Difference between revisions of "Part:BBa K1157021:Experience"
Darlisereno (Talk | contribs) |
Darlisereno (Talk | contribs) |
||
| Line 5: | Line 5: | ||
===Applications of BBa_K1157021=== | ===Applications of BBa_K1157021=== | ||
This construct is a positive feedback circuit that expresses both C-4 AHL receptor RhlR and green fluorescence protein when AHL-binded RhlR combines to its promoter sequence. The design indicates that the promoter sequence is placed in front of the circuit, while the constitutive promoter is placed in the middle of the circuit. NYMU_Taipei assisted the functional testing by using ELISA plate reader to read GFP fluorescence intensity against C-4 AHL throughout time. The biosensor is cultured overnight and diluted until OD=0.1. We detect the fluorescence intensity from 0 to 4 hours. The results are as follows. | This construct is a positive feedback circuit that expresses both C-4 AHL receptor RhlR and green fluorescence protein when AHL-binded RhlR combines to its promoter sequence. The design indicates that the promoter sequence is placed in front of the circuit, while the constitutive promoter is placed in the middle of the circuit. NYMU_Taipei assisted the functional testing by using ELISA plate reader to read GFP fluorescence intensity against C-4 AHL throughout time. The biosensor is cultured overnight and diluted until OD=0.1. We detect the fluorescence intensity from 0 to 4 hours. The results are as follows. | ||
| − | [[File:Rhl positive feedback circuit.jpg| | + | [[File:Rhl positive feedback circuit.jpg|1000px]] |
===User Reviews=== | ===User Reviews=== | ||
Latest revision as of 15:14, 27 September 2013
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K1157021
This construct is a positive feedback circuit that expresses both C-4 AHL receptor RhlR and green fluorescence protein when AHL-binded RhlR combines to its promoter sequence. The design indicates that the promoter sequence is placed in front of the circuit, while the constitutive promoter is placed in the middle of the circuit. NYMU_Taipei assisted the functional testing by using ELISA plate reader to read GFP fluorescence intensity against C-4 AHL throughout time. The biosensor is cultured overnight and diluted until OD=0.1. We detect the fluorescence intensity from 0 to 4 hours. The results are as follows.
User Reviews
UNIQ6bcbd5541ac595e4-partinfo-00000000-QINU UNIQ6bcbd5541ac595e4-partinfo-00000001-QINU