Removal reagent simply and effectively removes the DNase and divalent cations in a single step, reducing sample loss due to phenol extraction, and preventing enzyme-independent strand scission
Turbo DNA-free treatment and removal reagents are designed for the removal of contaminating DNA from RNA samples using a specifically engineered DNase, Turbo DNase, and the subsequent removal of the DNase after treatment.
Turbo DNase exhibits a much greater binding efficiency than wild type DNase I.
This is important for complete removal of DNA from a sample since the concentration of the cleavable substrate is reduced as the DNase digestion progresses.
A novel DNase removal reagent simply and effectively removes the Turbo DNase and divalent cations in a single step, reducing sample loss due to phenol extraction, and preventing enzyme-independent strand scission.
