"
Team:Hannover/Protocols/Cloning/REases
From 2014.igem.org
(Difference between revisions)
| (6 intermediate revisions not shown) | |||
| Line 5: | Line 5: | ||
<html> | <html> | ||
<body> | <body> | ||
| - | <h1><a href="https://2014.igem.org/Team:Hannover/Protocols | + | <h1><a href="https://2014.igem.org/Team:Hannover/Protocols">Protocols</a> / Restriction Enzyme Cleavage (Digest)</h1> |
| - | + | <p class="text">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 orientated genetic recombination, two endonucleases generating different overhangs were chosen for each cloning step. The reaction mix used here is shown in the following table. </p> | |
| - | <p class="text">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 | + | <br><br> |
| - | + | <h2>Table 1: Reaction Mixes and Temperature Programs for the Digest.</h2> | |
| - | <h2>Table 1: Reaction | + | <table align="line" width="800px"><tr><td><table> |
| - | <table align="line" width=" | + | |
<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> |
<tr><td>1.00</td><td>enzyme x</td></tr> | <tr><td>1.00</td><td>enzyme x</td></tr> | ||
<tr><td>1.00</td><td>enzyme y</td></tr> | <tr><td>1.00</td><td>enzyme y</td></tr> | ||
<tr><td> -</td><td>500 ng DNA</td></tr> | <tr><td> -</td><td>500 ng DNA</td></tr> | ||
| - | <tr><td colspan="2">ad 20 µl | + | <tr><td colspan="2">ad 20 µl H<sub>2</sub>O</td></tr></table></td><td><table colspan="2" ><tr><td><b>Cycler Program</b></td></tr><tr><td>Step</td><td>Temperature [°C]</td><td>Time [min]</td><td>Cycle no.</td></tr><tr><td>1.</td><td>37</td><td>10.0</td><td>1</td></tr><tr><td>2.</td><td>80</td><td>5.0</td><td>1</td></tr></table></td></tr></table> |
<br><br> | <br><br> | ||
Latest revision as of 23:34, 17 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 orientated 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.
|
| |||||||||||||||||||||||||
