Part:BBa_K5142045:Design
Compositive construct for A27L-3Stop mutagenesis
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Illegal EcoRI site found at 1243
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Illegal PstI site found at 1504
Illegal PstI site found at 1878
Illegal PstI site found at 2421 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 1
Illegal EcoRI site found at 483
Illegal EcoRI site found at 1243
Illegal EcoRI site found at 1393
Illegal EcoRI site found at 1510
Illegal EcoRI site found at 1884
Illegal XbaI site found at 16
Illegal XbaI site found at 498
Illegal XbaI site found at 1258
Illegal XbaI site found at 1408
Illegal XbaI site found at 1525
Illegal XbaI site found at 1899
Illegal SpeI site found at 463
Illegal SpeI site found at 1223
Illegal SpeI site found at 1373
Illegal SpeI site found at 1490
Illegal SpeI site found at 1864
Illegal SpeI site found at 2407
Illegal PstI site found at 477
Illegal PstI site found at 1237
Illegal PstI site found at 1387
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Design Notes
1. To prevent potential readthrough transcription when inserted into vaccinia virus genome, the GFP was transcribed in the direction reverse to the adjacent viral genes (e.g., A26L, A27L and A28L) which was driven by poxviral H5 promoter. 2. Considering the whole A26L sequence is too long as a homologous arm, we chose 500 bp sequence adjacent to A27L only to construct the recombinant element.
Source
This part is composed of the following basic parts aligned tandemly: vaccinia virus A28L (BBa_K5142010), reverse complementary GFP cds (BBa_K5142013), reverse poxviral H5 promoter (BBa_K5142012), overlapping early/late poxviral promoter (BBa_K5142011), vaccinia virus A27L-3stop (BBa_K5142007), vaccinia virus A26L (partial) (BBa_K5142014).