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The transformants were spread on SPASC medium for selection, and several transformants were selected, based on colony size.
After transfection according to the methods mentioned above, 20 µg/ml puromycin was added into medium for selection.
For stable selection of iASPP-depleted cells, 0.5 μg/ml puromycin was added to the medium for selection.
For marker-assisted transformation, 100 mg/ml Kanamycin was added to ZCVK medium and CK medium for selection of transgenic shoots.
Forty-eight hours after the second infection, 350 μg ml−1 of hygromycin was added to the culture medium for selection of infected cells.
After 5 days, the cells were split 1 : 3, and 1 mg/mL G418 was added to the medium for selection for 10 days; the medium was replaced with fresh medium every 2 to 3 days.
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The kanamycin-resistant calluses were then cultured on the fresh selection medium for further selection and multiplication.
Six non-randomised controlled cohort studies (16 018 women) were included in the review (table 1[t1] and fig 1). 1 3 8 10 11 12 When methodological quality was assessed on the Newcastle-Ottawa scale, most studies had a medium risk for selection bias and medium to high risk for comparability and outcome assessment (table 2[t2]).
Following transfection, HK293 cells were grown in 5% CO2 to 80% confluence in DMEM supplemented with 4.5 mM glucose, 10 mM HEPES, 10% fetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin and geneticin (700 μg/ml medium) for the selection of geneticin-resistant clones, with selection medium changed every 3 4 days.
Every 3-4 weeks, transformants were selected and transferred onto fresh medium for continued selection.
The transformants were plated onto SD/-Trp medium for positive selection.
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