Team:Newcastle/Parts
Alternative Roots
Parts Overview
Here we list the parts used in our study - both new and existing.
Parts Used
| Name | Type | Description | Designer | Length(bp) |
|---|---|---|---|---|
| BBa_I20270 | Coding sequence | Positive control for the interLab study | Jason Kelly | 919 |
| BBa_J364000 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_J364001 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_J364002 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_J364007 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_J364008 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_J364009 | Coding sequence | GFP gene for the interlab study | Traci Haddock-Angelli | 918 |
| BBa_R0040 | Regulatory sequence | TetR repressible promoter for the interlab study | June Rhee, Connie Tao, Ty Thomson, Louis Waldman | 54 |
| BBa_J04450 | Coding sequence | RFP gene for the interlab study | Tamar Odle | 1069 |
| BBa_K1033001 | Coding sequence | Catalyses the reaction from p-coumaric acid to 4-coumaroyl-coenzyme A | Karl Holdar | 1708 |
| BBa_K2797014 | Coding sequence | Catalyses the formation of p-coumaric acid from tyrosine | Heather Bottomley | 1596 |
| BBa_K1497000 | Coding sequence | Catalyses the reaction from naringenin chalcone to naringenin. | Sascha Hein, Niklas Hummel, Sebastian Barthel, Thomas Dohmen | 726 |
| BBa_K1497001 | Coding sequence | Catalyses the reaction from 4-Coumaroyl-CoA to naringenin chalcone. | Sascha Hein, Niklas Hummel, Sebastian Barthel, Thomas Dohmen | 1197 |
| BBa_K2797002 | Composite | Composite part for streptomycin resistance | Frank Eardley | 908 |
| BBa_K2797003 | Basic | mNeonGreen fluorescent protein gene codon optimised for expression in E. coli | Kyle Stanforth | 711 |
| BBa_K2797004 | Composite | Test device 1 (originally BBa_J364000) of the iGEM 2018 InterLab study with mNeonGreen replacing the GFPmut3b fluorescent reporter | Kyle Stanforth | 909 |
| BBa_K2797005 | Composite | Test device 2 (originally BBa_J364001) of the iGEM 2018 InterLab study with mNeonGreen replacing the GFPmut3b fluorescent reporter | Kyle Stanforth | 909 |
| BBa_K2797006 | Composite | Test device 3 (originally BBa_J364002) of the iGEM 2018 InterLab study with mNeonGreen replacing the GFPmut3b fluorescent reporter | Kyle Stanforth | 909 |
| BBa_K2797007 | Composite | Test device 4 (originally BBa_J364007) of the iGEM 2018 InterLab study with mNeonGreen replacing the GFPmut3b fluorescent reporter | Kyle Stanforth | 909 |
| BBa_K2797008 | Composite | Positive control (originally BBa_I20270) of the iGEM 2018 InterLab study with mNeonGreen replacing the GFPmut3b fluorescent reporter | Kyle Stanforth | 910 |
| BBa_K2797013 | Plasmid vector | High copy BioBrick assembly plasmid pSB1C3 with RFP internal standard | Kyle Stanforth | 3073 |
References & Attributions
Attributions: Frank Eardley, Heather Bottomley and Kyle Stanforth