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Inclusion bodies from the bacterial cells were isolated and purified to homogeneity.
The Bacterial cells were isolated from culture flask and centrifuged at 7000 rpm for 10 min at 4 °C to pellet down the cells.
Bacterial cells were isolated by centrifugation at similar growth phases (24 h for control and 28 h for Al-stressed) and then re-suspended in a cell storage buffer (CSB) consisting of 50 mM Tris-HCl, 5 mM MgCl2, 1 mM PMSF (pH 7.3).
The bacterial cells were isolated by centrifugation at 6500 g for 15 min at 4 °C.
The bacterial cells were isolated by gradient centrifugation and then disrupted by ultrasonication (300 W, 15 min).
After incubation, the bacterial cells were isolated by centrifugation at 7000 × g for 10 min at 4°C.
Similar(50)
Total RNA from the bacterial cells was isolated by using the TRI reagent method (Sigma, MO) and treated with Turbo DNA-free DNase kits (Ambion, TX) as described [31].
Epitope-presenting cells were isolated by immunofluorescence staining of the bacterial cell population with monoclonal anti-Erns antibodies followed by fluorescence-activated cell sorting (FACS).
Thousands of individual cells were isolated from a mutagenized E. coli culture, and each cell was separately incubated to spawn a culture containing a billion bacterial cells that was then analyzed for DNA polymerase content.
One million viable cells were isolated.
Endothelial cells were isolated from mouse aorta.
More suggestions(17)
bacterial cells were lyzed
bacterial cells were broken
bacterial agents were isolated
bacterial cells were fixed
bacterial cells were disrupted
bacterial cells were distributed
bacterial cells were collected
bacterial samples were isolated
bacterial cells were found
bacterial cells were incubated
bacterial specimens were isolated
bacterial clones were isolated
bacterial cells were harvested
bacterial cells were gram
bacterial microflora were isolated
bacterial cells were cultured
bacterial cells were loaded
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