External link: https://www.neb.com/protocols/2014/05/07/double-digest-protocol-with-standard-restriction-enzymes
Protocol Citation: Larissa de Clauser 2022. Sequential Double Digest. protocols.io https://dx.doi.org/10.17504/protocols.io.6qpvr6m72vmk/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it’s working
Created: May 04, 2022
Last Modified: May 12, 2022
Protocol Integer ID: 61958
Keywords: restriction enzyme
Abstract
This is the Sequential Double Digest Protocol with Standard Restriction Enzymes. If there is no buffer in which the two enzymes exhibit > 50% activity, this sequential digest can be performed.
Guidelines
Digesting a DNA substrate with two restriction enzymes simultaneously (double digestion) is a common timesaving procedure. Over 200 restriction enzymes are 100% active in CutSmart™ Buffer, making double digestion simple. If you are using an enzyme that is not supplied with CutSmart Buffer, the Performance Chart for Restriction Enzymes rates the percentage activity of each restriction endonuclease in the four standard NEBuffers.
NEB's online tools, Double Digest Finder and NEBcloner will help guide your reaction buffer selection when setting up double digests.
Setting up a Double Digestion
Double digests with NEB's restriction enzymes can be set up in CutSmart Buffer. Otherwise, choose an NEBuffer that results in the most activity for both enzymes. If star activity is a concern, consider using one of our High Fidelity (HF™) enzymes.
Set up reaction according to recommended protocol. Enzyme volume should not exceed 10% of the total reaction volume to prevent star activity due to excess glycerol. For example, in a 50 µl reaction, the total amount of enzyme added should not exceed 5 µl.
If two different incubation temperatures are necessary, choose the optimal reaction buffer and set up reaction accordingly. Add the first enzyme and incubate at the desired temperature. Then, heat inactivate the first enzyme, add the second enzyme and incubate at the recommended temperature.
Depending on an enzyme's activity rating in a non-optimal NEBuffer, the number of units or incubation time may be adjusted to compensate for the slower rate of cleavage.
Setting up a Double Digestion with a Unique Buffer (designated “U”)
Setting up a Sequential Digestion
If there is no buffer in which the two enzymes exhibit > 50% activity, a sequential digest can be performed. Set up a reaction using the restriction endonuclease that has the lowest salt concentration in its recommended buffer and incubate to completion. (For reference, 1 X CutSmart and NEBuffer 1.1 do not contain any salt. 1X NEBuffer 2.1 contains 50 mM NaCl and 1X NEBuffer 3.1 contains 100 mM NaCl.)
Adjust the salt concentration of the reaction (using a small volume of a concentrated salt solution) to approximate the reaction conditions of the second restriction endonuclease.
Add the second enzyme and incubate to complete the second reaction.
Alternatively, a spin column can be used to isolate the DNA prior to the second reaction.
Before start
NEB's online tools, Double Digest Finder and NEBcloner will help guide your reaction buffer selection when setting up double digests.
Set up the following reaction using the restriction endonuclease that has the lowest salt concentration in its recommended buffer (total reaction volume 50 µl).
Note
A 50 µl reaction volume is recommended for digestion of 1 µg of substrate.
Note
The enzyme should be the last component added to reaction
Mix components by pipetting the reaction mixture up and down, or by "flicking" the reaction tube.
Quick ("touch") spin-down in a microcentrifuge. Do not vortex the reaction.
Incubate for 1 hour at the enzyme-specific appropriate temperature.
Adjust the salt concentration of the reaction (using a small volume of a concentrated salt solution) to approximate the reaction conditions of the second restriction endonuclease.
Note
Alternatively, a spin column can be used to isolate the DNA prior to the second reaction.
Add the second enzyme.
Mix components by pipetting the reaction mixture up and down, or by "flicking" the reaction tube.
Quick ("touch") spin-down in a microcentrifuge. Do not vortex the reaction.
Incubate for 1 hour at the enzyme-specific appropriate temperature.