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Team:Grenoble/Biology/Protocols/BB
From 2012.igem.org
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<h2>Protocol</h2> | <h2>Protocol</h2> | ||
Following are the instructions from the | Following are the instructions from the | ||
| - | <a href="http://partsregistry.org/Help:Distribution_Kits">Part Registry</a>. | + | <a href="http://partsregistry.org/Help:Distribution_Kits" target="blank">Part Registry</a>. |
<br/> | <br/> | ||
<br/> | <br/> | ||
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We recommend that you do not remove the foil cover, as it could lead to cross contamination between the wells.</li> | We recommend that you do not remove the foil cover, as it could lead to cross contamination between the wells.</li> | ||
<br/> | <br/> | ||
| - | <li>Pipette 10µL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully resuspended. We recommend that you do not use | + | <li>Pipette 10µL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully resuspended. We recommend that you do not use TE to resuspend the dried DNA.</li> |
<br/> | <br/> | ||
<li><a href="http://partsregistry.org/Help:Transformation_Protocol">Transform</a> 1 or 2µL of the resuspended DNA into your desired competent cells, | <li><a href="http://partsregistry.org/Help:Transformation_Protocol">Transform</a> 1 or 2µL of the resuspended DNA into your desired competent cells, | ||
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<li>Use the resulting culture to <a href="http://openwetware.org/wiki/Miniprep/Kit-free_high-throughput_protocol"> miniprep</a> | <li>Use the resulting culture to <a href="http://openwetware.org/wiki/Miniprep/Kit-free_high-throughput_protocol"> miniprep</a> | ||
| - | the DNA | + | the DNA AND make your own glycerol stock (for further instruction on making a glycerol see |
| - | <a href="http://openwetware.org/wiki/Endy:Making_a_long_term_stock_of_bacteria"> this page</a>). We recommend using the miniprepped DNA to run | + | <a href="http://openwetware.org/wiki/Endy:Making_a_long_term_stock_of_bacteria"> this page</a>). We recommend using the miniprepped DNA to run QC tests, such as restriction digests and sequencing.</li> |
</ol> | </ol> | ||
Revision as of 14:55, 3 September 2012
BioBricks extraction
Goal
Recover the BioBricks from the plate sent by iGEM.Protocol
Following are the instructions from the Part Registry.To use the DNA in the Distribution Kit you may follow these instructions:
- With a pipette tip, punch a hole through the foil cover into the corresponding well of the Biobrick™-standard part that you want. Make sure you have properly oriented the plate. We recommend that you do not remove the foil cover, as it could lead to cross contamination between the wells.
- Pipette 10µL of dH2O (distilled water) into the well. Pipette up and down a few times and let sit for 5 minutes to make sure the dried DNA is fully resuspended. We recommend that you do not use TE to resuspend the dried DNA.
- Transform 1 or 2µL of the resuspended DNA into your desired competent cells, plate your transformation with the appropriate antibiotic and grow overnight.
- Pick a single colony and inoculate broth (again, with the correct antibiotic) and grow for 16 hours.
- Use the resulting culture to miniprep the DNA AND make your own glycerol stock (for further instruction on making a glycerol see this page). We recommend using the miniprepped DNA to run QC tests, such as restriction digests and sequencing.
