Difference between revisions of "Part:BBa K3384312:Design"
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===Design Notes===
 
===Design Notes===
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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 <em>prm1</em> gene, which is a putative <em>fus2</em> promoter.
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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 <em>fus2</em> gene, which is a putative <em>fus2</em> promoter.

Revision as of 11:55, 26 October 2020

pfus2


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE 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 gene, which is a putative fus2 promoter.