Difference between revisions of "Part:BBa K2996502"
 
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<center><img style="max-width: 80%" src="https://2019.igem.org/wiki/images/0/02/T--sjtu-biox-shanghai--jsf-clucfull.png" alt="" /></center>
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<center><b>Figure 1.</b> <i>PCR product of C-luciferase with J23119 promoter upstream(542bp). The ladder represents the size of DNA in bp.</i> </center>
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<center><b>Figure 1.</b> <i>Fig.1 PCR product of C-luciferase with J23119 upstream.(Lane1:product of Cluc;Lane 2:2000bp ladder)</i> </center>

Latest revision as of 23:45, 21 October 2019


C-luciferase is put downstream J23119

We used the C-terminal part of firefly luciferase in order that we could fuse it with part BBa_K2996500.The fused protein could bind specific DNA sequence to bring the C-luciferase near the other part of N-terminal part of firefly luciferase.This was aimed to signal on/off target of dCas9.In order to make the trascription of this part steady,we chose J23119 as the promoter.

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
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 302
    Illegal AgeI site found at 441
  • 1000
    COMPATIBLE WITH RFC[1000]


Figure 1. Fig.1 PCR product of C-luciferase with J23119 upstream.(Lane1:product of Cluc;Lane 2:2000bp ladder)