Difference between revisions of "Team:Nankai/Parts"

 
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Latest revision as of 21:51, 18 September 2015

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Team Parts

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 ?

 

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