Difference between revisions of "Part:BBa K1899008"
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<partinfo>BBa_K1899008 short</partinfo>
 
<partinfo>BBa_K1899008 short</partinfo>
  
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With all the essential elements for a circuit to function, this part could be used independently in the project to estimate the promoter stength of the phlFp. Since it contains a green fluorescence protein reporter gene, GFP protein would be produced during the characterisation, thus, the intensity of the GFP could be used to estimate the strength of <i>phlFp</i> and compare it to that of the other two promoters in our project, <i>lacp</i> and <i>tetp</i>.
+
With all the essential elements for a circuit to function, this part could be used independently in the project to estimate the promoter stength of the phlFp. Since it contains a green fluorescence protein reporter gene, GFP protein would be produced during the characterization, thus, the intensity of the GFP could be used to estimate the strength of <i>phlFp</i> and compare it to that of the other two promoters in our project, <i>lacp</i> and <i>tetp</i>.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 18:18, 14 October 2016


phlFp-E0240

With all the essential elements for a circuit to function, this part could be used independently in the project to estimate the promoter stength of the phlFp. Since it contains a green fluorescence protein reporter gene, GFP protein would be produced during the characterization, thus, the intensity of the GFP could be used to estimate the strength of phlFp and compare it to that of the other two promoters in our project, lacp and tetp.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 737