Difference between revisions of "Part:BBa K3505032"

 
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<partinfo>BBa_K3505032 short</partinfo>
 
<partinfo>BBa_K3505032 short</partinfo>
  
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long
 
  
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eCFP <bbpart>BBa_K3505020</bbpart>uder control of a constitutive promoter andersonJ23115 having downstream a lac operator <bbpart>BBa_K2924013</bbpart>.
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[[File:T--Thessaly--lacoecfpmap.png|600px|thumb|none|<i><b>Fig.1:</b>pFliC-LacI-Terminator</i>]]
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===Usage and Biology===
 
===Usage and Biology===
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This Trancriscription Unit (TU) is continuesly activated exressing the eCFP protein as a reporter. The Lac operator that is downsteam the anderson exists for the lac regulated inhibition.
  
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<span class='h3bb'>Sequence and Features</span>
 
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<partinfo>BBa_K3505032 SequenceAndFeatures</partinfo>
 
  
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===Design Notes===
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The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in both a1R <bbpart>BBa_K3505008</bbpart>and a2 <bbpart>BBa_K3505009</bbpart> and has overhangs compatible for Golden Braid cloning.
  
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===Verification of cloning===
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===Functional Parameters===
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[[File:T--Thessaly--lacoecfp.png|600px|thumb|none|<i><b>Fig.2:</b>(U=Uncut C=Cut) Restriction Enzyme with HindIII. Expected bands  in bp 2847 + 804 + 146</i>]]
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<partinfo>BBa_K3505032 parameters</partinfo>
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===Experimental Use and Experinece===
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This part is used in <bbpart>BBa_K3505036</bbpart>
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===Extra Engineering Use===
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===Sequence and Features===
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<partinfo>BBa_K3505032 SequenceAndFeatures</partinfo>

Revision as of 10:27, 25 October 2020


pAndersonJ23115:lacO:RBS-eCFP -terminator


eCFP BBa_K3505020uder control of a constitutive promoter andersonJ23115 having downstream a lac operator BBa_K2924013.

File:T--Thessaly--lacoecfpmap.png
Fig.1:pFliC-LacI-Terminator

Usage and Biology

This Trancriscription Unit (TU) is continuesly activated exressing the eCFP protein as a reporter. The Lac operator that is downsteam the anderson exists for the lac regulated inhibition.


Design Notes

The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is cloned in both a1R BBa_K3505008and a2 BBa_K3505009 and has overhangs compatible for Golden Braid cloning.

Verification of cloning

Fig.2:(U=Uncut C=Cut) Restriction Enzyme with HindIII. Expected bands in bp 2847 + 804 + 146

Experimental Use and Experinece

This part is used in BBa_K3505036


Extra Engineering Use

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 11
    Illegal NheI site found at 34
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]