Team:British Columbia/Protocols/GibsonAssembly

From 2012.igem.org

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This protocol closely follows the suggested protocol in the NEB Gibson Assembly guidebook.
This protocol closely follows the suggested protocol in the NEB Gibson Assembly guidebook.
   
   
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1. Using purified DNA, add 50-100ng plasmid and 2-3X molar concentration of the inserts, or 5X if using inserts of 200 bp or less. Add dH2O up to 10 uL. Set up a positive control using 10uL Gibson Assembly Positive Control.
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1. Using purified DNA, add 50-100ng plasmid and 2-3X molar concentration of the inserts, or 5X molar concentration if using inserts of 200 bp or less. Add dH2O up to 10 uL. Set up a positive control using 10uL Gibson Assembly Positive Control.

Revision as of 06:56, 2 October 2012

British Columbia - 2012.igem.org
UBC iGEM 2012 protocols

This protocol closely follows the suggested protocol in the NEB Gibson Assembly guidebook.

1. Using purified DNA, add 50-100ng plasmid and 2-3X molar concentration of the inserts, or 5X molar concentration if using inserts of 200 bp or less. Add dH2O up to 10 uL. Set up a positive control using 10uL Gibson Assembly Positive Control.


2. Add 10 uL Gibson Assembly Master Mix to each product.


3. Incubate at 50°C for 1 hour.


4. Using 2uL product, transform into competent cells. Since the Gibson Assembly Master Mix contains PEG, avoid using PEG sensitive competent cells. The provided positive control results in an amp-resistant plasmid.