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文献和实验Transformation of E. coli by Electroporation
100% ethanol 70% ethanol 0.5X TE SOC medium transformation plates I. Preparation of E. coli cells
Maxiprep of plasmid DNA from E. coli
Grow a single colony of E. coli overnight in 50mL LB broth + selective markers at 37°C. The next morning, put 850μL of the culture in each of two Eppendorf tubes, add 150μL sterile 50% glycerol, and store at -80°C. Pour as much culture as will fit
Transformation DNA fragments (or plasmid DNA) into competent E. coli
Transformation DNA fragments (or plasmid DNA) into competent E. coli * Caution: Use aerosol protecting tips if selection of transformed cells is not based on X-gal strategy. 1.Remove competent cells (E.coli DH5aTM from GIBCO BRL) from -70 ℃
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