Difference between revisions of "Part:BBa K3505018"

(→‎Design Notes)
(→‎Design Notes)
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===Design Notes===
 
===Design Notes===
 
<p>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 pUPD2 <bbpart>BBa_K3505007<bbpart> and has overhangs compatible for Golden Braid cloning.  
 
<p>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 pUPD2 <bbpart>BBa_K3505007<bbpart> and has overhangs compatible for Golden Braid cloning.  
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The CDS has position B3-B5.
+
The CDS has position B3-B5. </p>
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</p>
+
<br>
 
[[File:T--Thessaly--GB-AATG-GCTT.jpeg|700px|thumb|none|<i><b>Fig.3:</b>The overhangs of this part in the Golden Braid Grammar</i>]]
 
[[File:T--Thessaly--GB-AATG-GCTT.jpeg|700px|thumb|none|<i><b>Fig.3:</b>The overhangs of this part in the Golden Braid Grammar</i>]]
  

Revision as of 10:34, 26 October 2020


sfGFP GB compatible with B3-B5


Level 0 sfGFP

Fig.1:sfGFP


Fig.2:sfGFP uder control of pTRC

Usage and Biology

A reporter gene fluorescent protein

  • Excitation at 485 nm
  • Emission at 510 nm


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 pUPD2 BBa_K3505007

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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 149
  • 1000
    COMPATIBLE WITH RFC[1000]