Difference between revisions of "Part:BBa K3384312:Design"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K3384312 short</partinfo> | ||
+ | <partinfo>BBa_K3384312 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | ===Design Notes=== | ||
+ | It was obtained by PCR amplification using <em>Saccharomyces cerevisiae</em> BY4741 genome as template. The amplified product is a 331bp sequence upstream of the Fus2 coding sequence, which is a putative <em>fus2</em> promoter. |
Latest revision as of 07:42, 27 October 2020
pfus2
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
It was obtained by PCR amplification using Saccharomyces cerevisiae BY4741 genome as template. The amplified product is a 331bp sequence upstream of the Fus2 coding sequence, which is a putative fus2 promoter.