| 摘要 |
The invention relates to a method for parallel isolation of double- and single-stranded nucleic acids from samples containing said materials, without separating the double-and single-stranded nucleic acids. The samples are reacted with conventional lysis buffers (high salt concentrations, or low salt concentrations or with proteolytic enzymes). The sample containing nucleic acids before lysis thereof or after lysis or homogenisation is adjusted with an acidic binding buffer containing at least one non-ionic detergent in high concentration such that the total nucleic acids are adsorbed on a solid support. |
