Difference between revisions of "Part:BBa K1592007:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | In order to replace more convenient, we respectively added BamHI, SalI, NdeI between LIP2 prepro, E. coli ribosomal protein L2 (1-60), GS linker, YLcwp3. | + | In order to replace more convenient, we respectively added BamHI, SalI, NdeI between LIP2 prepro, E. coli ribosomal protein L2 (1-60), GS linker, YLcwp3.Also we added the 6Xhis-tag between LIP2 prepro and E. coli ribosomal protein L2 (1-60) to do verification of immunofluorescence. |
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===Source=== | ===Source=== |
Latest revision as of 04:43, 17 September 2015
LIP prepro + E. coli ribosomal protein L2 (1-60aa) + YLcwp3 Fusion
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 100
Illegal XhoI site found at 374 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 395
Design Notes
In order to replace more convenient, we respectively added BamHI, SalI, NdeI between LIP2 prepro, E. coli ribosomal protein L2 (1-60), GS linker, YLcwp3.Also we added the 6Xhis-tag between LIP2 prepro and E. coli ribosomal protein L2 (1-60) to do verification of immunofluorescence.
Source
E. coli ribosomal protein L2 was synthesized by IDT. LIP2 prepro and YLcwp3 were cloning from the plasmid JMP62 of our lab.