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Found 1 matching solution for this experiment
pONE-25A
László Beinrohr, Institute of Enzymology, Research Centre for
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Cells were plated on Minimal Dextrose (MD) plates (for vectors with HIS4 metabolic marker) and incubated for 3 days at 30°C. Freshly grown colonies from the plates were picked and grown in 20 mL or 3×100 mL YPD medium at 30°C overnight at 280 rpm. The pre-inoculum was used to inoculate 200 mL or 3×1 L Buffered Media with Glycerol (BMGY) medium and were grown for 8 hours at 30°C at 280 rpm in Erlenmeyer flasks. The flasks were not filled with more media than 25% of nominal volume. |
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Protocol tips |
Cells were plated on Minimal Dextrose (MD) plates (for vectors with HIS4 metabolic marker) and incubated for 3 days at 30°C. Freshly grown colonies from the plates were picked and grown in 20 mL or 3×100 mL YPD medium at 30°C overnight at 280 rpm. The pre-inoculum was used to inoculate 200 mL or 3×1 L Buffered Media with Glycerol (BMGY) medium and were grown for 8 hours at 30°C at 280 rpm in Erlenmeyer flasks. The flasks were not filled with more media than 25% of nominal volume. |
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