay is based on the reaction of singlet oxygen (1O2) (produced in the photodynamic reaction) with I− in the presence of ammonium molybdate as a catalyst.
This assay is based on intravenous injection of tumor cells into immunodeficient mice; 24 48 h later, the organs are extracted to detect the presence of human cells.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com