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Restriction Digest with NEB Enzymes

Objective

Author(s): Ada Jiang

Cut DNA fragments at specific restriction sites in preparation for analysis or downstream cloning. This protocol is based off of the NEB Restriction Digest Protocol.

Materials

Procedure

  1. Find your protocol by inputting the desired enzymes into NEBcloner 1.16.3 Restriction Enzyme Single/Double Digestion calculator. This will generate a custom protocol for a 50 µL reaction. All components can be reduced for a 25 µL reaction. Generally, digests require the following components:

    Component50 uL ReactionFinal Conc/Amount
    DNA200-1 ugn/a
    10x rCutSmart Buffer5 µL1X
    Enzyme 11 µL20 units
    Enzyme 21 µL20 units
    Nuclease-free Waterto 50 µln/a

    Table 1. General double digest protocol from NEB *5 - 10 units of enzyme per 1000ng of DNA is recommended (most enzymes are 20 units per 1 uL)

  2. Preheat thermocycler to 37°C.

  3. Set up the reaction (keeping everything on ice).

  4. Mix components by pipetting the reaction mixture up and down, or by “flicking” the reaction tube.

  5. Quick (“touch”) spin-down in a microcentrifuge. Do not vortex the reaction.

  6. Incubate at 37°C in the thermocycler for at least 15 minutes (for time-saver enzymes), up to 1 hr if needed.

  7. If appropriate for your enzyme, deactivate the reaction by incubating at 60°C or 80°C for 20 minutes.

  8. Transfer the tubes to ice. Store at -20°C if agarose gel/downstream analysis will be run in a separate lab session.