Difference between revisions of "Part:BBa K2271066:Design"
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+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K2271066 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | ===Design Notes=== | ||
+ | The part was designed as a marker for the peroxisomal lumen. | ||
+ | |||
+ | ===Source=== | ||
+ | |||
+ | The Promoter, mRuby and Terminator were obtained from A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly from Lee <i>et al.</i> (2015). [1] | ||
+ | <br> | ||
+ | ePts1 was synthesized by IDT. | ||
+ | |||
+ | ===References=== |
Revision as of 10:25, 31 October 2017
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 860
Illegal BamHI site found at 1577
Illegal XhoI site found at 1613 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The part was designed as a marker for the peroxisomal lumen.
Source
The Promoter, mRuby and Terminator were obtained from A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly from Lee et al. (2015). [1]
ePts1 was synthesized by IDT.