• Easy and rapid methodology to isolate high-quality DNA from very little amount of biological specimens
• Using Fresh and frozen human whole blood treated with EDTA and citrate from common blood collection system
• Employing silica-based technology using spin column and optimized buffer concentration
• Isolation of high purity genomic DNA (40-60 ng/µl) with an A260 / A280 ratio between 1.7–1.9 within a short time (less than 30 minutes)
• Reduced hands-on time and cross-contamination as well as safe control of potentially infectious specimens
• Applicable in molecular research and genetic laboratories
• Isolation of high-quality genomic DNA to be used in downstream reactions such as PCR, southern blotting, etc.
