"
Team:Cambridge/Gibson/Mechanism
From 2010.igem.org
(Difference between revisions)
(→Gibson Assembly) |
(→Gibson Assembly) |
||
| Line 18: | Line 18: | ||
* Phusion polymerase | * Phusion polymerase | ||
* Taq ligase | * Taq ligase | ||
| + | <html><div style="text-align:center"><img src="https://static.igem.org/mediawiki/2010/b/b5/Cambridge-Gib2.png" style="border:1px solid black"></div></html> | ||
[[Image:Cambridge-Gib2.png|border]] | [[Image:Cambridge-Gib2.png|border]] | ||
[[Image:Cambridge-Gib3.png|border]] | [[Image:Cambridge-Gib3.png|border]] | ||
Revision as of 17:40, 18 September 2010
Gibson Assembly: Mechanism
Gibson Assembly is a means to join overlapping DNA sequences, technically it does not describe the way in which these sequences are created. However since this will be of importance to iGEM teams, we will briefly discuss this.
Creating overlapping DNA sequences
Overlapping DNA sequences can be created by PCR. We can add twenty base-pairs to the end of a sequence by using a primer which runs as follows from 5' to 3'.
20 bp of sequence to add -> 20 bp of template to anneal to.
By using two such primers we can add 20 bp of sequence A to sequence B and 20 bp of sequence B to sequence A. We are then ready to use Gibson Assembly.
Gibson Assembly
Gibson Assembly mix contains 3 enzymes:
- T5 exonuclease
- Phusion polymerase
- Taq ligase
