Difference between revisions of "Part:BBa K3600009"
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===Functional Parameters=== | ===Functional Parameters=== | ||
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Latest revision as of 02:53, 28 October 2020
prGSH1-yomScarlet-I-tADH1
This cassette was assembled from 6 part plasmids via Golden Gate assembly using the BsmbBI restriction enzyme. The two connectors (pYTK002 and pYTK072), as well as the terminator (pYTK053) and the Ampicilin resistance/backbone (pYTK095) part plasmids are part of the YTK toolkit developed by Lee et al.1 and can be ordered online.
The promoter part plasmid (BBa_K3600003) and the reporter part plasmid (BBa_K3600010) were synthesized by us.
Usage and Biology
This cassette contains the GSH1 promoter upstream of a reporter gene (mScarlet-i). GSH1 is a stress response gene in s.cerevisiae that is regulated by the YAP1 master regulator2. This cassette is then assembled with a part plasmid containing Lys2 homology sequences (BBa_K36000012) in another Golden Gate BsmBI assembly, to give a final integration cassette (BBa_K3600016).
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal SpeI site found at 2811
Illegal PstI site found at 2820
Illegal NotI site found at 924
Illegal NotI site found at 2830 - 21INCOMPATIBLE WITH RFC[21]Illegal suffix found in sequence at 2413
Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal BglII site found at 2284
Illegal XhoI site found at 1531 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 936
Illegal EcoRI site found at 1666
Illegal XbaI site found at 945
Illegal XbaI site found at 1843
Illegal SpeI site found at 2811
Illegal PstI site found at 2820
Illegal NgoMIV site found at 2768 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1528