Difference between revisions of "Part:BBa K3384312:Design"
 
(One intermediate revision by the same user not shown)
Line 6: Line 6:
  
 
===Design Notes===
 
===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 <em>prm1</em> gene, which is a putative <em>fus2</em> promoter.
+
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:
  • 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 coding sequence, which is a putative fus2 promoter.