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Following gentamycin treatment to ensure assessment of intracellular bacteria only, viable bacteria were determined 1 h after infection by colony forming unit (CFU/mL) determination.
At high doses, the weaponized bacteria were determined to have an incubation period of just a few hours.
To investigate a possible relationship between endophytic colonization by S. enterica and natural endophytic microbial communities, the diversity index, Shannon index (H) (Shannon and Weaver, 1963) and the species richness of natural endophytic bacteria were determined for different lettuce cultivars.
The diversity and abundance of anammox bacteria were determined by the 16S rRNA gene analysis, fluorescence in situ hybridization with specific probes and real-time quantitative PCR (qPCR).
Relative abundances of 6 well-studied bacterial taxa, total anaerobic fungi, ciliate protozoa, methanogenic Archaea and bacteria were determined using validated primer sets by real-time quantitative PCR.
Total bacterial count, and counts of Streptococcus/Enterococcus spp., Staphylococcus spp., Bacillus cereus, thermophilic, thermoduric and psychrotrophic bacteria were determined in used bedding and milk.
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The number of viable bacteria was determined by serial tenfold dilutions in BHI and plating on BHI- agar plates.
And that person's bacteria are determined in part by his diet.
The antimicrobial susceptibility of isolated bacteria was determined by using the Etest.
Antimicrobial potential of S. nemorea extracts against food spoiling yeasts and bacteria was determined in vitro by microdilution method.
Their antibacterial activity against human pathogenic Gram negative and Gram-positive bacteria was determined by agar well diffusion method.
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