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Team:Hannover/Protocols/Cloning/REases
From 2014.igem.org
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<h2>Table 1: Reaction mixes and temperature programs for the digest.</h2> | <h2>Table 1: Reaction mixes and temperature programs for the digest.</h2> | ||
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<tr><td><b>Volume [μl]</b></td><td><b>Compounds of the digest</b></td></tr> | <tr><td><b>Volume [μl]</b></td><td><b>Compounds of the digest</b></td></tr> | ||
<tr><td>2.00</td><td>10 x Fast Digest Green buffer </td></tr> | <tr><td>2.00</td><td>10 x Fast Digest Green buffer </td></tr> | ||
Revision as of 11:12, 14 October 2014
Protocols / Restriction Enzyme Cleavage (Digest)
Transfer of nucleic acids was enabled by cutting sequences with restriction endonucleases. The enzymes used here identify their recognition site, cut within it, and leave behind single-stranded overhangs (sticky ends). In case no recognition site is present, attachment can be achieved by adding them to the 5´ end of PCR´s oligonucleotides. To have oriented genetic recombination, two endonucleases generating different overhangs were chosen for each cloning step. The reaction mix used here is shown in the following table.
Table 1: Reaction mixes and temperature programs for the digest.
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