Difference between revisions of "Part:BBa K3753012:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | UAS<sub>CIT</sub>-pTEF is synthesized by fusing three UAS<sub>CIT</sub> tandem to the <em>tef2</em> promoter (BBa_K3753003). UAS<sub>CIT</sub> was obtained by PCR amplification using <em>Saccharomyces cerevisiae</em> BY4741 genome as template. The amplified product is a 275bp sequence upstream of the <em>cit2</em> promoter start codon. | + | UAS<sub>CIT</sub>-pTEF is synthesized by fusing three UAS<sub>CIT</sub> tandem to the <em>tef2</em> promoter (<partinfo>BBa_K3753003</partinfo>). UAS<sub>CIT</sub> was obtained by PCR amplification using <em>Saccharomyces cerevisiae</em> BY4741 genome as template. The amplified product is a 275bp sequence upstream of the <em>cit2</em> promoter start codon. |
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===Source=== | ===Source=== |
Revision as of 14:15, 16 October 2021
UASCIT-pTEF
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 845
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 845
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 845
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 845
Illegal NgoMIV site found at 1367 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
UASCIT-pTEF is synthesized by fusing three UASCIT tandem to the tef2 promoter (BBa_K3753003). UASCIT was obtained by PCR amplification using Saccharomyces cerevisiae BY4741 genome as template. The amplified product is a 275bp sequence upstream of the cit2 promoter start codon.
Source
Saccharomyces cerevisiae