Difference between revisions of "Part:BBa K2916013:Design"
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===Design Notes=== | ===Design Notes=== | ||
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The sequence was extracted from the pET21a-AsnRS-His plasmid and expressed in the BL21 (DE3) E.coli strain. | The sequence was extracted from the pET21a-AsnRS-His plasmid and expressed in the BL21 (DE3) E.coli strain. | ||
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===Source=== | ===Source=== | ||
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===References=== | ===References=== | ||
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+ | Cell-free translation reconstituted with purified components. Shimizu Y, Inoue A, Tomari Y, Suzuki T, Yokogawa T, Nishikawa K, Ueda T. Nat Biotechnol. 2001 Aug;19(8):751-5. doi: 10.1038/90802. 10.1038/90802 PubMed 11479568 |
Revision as of 10:43, 24 July 2019
GlyRS protein equipped with a 6x HIS affinity tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 2989
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1737
Illegal AgeI site found at 471
Illegal AgeI site found at 2859 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 958
Design Notes
The sequence was extracted from the pET21a-AsnRS-His plasmid and expressed in the BL21 (DE3) E.coli strain.
Source
http://www.addgene.org/124106/
References
Cell-free translation reconstituted with purified components. Shimizu Y, Inoue A, Tomari Y, Suzuki T, Yokogawa T, Nishikawa K, Ueda T. Nat Biotechnol. 2001 Aug;19(8):751-5. doi: 10.1038/90802. 10.1038/90802 PubMed 11479568