Product category:
Reagents and catalysts
News Release from: Ambion (Europe) | Subject: Turbo DNA-free
Edited by the Laboratorytalk Editorial
Team on 24 October 2003
Simplified removal of DNA contamination
for RT-PCR
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.
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