Composite

Part:BBa_K1983015:Design

Designed by: Vykintas Jauniškis   Group: iGEM16_Vilnius-Lithuania   (2016-10-13)
Revision as of 10:22, 22 October 2016 by Vykintas (Talk | contribs)


PheP and tRNA-Phe under constitutive promoters


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 98
    Illegal NheI site found at 1669
    Illegal NheI site found at 1692
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This part has an XbaI site between RBS (J61132) and PheP gene (K1983013) because it was created by fusing (K1983014) with (K1983011).

Since one of the fused parts is a composite biobrick (K1983014) comprised of a promoter, RBS, coding gene and terminator, with XbaI it is more adaptable regarding the regulation of this gene. In addition, having only an XbaI site in the resulting fused part (K1983015), it can be still be combined with other biobricks when digested with SpeI and PstI.

Primers

Primers used for amplification of the fragment:
Uni-FW: GTAGAATTCGCGGCCGCTTCTAG
Uni-RV: GTAGACTGCAGCGGCCGCTACTAG

Primers used for colony PCR screening:

For pSB1C3:
VF2: tgccacctgacgtctaagaa
VR: attaccgcctttgagtgagc


Source

BBa_K1983015

References