Team:Cambridge/Gibson/Introduction

From 2010.igem.org

(Difference between revisions)
(Advantages)
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* No scar created - useful for '''fusion proteins''' and '''adding an RBS''', where scars can be problematic.
* No scar created - useful for '''fusion proteins''' and '''adding an RBS''', where scars can be problematic.
* Can re-ligate linear DNA into a circle - useful for '''site-directed mutagenesis'''
* Can re-ligate linear DNA into a circle - useful for '''site-directed mutagenesis'''
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* Faster than Biobrick assembly, and works with less original.
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* Although it is roughly the same speed as [http://partsregistry.org/Help:BioBrick_Assembly standard BioBrick assembly] for ligating two fragments, Gibson is perfect for doing multi part systems, since it takes the same amount of time to ligate n pieces of DNA together as it does for 2 pieces.
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{|class="wikitable"
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|-
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|[http:partsregistry.org/Assembly:Standard_assembly Standard Assembly
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|O(n)
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|-
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|[http://partsregistry.org/Assembly:Rolling_assembly Parallel Assembly
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|0(log(n))
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|-
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|Gibson Assembly
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|O(1)
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|}
== Disadvantages ==
== Disadvantages ==

Revision as of 12:58, 30 September 2010