Difference between revisions of "Part:BBa K149001:Design"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K149001 short</partinfo> | <partinfo>BBa_K149001 short</partinfo> | ||
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− | === | + | ===Characterization=== |
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===Source=== | ===Source=== | ||
− | + | The PRP22 promoter sequence was originally extracted from S. Cervisiae, using the 2 following primers: | |
− | + | TAGTAGGATCCATTATTCTGGGCATCCGT;ATACTGAATTCCTCTAATATCTTTGTGTTACCTATGT. A BAMHI restriction site was included within the forward primer, while an EcoRV site was included within the reverse primer. This work was completed by our laboratory technician Simon St-Pierre. | |
===References=== | ===References=== |
Revision as of 20:26, 24 October 2008
Prp22 promoter
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]
Characterization
Source
The PRP22 promoter sequence was originally extracted from S. Cervisiae, using the 2 following primers: TAGTAGGATCCATTATTCTGGGCATCCGT;ATACTGAATTCCTCTAATATCTTTGTGTTACCTATGT. A BAMHI restriction site was included within the forward primer, while an EcoRV site was included within the reverse primer. This work was completed by our laboratory technician Simon St-Pierre.