DNA

Part:BBa_K2100041:Design

Designed by: Wangui Mbuguiro   Group: iGEM16_MIT   (2016-10-17)


pEXPR pTALER21 - eYFP


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 6
    Illegal EcoRI site found at 182
    Illegal XbaI site found at 157
    Illegal PstI site found at 582
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 6
    Illegal EcoRI site found at 182
    Illegal PstI site found at 582
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 6
    Illegal EcoRI site found at 182
    Illegal BamHI site found at 311
    Illegal XhoI site found at 248
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 6
    Illegal EcoRI site found at 182
    Illegal XbaI site found at 157
    Illegal PstI site found at 582
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 6
    Illegal EcoRI site found at 182
    Illegal XbaI site found at 157
    Illegal PstI site found at 582
    Illegal AgeI site found at 365
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 326


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.

References