吉尔森半制备/制备色谱系统

The application principle injected samples onto a separation column to cleave individual peaks and transfer these peaks onto secondary dual chiral columns for separation. Automated and complete purification of analytes with high resolution of the separated enantiomers provided speedy purification, efficient separation, and simplified collection of chiral analytes, eliminating the need for extensive sample cleanup.

DNA fragments ranging from 25 to 2000 base pairs (bp) in length were used for the development of a suitable gradient for separating DNA molecules