AFTSpin EndoFree Plasmid Maxi Kit (RK30103)

This kit is capable of lysing cells using a modified SDS-alkaline lysis method. The crude extract is selectively bound with a unique endotoxin scavenger and centrifuged to remove the endotoxin. The silica-based membrane in the centrifugal adsorption column can bind the plasmid DNA in the solution selectively under the condition of high salt and low pH value, and then impurities and other bacterial components can be removed by the deproteinizing solution PR and washing solution WB. Finally the low-salt, high-pH eluent EB elutes pure plasmid DNA from the silica-based membrane.

AFTSpin EndoFree Plasmid Midi Kit (RK30105)

This kit uses a modified SDS-alkaline lysis method to lyse cells. The special Buffer P4 and the Filtration Columns 1 can effectively remove impurities such as endotoxin, protein and other impurities.The kit is suitable for extracting plasmid DNA from 5-15 mL bacterial cultures, and the whole experimental procedure of plasmid DNA extraction could be finished within 1 h. Plasmid DNA prepared is suitable for a variety of downstream applications including restriction enzyme digestion, PCR, sequencing, ligation, transformation and cell transfection.

AFTSpin EndoFree Plasmid Mini Kit (RK30102)

This kit uses a modified SDS-alkaline lysis method to lyse cells. Crude extract is selectively bound to the spin column by a unique endotoxin scavenger and centrifuged to remove endotoxin. The silicone matrix membrane in the spin column selectively binds plasmid DNA at high salt and low pH conditions, allowing for impurities and other bacterial components to be removed by Buffer PR and Buffer WB. The purified plasmid DNA is eluted from the silicone matrix membrane using low-salt and high-pH Buffer EB.

AFTSpin Plasmid Mini Kit (RK30101)

The kit is capable of lysing cells using a modified SDS-alkaline lysis method. The optimized lysate allows the silica-based membrane in the centrifugal adsorption column to selectively bind the plasmid DNA in the solution under the condition of high salt and low pH value and then removes impurities and other bacterial components by deproteinizing solution PR and washing solution WB. Finally the low-salt, high-pH eluent EB elutes the pure plasmid DNA from the silica-based membrane.
In general, a high-copy plasmid is inoculated from a single colony in 1.5-4.5 mL of LB medium supplemented with appropriate antibiotics. After overnight culture for 12-16 hours, up to 20 µg of pure plasmid can be extracted.