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The contaminants are washed with a wash buffer (containing ethanol) and the purified DNA fragments are eluted with a low salt elution buffer or pure water. Salts, enzymes, or unincorporated nucleotides can be effectively removed from the reaction mixture without phenol extraction or alcohol precipitation. Typically, recoveries are 90 - 95% for PCR clean-up. The entire procedure can be completed in 20 minutes, and the eluted DNA is ready for use in restriction digestion, ligation, PCR, fluorescent or radioactive sequencing, and DNA labeling.
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