Difference between revisions of "Team:Nankai/Parts"
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Revision as of 05:09, 18 September 2015
Parts Abstract
| Number | Name | Type | Description | Creator | Length |
|---|---|---|---|---|---|
| BBa_K1628001 | Pbca | Promoter | an original promoter of coding sequence pgsBCA operon | Tianyi Huang | 364 |
| BBa_K1628002 | Pxyl | Promoter | a promoter of xylose operon | Tianyi Huang | 217 |
| BBa_K1628003 | BJ27UP | Promoter | an artificially synthesized promoter | Xinhao Song | 100 |
| BBa_K1628004 | C2up | Promoter | an artificially synthesized promoter | Xinhao Song | 108 |
| BBa_K1628005 | A2up | Promoter | an artificially synthesized promoter | Yibing Wei | 107 |
| BBa_K1628006 | P43 | Promoter | a strong promoter in Bacillus subtilis 168 | Yibing Wei | 445 |
| BBa_K1628007 | PamyA | Promoter | a strong promoter in Bacillus amyloliquefaciens LL3 | Zhaoran Zhang | 613 |
| BBa_K1628101 | pgsB | Coding | a gene responsible for γ-PGA synthesis in pgsBCA operon | Tianyi Huang | 1182 |
| BBa_K1628102 | pgsCA | Coding | a coding gene in pgsBCA operon | Xinhao Song | 1631 |
| BBa_K1628201 | PlacI/lacI | Translational Unit | a promoter of lactose operon along with a repressor of lactose operon regulating the promoter | Yibing Wei | 1386 |
| BBa_K1628202 | Pgrac | Promoter | a promoter of lactose operon regulated by repressor LacI | Tianyi Huang | 120 |
| BBa_K1628203 | xylR | Coding | a repressor of xylose operon regulating promoter Pxyl | Zhaoran Zhang | 1167 |
| BBa_K1628301 | P1-GFP | Device | P3-GFP is a composite part used for the Measurement track of this year. This part consists of the promoter part of BBa_J23117, the official GFP device (with an RBS, GFP coding sequence and a set of double terminators) and a pSB1C3 backbone. We transformed this plasmid into E. coli cells and the fluorescence intensity of the GFP protein that was expressed by the bacteria was measured afterwards by a flow cytometry. | Tianyi Huang | ? |
| BBa_K1628202 | P2-GFP | Device | P2-GFP is a composite part used for the Measurement track of this year. This part consists of the promoter part of BBa_J23106, the official GFP device (with an RBS, GFP coding sequence and a set of double terminators) and a pSB1C3 backbone. We transformed this plasmid into E. coli cells and the fluorescence intensity of the GFP protein that was expressed by the bacteria was measured afterwards by a flow cytometry. | Xinhao Song | ? |
| BBa_K1628303 | P3-GFP | Device | P3-GFP is a composite part used for the Measurement track of this year. This part consists of the promoter part of BBa_J23117, the official GFP device (with an RBS, GFP coding sequence and a set of double terminators) and a pSB1C3 backbone. We transformed this plasmid into E. coli cells and the fluorescence intensity of the GFP protein that was expressed by the bacteria was measured afterwards by a flow cytometry. | Yibing Wei | ? |
