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Bacteria were seeded in a mineral medium containing 0.5% carboxymethylcellulose as sole carbon source for detection of cellulose activity.
Bacteria were seeded directly onto NGM plates containing 2 mM IPTG and 25 µg/ml carbenicillin.
For plate assays, bacteria were seeded into soft LB or M9 agar (0.3% agar) with or without X-gal (40 µg/ml) as indicated in text.
The bacteria were seeded with a confluent NIH 3T3 (mouse fibroblast) cell monolayer overnight for biofilm formation.
To measure bacterial growth on solid media, bacteria were seeded, left at room temperature for 48 hours and then transferred to 25°C for a further 24 hours.
The bacteria were seeded in Petri dishes of minimized scale (35 mm in diameter, Nunc #150318) with and without overlay agar (spread culture) [ 25, 26].
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Bacteria in exponential phase were seeded in a 96-well plate at a concentration of 2 to 5×104 bacteria per well in 50 µl of a solution containing 0.5% tryptone and 0.5% sodium chloride.
For determination of the frequency of bacteria per LCV, BMDMs were seeded at 2×105 cells/well on 13-mm glass coverslips and cultivated in 24-well tissue culture dishes.
When the guts of the control mice were seeded with bacteria from the obese group they too put on weight more rapidly.
Bacteria cultured in BH medium were seeded for 24 hours in DMEM (Gibco) containing 10% fetal calf serum (FCS) and 2% inulin.
For analyzing adherence of bacteria to cells, 10'000 RAW264.7 cells were seeded in 96-well plates (µ-clear bottom, half area, Greiner Bio One onee day before infection and pre-stimulated overnight with 1 µg/ml E. coli LPS (List Biological Laboratories, California).
More suggestions(17)
strains were seeded
fungi were seeded
cells were seeded
cultures were seeded
bacteria were recalled
bacteria were affected
bacteria were found
bacteria were used
bacteria were analyzed
bacteria were absorbed
bacteria were grown
bacteria were known
bacteria were examined
bacteria were recovered
bacteria were treated
bacteria were washed
bacteria were broken
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