DNA
Part:BBa_K2100039:Design
Designed by: Wangui Mbuguiro Group: iGEM16_MIT (2016-10-17)
pEXPR pBM3R1 - eYFP
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 242
Illegal PstI site found at 481 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 242
Illegal NheI site found at 115
Illegal PstI site found at 481
Illegal NotI site found at 4 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 242
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 242
Illegal PstI site found at 481 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 242
Illegal PstI site found at 481
Illegal AgeI site found at 264 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 108
Illegal BsaI site found at 235
Design Notes
This composite part expression vector was created by an LR reaction. It is a promoter (flanked by L4, R1 sites) and a gene (flanked by L1, L2 sites) cloned into a backbone that has a negative selection marker between R4 and R2 sites. This part adheres to RFC 65 for recombination based cloning of mammalian parts.
Source
mammalian genomic sequence.