Difference between revisions of "Part:BBa K2615007:Design"
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===Source=== | ===Source=== | ||
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− | + | Science Museum No.105,College of Marine Life Sciences, Ocean University of China | |
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===References=== | ===References=== | ||
+ | <p> | ||
+ | [http://science.sciencemag.org/content/329/5997/1355 Haurwitz R E, Jinek M, Wiedenheft B, et al. Sequence- and structure-specific RNA processing by a CRISPR endonuclease[J]. Science, 2010, 329(5997):1355-1358.] | ||
+ | </p> |
Latest revision as of 13:43, 11 September 2018
Csy4-H29A, the No.5 member of Csy4 family.
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 377
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 93
Design Notes
We designed this part by point mutation. We changed the CAC(encoding His ) to GCG(encoding Ara) on the 29th site based on wild type Csy4.
Source
Science Museum No.105,College of Marine Life Sciences, Ocean University of China
References
[http://science.sciencemag.org/content/329/5997/1355 Haurwitz R E, Jinek M, Wiedenheft B, et al. Sequence- and structure-specific RNA processing by a CRISPR endonuclease[J]. Science, 2010, 329(5997):1355-1358.]