Difference between revisions of "Part:BBa K3505019"
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[[File:T--Thessaly--GB-AATG-GCTT.jpeg|700px|thumb|none|<i><b>Fig.2:</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.2:</b>The overhangs of this part in the Golden Braid Grammar</i>]] | ||
===Verification of cloning=== | ===Verification of cloning=== | ||
− | [[File:T--Thessaly--egfp0.png|600px|thumb|none|<i><b>Fig.3:</b>:</i>]] | + | [[File:T--Thessaly--egfp0.png|600px|thumb|none|<i><b>Fig.3:</b>:(U=Uncut C=Cut) Restriction digestion of EGFP (C1-C4 ) with : PvuII, Expected bands : 2826 bp , Positive Result : C4</i>]] |
===Experimental Use and Experience=== | ===Experimental Use and Experience=== |
Revision as of 15:05, 27 October 2020
eGFP GB compatible with B3-B5
Level 0 eGFP
Usage and Biology
- Derived from jellyfish Aequeora victoria
- A reporter gene fluorescent protein
- Excitation at 488 nm
- Emission at 515 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_K3505007and has overhangs compatible for Golden Braid cloning. The CDS has position B3-B5.
Verification of cloning
Experimental Use and Experience
This part is used in BBa_K3505029
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]