Difference between revisions of "Part:BBa K2429017:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This part is human-codon optimized. We found a BsaI site in the middle of mKate Exon 2, so we use site-directed mutagenesis to change the base pair at position 1450 from a G to an A. We also mutated the HBG Intron 2 at position | + | This part is human-codon optimized. We found a BsaI site in the middle of mKate Exon 2, so we use site-directed mutagenesis to change the base pair at position 1450 from a G to an A. We also mutated the HBG Intron 2 at position 888 from a C to an A because the paper we were referencing had mutated the HBG intron in the same way. |
− | + | ||
+ | This basic part entry vector is flanked by L1 and L2 sites, which are used to denote a gene. | ||
===Source=== | ===Source=== | ||
− | The | + | The HBG intron came from HEK genome, and mKate from jellyfish. |
===References=== | ===References=== |
Latest revision as of 14:58, 26 October 2017
2 Exon mKate-HBG Reporter
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1582
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1582
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1582
Illegal BamHI site found at 1 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1582
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1582
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1487
Illegal SapI.rc site found at 55
Design Notes
This part is human-codon optimized. We found a BsaI site in the middle of mKate Exon 2, so we use site-directed mutagenesis to change the base pair at position 1450 from a G to an A. We also mutated the HBG Intron 2 at position 888 from a C to an A because the paper we were referencing had mutated the HBG intron in the same way.
This basic part entry vector is flanked by L1 and L2 sites, which are used to denote a gene.
Source
The HBG intron came from HEK genome, and mKate from jellyfish.