Difference between revisions of "Part:BBa K5097016"

 
Line 1: Line 1:
  
 
__NOTOC__
 
__NOTOC__
<partinfo>BBa_K5097016 short</partinfo>
+
<partinfo>BBa_K5097016 short</partinfo>  
 
+
The 2024 Oneonta iGEM team pHish and CHIPs used sBFP2 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 sBFP2. To do this, we generated a constitutively expressed sBFP2 (BBa_K156010) that is modified on the C-terminal to remove the native stop codon and added a AGVG linker and 6x His tag.  A double-stop codon was added at the end.
+
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===
 +
 +
The 2024 Oneonta iGEM team pHish and CHIPs used sBFP2 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 sBFP2. To do this, we generated a constitutively expressed sBFP2 (BBa_K156010) that is modified on the C-terminal to remove the native stop codon and added a AGVG linker and 6x His tag.  A double-stop codon was added at the end.
  
 
<!-- -->
 
<!-- -->

Revision as of 18:52, 28 September 2024


sBFP with 6X His

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
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 91