This kit provides a simple and efficient method for a small amount of endotoxin-free plasmid DNA preparation. DNA is selectively adsorbed by silica gel-based column and other impurities such as proteins, salts and nucleotides do not bind. Plasmid DNA can be eluted in a small volume of Tris buffer. When using the standard protocol, the entire process takes 15-20 minutes, without phenol / chloroform extraction or ethanol precipitation. Purified DNA can be used in any downstream applications such as sequencing, transformation, restriction enzyme digestion, and ligation.

Store at Room Temperature.

*RNase A: Store at -20℃ before added to Solution I
*Solution I: After addition of RNase A, Solution I should be stored at 4℃ for frequent    use, or stored at -20℃ if not used for a long period.