Difference between revisions of "Part:BBa K5097017"

 
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<partinfo>BBa_K5097017 short</partinfo>
 
<partinfo>BBa_K5097017 short</partinfo>
 
   
 
   
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===Usage and Biology===
 
===Usage and Biology===
  
 
The 2024 Oneonta iGEM team pHish and CHIPs used RFP as a reporter protein to test the function of pH-sensitive regulatory elements that control gene expression. As a companion to these studies, we investigated what effect pH might have on the fluorescence of RFP. To do this, we generated a constitutively expressed RFP (BBa_K5097015) that is modified on the C-terminal to remove the native stop codon, and then with the addition of an AGVG linker and 6x His tag.  A double-stop codon was added at the end.
 
The 2024 Oneonta iGEM team pHish and CHIPs used RFP as a reporter protein to test the function of pH-sensitive regulatory elements that control gene expression. As a companion to these studies, we investigated what effect pH might have on the fluorescence of RFP. To do this, we generated a constitutively expressed RFP (BBa_K5097015) that is modified on the C-terminal to remove the native stop codon, and then with the addition of an AGVG linker and 6x His tag.  A double-stop codon was added at the end.
  
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Latest revision as of 11:54, 30 September 2024


RFP with 6X His

Usage and Biology

The 2024 Oneonta iGEM team pHish and CHIPs used RFP as a reporter protein to test the function of pH-sensitive regulatory elements that control gene expression. As a companion to these studies, we investigated what effect pH might have on the fluorescence of RFP. To do this, we generated a constitutively expressed RFP (BBa_K5097015) that is modified on the C-terminal to remove the native stop codon, and then with the addition of an AGVG linker and 6x His tag. A double-stop codon was added at the end.

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 AgeI site found at 630
    Illegal AgeI site found at 742
  • 1000
    COMPATIBLE WITH RFC[1000]