Difference between revisions of "Part:BBa K537011"
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| − | <p><big>For the pdf version of this datasheet, click <a href="https://static.igem.org/mediawiki/ | + | <p><big>For the pdf version of this datasheet, click <a href="https://static.igem.org/mediawiki/parts/2/27/Datasheet1.pdf">here</a></big></p> |
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Latest revision as of 19:37, 28 October 2011
Promoter-Theophylline riboswitch 1-CheZ-Venus-Double terminator
This composite BioBrick begins with a strong, constitutively active promoter of E.coli (BBa_J23119) followed by a theophylline riboswitch (type1) (Topp and Gallivan JACS 2007) which is fused to CheZ and Venus fluorescent reporter protein without stop codons in between. The Freiberg iGEM 2007 BioBrick 3.0 fusion protein assembly was used to construct this BioBrick. The theophylline riboswitch1-CheZ fusion was constructed via 2 rounds of PCR. This part ends with a standard double terminator transcriptional terminator for E.coli (BBa_B0015).
Note: All scar sites have been excluded in the annotations. There is a scar site between the Promoter:CheZ-Venus fusion and CheZ-Venus fusion:Double terminator. The scar sequence is as follows: ACTAGA
A Freiburg fusion scar site exists between the CheZ and Venus sequence. The sequence is as follows: ACCGGC
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1360
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
For the pdf version of this datasheet, click here
