Difference between revisions of "Part:BBa K3440008"

(Characterization)
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===Characterization===
 
===Characterization===
 
Due to the pandemics, we haven’t been able to use biobricks to create the iGEM Stockholm 2020 parts. Those parts were ordered as gene blocks from Integrated DNA Technologies Inc.. As a result, the sequences of the biobricks used are the same, but the scars between biobricks might differ, as well as the final size of the part.
 
Due to the pandemics, we haven’t been able to use biobricks to create the iGEM Stockholm 2020 parts. Those parts were ordered as gene blocks from Integrated DNA Technologies Inc.. As a result, the sequences of the biobricks used are the same, but the scars between biobricks might differ, as well as the final size of the part.
[[File:plateJ.png|thumb|center|500px|Transformation plate for J]]
+
[[File:T--Stockholm--platej.jpg|thumb|center|500px|Transformation plate for J]]
 
[[File:gelGJ.png|thumb|center|500px|Colony PCR gel for BBa_K3440007(G) and BBa_K3440008(J)]]
 
[[File:gelGJ.png|thumb|center|500px|Colony PCR gel for BBa_K3440007(G) and BBa_K3440008(J)]]
 
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Revision as of 00:26, 25 October 2020


RhlR with myc tag under constitutive promoter


Pconst(BBa_J23100)-RBS(BBa_B0034)-RhlR(BBa_C0071)-Myc(BBa_K823036)-DT(BBa_B0015)


Usage and Biology

Produces RhlR-Myc under constitutive promoter.

Characterization

Due to the pandemics, we haven’t been able to use biobricks to create the iGEM Stockholm 2020 parts. Those parts were ordered as gene blocks from Integrated DNA Technologies Inc.. As a result, the sequences of the biobricks used are the same, but the scars between biobricks might differ, as well as the final size of the part.

Transformation plate for J
Colony PCR gel for BBa_K3440007(G) and BBa_K3440008(J)

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 880
    Illegal BamHI site found at 301
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 776