The Tool allows you to search for restriction enzymes by name, recognition sequence or overhang. Enter your sequence using single letter code nomenclature, and the tool will identify the right enzyme for the job. If the enzyme has isoschizomers (enzymes with the same recognition sequence and cut site) or neoschizomers (enzymes with the same recognition sequence but a different cut site), a list of these enzymes is provided. Select any of the listed enzymes to see further details on cut site, overhang and required incubation conditions. Once you have selected an enzyme, you can select a second enzyme and retrieve information for double digests. Choose a second enzyme from the list of enzymes with the selected level of activity, the display will show the range of buffer choices for a double digest with both selected enzymes. If no suitable enzyme with the selected co-activity is found, you can adjust the co-activity level to expand the list of enzyme choices. A red background indicates that the enzyme/buffer combination exhibits star activity.
** This tool is collected to facilitate your research. Currently GenScript does not have restriction enzymes for sale and will not be responsible for any problems caused by using this tool.
You can find an enzyme by entering the name, recognition sequence or overhang sequence. Promega enzymes are indicated in orange.
Select "Name", and enter the name of your enzyme into the searchbox.
Select "Sequence", and enter the recognition sequence into the searchbox. Only exact matches will be returned when the "wildcard match" is turned OFF. The following IUPAC codes can be used when the wildcard match is turned ON:
N = A,T,C or G (any nucleotide)
Y = T or C (pyrimidine)
R = G or A (purine)
M = A or C (amino)
K = G or T (keto)
S = G or C (strong interactions: 3 H bonds)
W = A or T (weak interactions: 2 H bonds)
B = G, T or C (not A)
V = G, C or A (not T or U)
D = G, A or T (not C)
H = A, C or T (not G)
Search by specific 3' or 5' overhang, or list all blunt enzymes.
Once you have selected an enzyme, you can select a second enzyme and retrieve information on suitable buffers for double digests. Activity data in Promega buffers are not available for all enzymes.
Recognition sequence, cut site and overhang are indicated for each enzyme.
If the enzyme has isoschizomers (enzymes with the same recognition sequence and cut site) or neoschizomers (enzymes with the same recognition sequence but a different cut site), a list of these enzymes is provided. Select any of the listed enzymes to see further details on cut site, overhang and required incubation conditions.
For Promega enzymes, the incubation temperature, supplied buffer, and activity in other Promega buffers is provided.
A red background indicates that the enzyme/buffer combination exhibits star activity.
For enzymes that have been tested in Promega buffers, you can find information on suitable buffers to use for double digests. To use the double digest tool:
A red background indicates that the enzyme/buffer combination exhibits star activity.