Difference between revisions of "Part:BBa K208011:Design"
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<partinfo>BBa_K208011 short</partinfo> | <partinfo>BBa_K208011 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
| − | + | This is a variation of a Lac promoter with an attached ribosome binding site. The RBS was attached to the promoter and made into a BioBrick to simplify the composite part construction process as cutting and ligating a small sequence, like a ribosome binding site, can be difficult. | |
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===Source=== | ===Source=== | ||
| − | + | This part was designed by the USU iGEM 2009 team and synthesized by DNA 2.0. The part was cut and ligated into a BioBrick plasmid, pSB1AK3 and sequenced. | |
===References=== | ===References=== | ||
| + | Please consult the original pages for these parts for more details on their functionality. | ||
Latest revision as of 01:03, 23 October 2009
Lac Reg. Lambda Hybrid (BBa_R0011) and RBS (BBa_B0034)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This is a variation of a Lac promoter with an attached ribosome binding site. The RBS was attached to the promoter and made into a BioBrick to simplify the composite part construction process as cutting and ligating a small sequence, like a ribosome binding site, can be difficult.
Source
This part was designed by the USU iGEM 2009 team and synthesized by DNA 2.0. The part was cut and ligated into a BioBrick plasmid, pSB1AK3 and sequenced.
References
Please consult the original pages for these parts for more details on their functionality.