HomeFAQsWhat is the best way to generate partials using T7 Exonuclease?
FAQ: What is the best way to generate partials using T7 Exonuclease?
The enzyme should be titered to the substrate. Serial dilution of the DNA incubated for a specific time is suggested. Start with a 30 minute incubation. Incubating at room temperature can be used to slow the reaction. If the DNA is limiting the enzyme can be diluted in reaction buffer for immediate use.
You have been idle for more than 20 minutes, for your security you have been logged out. Please sign back in to continue your session.
Sign in to your NEB account
Any items placed in your cart as a guest will be lost upon sign in or leaving the site.