The high quality of purified DNA samples is critical to successful genotyping studies. DNA samples with a high level of quality control and low cleavage rates are particularly essential in studies involving many genetic markers. QuickGene-610L yields DNA samples under gentle extraction conditions, without using conventional centrifugal processes. This results in higher yields of DNA with higher molecular weight, fewer cleavages and high purity. QuickGene-610L is able to extract genomic DNA from a 2ml whole blood sample, and able to process 6 samples within 12 minutes.(*) * Over 2ml of whole blood sample is adapted to pellet cells (buffy coat sample). Only three steps are required after preparing lysate samples: apply sample to cartridge, set carriage and press START. QuickGene-610L’s isolation procedure is intelligently and efficiently programmed to avoid the risk of contamination. Flat-paneled design and detachable stands allow easier maintenance and cleaning. While running QuickGene-610L, another 6 samples can be applied to another Carriage set. Continuous running of QuickGene-610L by simply switching Carriage set. QuickGene-610L can perform 60 sample extractions per hour. It really is a high throughput machine! FUJIFILM’s thin membrane effectively absorbs nucleic acids in hydrophobic solvents, separating proteins and lipids. This results in high purity and a greatly reduced processing time compared to manual methods. DNA samples isolated by QuickGene­610L require no further purification process. Extracted DNA can be directly applied to genetic analyses studies, including PCR and SNP validation. It simplifies the routine analytical workflow, and results in high throughput processes. The extracted DNA contains many proteins and chaotropic salts, and can be directly submitted for various types of analyses such as PCR, etc. About 50µ g of genome DNA can be extracted from 2ml of whole blood. DNA extracted by QuickGene has remarkable lengths of 97kbp through its gentle separation process under low-pressure conditions. Traditional spin-column extraction methods with a centrifuge often yield shorter DNA fragments than QuickGene due to the frequent cleavage of DNA molecules. The extracted DNA can be applied directly to PCR analysis. It is possible to perform PCR amplification with only a small volume of DNA. BACK