Difference between revisions of "Part:BBa K1595029:Design"
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<partinfo>BBa_K1595029 short</partinfo> | <partinfo>BBa_K1595029 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
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Use in conjunction with strain-expressing T7 polymerase. | Use in conjunction with strain-expressing T7 polymerase. | ||
Added GSG so EDA could easily be linked to it's associated peptide in future use. | Added GSG so EDA could easily be linked to it's associated peptide in future use. | ||
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===Source=== | ===Source=== | ||
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===References=== | ===References=== | ||
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| + | EDA: NCBI accession number P0A955 | ||
Revision as of 02:00, 14 September 2015
EDA and GSG linker
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 729
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 641
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Use in conjunction with strain-expressing T7 polymerase.
Added GSG so EDA could easily be linked to it's associated peptide in future use.
Source
Synthesized by DNA 2.0
References
EDA: NCBI accession number P0A955