Primer
LE Promote

Part:BBa_K1539089:Design

Designed by: Coleen Tran   Group: iGEM14_GeorgiaTech   (2014-10-10)


LE Promoter Primer


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 11
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 24
    Illegal NheI site found at 47
    Illegal NotI site found at 2
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 11
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 11
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Primer design could not retain the EcoRI site but once the construct (promoter->RBS->gene) is reinserted into pSB1C3 backbone, EcoRI is site is reestablished.

The promoter was chosen from the Anderson Promoter Library with a relative transcription rate of 0.06 compared to the Anderson Promoter Consensus Sequence.

Source

Primer was ordered from IDT.

References