Difference between revisions of "Team:China Tongji"
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− | <tr><td><h3 align="center" style="font-size:42px; color:teal"><b> Project Introduction </b></h3><br></td></tr> | + | <table width="90%" align="center"> <br> <tr><td><h3 align="center" style="font- |
+ | size:42px; color:teal"><b> Project Introduction </b></h3><br></td></tr> | ||
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− | <br> | + | <br> <p>In our project, we will use the technology of optogenetic and use light |
− | <p>In our project, we will use the technology of optogenetic and use light of defferent wave | + | of defferent wave produced by the special light source assembled by ourselves to |
− | produced by the special light source assembled by ourselves to control the moving of C.elegans, | + | control the moving of C.elegans, construct a movement controlling system and |
− | construct a movement controlling system and bulid an amusement park of C.elegans.</p> | + | bulid an amusement park of C.elegans.</p> <p>We will try to design our special |
− | <p>We will try to design our special parts and express channalrhodopsin in specific C.elegans' | + | parts and express channalrhodopsin in specific C.elegans' neurons. To accomplish |
− | neurons. To accomplish our goals to express channalrhodopsin in single neuron, we make the use of | + | our goals to express channalrhodopsin in single neuron, we make the use of cre- |
− | cre-loxp system and the overlapping of promoters. We not only use the traditional | + | loxp system and the overlapping of promoters. We not only use the traditional |
− | channalrhodopsin,chR2,but also try to express the novel channelrhodopsin, Blink, and other fancy | + | channalrhodopsin,chR2,but also try to express the novel channelrhodopsin, Blink, |
− | channelrhodopsins which have never been tested in C.elegans.</p> | + | and other fancy channelrhodopsins which have never been tested in C.elegans.</p> |
− | <p>And we will also get some parts and assemble those parts into a new equipment which can serves as | + | <p>And we will also get some parts and assemble those parts into a new equipment |
− | the light source of our experiment.Then we will use computer controlling that lightsource to | + | which can serves as the light source of our experiment.Then we will use computer |
− | change the light which can activate or suppress the channelrhodopsin. By doing that, we can try | + | controlling that lightsource to change the light which can activate or suppress |
− | to control the behaviours of C.elegans such as moving forwards or twisting more effectively.</p> | + | the channelrhodopsin. By doing that, we can try to control the behaviours of |
− | <p>What's more,we will express GFP,YFP,mcherry in E.coli and P.Aeruginosa. By combining the color of | + | C.elegans such as moving forwards or twisting more effectively.</p> <p>What's |
− | microorgasims and C.elegans, we want to construct some interesting scenes to form a C.elegans' | + | more,we will express GFP,YFP,mcherry in E.coli and P.Aeruginosa. By combining |
− | fancy world. </p> | + | the color of microorgasims and C.elegans, we want to construct some interesting |
− | <p>This technology will be helpful in the research on neuron's function and interaction. In the | + | scenes to form a C.elegans' fancy world. </p> <p>This technology will be helpful |
− | future, this technology may also be used in mechanical controlling system and the theraphy of | + | in the research on neuron's function and interaction. In the future, this |
− | movement defect. </p> | + | technology may also be used in mechanical controlling system and the theraphy of |
+ | movement defect. </p> <br> | ||
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Revision as of 08:59, 12 July 2015
Home | Project | Notebook | Achivement | Team | Outreach |
Project Introduction |
In our project, we will use the technology of optogenetic and use light of defferent wave produced by the special light source assembled by ourselves to control the moving of C.elegans, construct a movement controlling system and bulid an amusement park of C.elegans. We will try to design our special parts and express channalrhodopsin in specific C.elegans' neurons. To accomplish our goals to express channalrhodopsin in single neuron, we make the use of cre- loxp system and the overlapping of promoters. We not only use the traditional channalrhodopsin,chR2,but also try to express the novel channelrhodopsin, Blink, and other fancy channelrhodopsins which have never been tested in C.elegans. And we will also get some parts and assemble those parts into a new equipment which can serves as the light source of our experiment.Then we will use computer controlling that lightsource to change the light which can activate or suppress the channelrhodopsin. By doing that, we can try to control the behaviours of C.elegans such as moving forwards or twisting more effectively. What's more,we will express GFP,YFP,mcherry in E.coli and P.Aeruginosa. By combining the color of microorgasims and C.elegans, we want to construct some interesting scenes to form a C.elegans' fancy world. This technology will be helpful in the research on neuron's function and interaction. In the future, this technology may also be used in mechanical controlling system and the theraphy of movement defect. |