Difference between revisions of "Part:BBa K1642010:Experience"

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===Applications of BBa_K1642010===
 
===Applications of BBa_K1642010===
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[[Image:SJTUB_PcpcG2-HR A.png|400px|left|Figure2. Biodesalination assay of the process controlled by PcpcG2.]]
 
The effectiveness of this biodesalinaion process is proved by determination of the concentrations of extracelluar sodium and chloride or desalination assay, which are shown in Figure 3. During the early time of working stage, there is an obvious decrease of concentration compared to that of Wild-type, which indicates that our biobrick (PcpcG2-HR, BBa_K1642010) really works in cyanobacteria under this biodesalination process! The following rise of concentration can be explained by the regain of energy under natural light in the working stage. Considering that we focus on the biodesalination process controlled by Pdark, we didn’t optimize this process.
 
The effectiveness of this biodesalinaion process is proved by determination of the concentrations of extracelluar sodium and chloride or desalination assay, which are shown in Figure 3. During the early time of working stage, there is an obvious decrease of concentration compared to that of Wild-type, which indicates that our biobrick (PcpcG2-HR, BBa_K1642010) really works in cyanobacteria under this biodesalination process! The following rise of concentration can be explained by the regain of energy under natural light in the working stage. Considering that we focus on the biodesalination process controlled by Pdark, we didn’t optimize this process.
<center>{{ Template:SJTU-BioX-Shanghai/Figure
 
| figure = [[File:SJTUB biode(41).jpg| 410px | frameless ]]
 
| float = middle
 
| id = 1.4.4
 
| label = Biodesalination assay of the process controlled by PcpcG2.
 
| descr = The start of induction stage is at -12h and the times of taking samples are at -12h, 4h, 12h and 24h.
 
}}</center>
 
  
 
===User Reviews===
 
===User Reviews===

Revision as of 21:51, 18 September 2015

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Applications of BBa_K1642010

Figure2. Biodesalination assay of the process controlled by PcpcG2.

The effectiveness of this biodesalinaion process is proved by determination of the concentrations of extracelluar sodium and chloride or desalination assay, which are shown in Figure 3. During the early time of working stage, there is an obvious decrease of concentration compared to that of Wild-type, which indicates that our biobrick (PcpcG2-HR, BBa_K1642010) really works in cyanobacteria under this biodesalination process! The following rise of concentration can be explained by the regain of energy under natural light in the working stage. Considering that we focus on the biodesalination process controlled by Pdark, we didn’t optimize this process.

User Reviews

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