Difference between revisions of "Part:BBa K642007:Design"
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===Source=== | ===Source=== | ||
− | The distal region of the Adh1 promoter was PCR amplified from a plasmid source of BBa_K319005 and using overlap extension PCR was fused to the amplified proximal region of the Gal1 promoter. The | + | The distal region of the Adh1 promoter was PCR amplified from a plasmid source of BBa_K319005 and using overlap extension PCR was fused to the amplified proximal region of the Gal1 promoter. The Gal1 promoter is commonly used promoter in our lab and we amplified it from a plasmid source. yeGFP was PCR amplified from a plasmid source of BBa_K319039. |
===References=== | ===References=== |
Revision as of 21:01, 24 October 2011
Constitutive Adh1 distal-Gal1 proximal promoter tagged with yeGFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 89
Illegal BsaI.rc site found at 1379
Design Notes
The yeGFP part (BBa_K319039) from last year didn't have a stop codon. In PCR amplification of this part, we added a stop codon.
Source
The distal region of the Adh1 promoter was PCR amplified from a plasmid source of BBa_K319005 and using overlap extension PCR was fused to the amplified proximal region of the Gal1 promoter. The Gal1 promoter is commonly used promoter in our lab and we amplified it from a plasmid source. yeGFP was PCR amplified from a plasmid source of BBa_K319039.