"
Team:Cambridge/Gibson/Protocol
From 2010.igem.org
(Difference between revisions)
(→Step 1) Design Primers) |
|||
| Line 8: | Line 8: | ||
*The standard way to do this is with PCR with specialised primers | *The standard way to do this is with PCR with specialised primers | ||
| - | *We have designed a tool to help you do this: | + | *We have designed a tool to help you do this: [http://www.gibthon.org Gibthon] |
| - | + | ||
== Master mix == | == Master mix == | ||
Revision as of 10:07, 30 September 2010
Gibson Assembly: Protocols
Step 1) Design Primers
- If you wish to ligate two pieces of DNA using Gibson they must be altered so as to have 40bp of overlap with respect to each other.
//Insert diagram of two pieces of DNA with overlap
- The standard way to do this is with PCR with specialised primers
- We have designed a tool to help you do this: [http://www.gibthon.org Gibthon]
Master mix
| Volume/µl | |
| Taq ligase (40u/µl) | 50 |
| 5x isothermal buffer | 100 |
| T5 exonuclease (1u/µl) | 2 |
| Phusion polymerase (2u/µl) | 6.25 |
| Nuclease-free water | 216.75 |
| =375 |
