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Several different procedures are used for the isolationof nucleic acids from agarose gels: electroelution,absorption to DEAE paper, absorption to glasspowder or resins, digestion of agarose with enzymes.For preparative electrophoresis, it is very importantto use highly purified agarose that is free frompolymerase and other enzyme inhibitors. Since theadvent of polymerase chain reaction (PCR) technology,tiny amounts of DNA fragments can easily beamplified for further experiments.
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