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. 2020 Mar 10;7:100855. doi: 10.1016/j.mex.2020.100855
Parameter Original Protocol Modified Protocol
Heat shock prior to electroporation 40 °C, 350 rpm, 30 min in microtube Eppendorf Thermomixer Same
sgRNA expression vector plasmid.
pPH331
1 µg 1 µg or 2 µg
Cas9 expression vector plasmid, pPH187 2 µg 2 µg or 4 µg
Electroporator NEPA21, Complex waveform
Fig. 1(A)
Bio-Rad Gene Pulser II, simple exponential pulsesFig. 1(B)
Post electroporation recovery 500 µL TAP+Arg
24-well plate
Wrap in aluminum
Same
Recovery temp, 1st & 2nd day 1st day 33 °C
2nd day 22 °C
1st day 30–32 °C
2nd day 21–25 °C
Recovery Plates 1.5% agar, TAP + 100 mg/L-arginine + 3 mg/mL yeast extract + 2 mg/mL tryptone + 10 mg/mL paromomycin Same. Plates without yeast extract and tryptone were also tested; three 100 mm plates per electroporation
Wait time to count colonies 7–10 days 19–25 days