Residual DNA and enzyme impurities are critical challenges in cell and gene therapy manufacturing. High-salt lysis improves yield, but also demands more from nucleases, especially under GMP conditions with strict regulatory limits.
In this white paper, you’ll learn:
- Why DNA removal is harder in salt-rich workflows
- How Saltonase® GMP-grade performs under high salt, pH and temperature
- How the Saltonase® ELISA Kit supports accurate residual enzyme detection
Applicable for:
Viral vector manufacturing workflows, including AAV, lentivirus (LV) and virus-like particles (VLPs) in GMP settings.