Team:Technion/Attributions
From 2012.igem.org
Attributions
During our project we have used parts that were given to us by different labs or were taken from the registry/distribution kit.
Donated parts
- Ann K. Ganesan - WT T7 RNAP
- Changwon Kang - WT SP6 RNAP
- Christopher A. Voight - T7*, T7*(T3), T7*(N4), T7*(K1F) RNAPs with suitable induced promoters: pT7, pT3, pK1F, pN4
- Gallivan Lab (Gallivan Justin P., Lynch Sean A.) - Theophylline riboswitch and pTAC
- Roee's Lab (Roee Amit) - Cerulean FP under control of pLac/Ara, mCitrin FP and mCherry under control of pTetO.
Parts from Distribution Kit
Name | Description | BBa_B0015 | Double terminator | BBa_F2620 | TetR controllable LuxR and lux pR genes | BBa_I0462** | LuxR protein generator | BBa_I13522** | GFP under pTetO control | BBa_J06504** | mCherry FP | BBa_J06702 | mCherry, bacterial with RBS and forward terminator | BBa_J23119 | Constitutive promoter | BBa_R0062 | Promoter (luxR & HSL regulated -- lux pR) | pSB1C3 | High copy BioBrick assembly plasmid | pSB3C5 | Low to medium copy BioBrick standard vector |
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Notes: Parts followed by ** are parts that haven't worked because distribution kit contained some other DNA in the well where the part should be.
Contributions
- We have submitted 25 BioBricks to the registry. Due to lack of time we haven't managed to put all the parts inside the shipping plasmid.
- We have managed to successfully clone 4 out of 8 parts that phage's genome had been divided into.
- We have creatednew reporter system to test our YES gates and hope that it will become standard system for testing other parts as well. We used it to characterize T7 RNAP activity, the results can be seen here.