Team:BUCT-China/Project

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<tr><td height="41" > <h3> Project Description </h3></td>
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<p><span class="diego"><span class="diego"><span class="diego">Our project is based on genetic engineering to construct a recombinant plasmid and transform it into a host cell E.coli, given the comprehensive toxicity test ability and the function of the particular toxin detection. Use of microfluidic chips will accomplish a rapid detection of samples. Eventually, we will form a complete set of water quality toxin rapid detection system.
+
<p>Our project is based on genetic engineering to construct a recombinant plasmid and transform it into a host cell E.coli, given the comprehensive toxicity test ability and the function of the particular toxin detection. Using of microfluidic chips will accomplish a rapid detection of samples. Eventually, we will build a complete set of water quality toxin rapid detection system. </p>
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</span></span></span>
+
<p>The system is composed of a sampling device chip, lyophilized powder of recombinant strains and testing instruments. We use chips with recombinant bacteria to suck up the water samples, then put chips into the instrument. When the instrument works, we will acquire an automatic detection of physical and chemical characteristics of the samples after a period of time. And a test report is additional to show the final result. </p>
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<p><span class="diego"><span class="diego"><span class="diego">The system is compose of a sampling device chip, lyophilized power of recombinant strains and testing instruments. We use chips with recombinant bacteria to get the water samples, then put chips into the instrument. When the instrument works, we will acquire an automatic detection of physical and chemical characteristics of the samples after a period of time. And a test report is additional to show the final result.  
+
<p>The advantages of this system we believe are: Firstly, the recombinant host has strong resistance to toxin, providing a luminescent gene LuxAB in vivo and constructing a more stable platform for the expression of many biosensors. Secondly, microfluidic chips’ usage enhance the level of trace detection. Thirdly, inserted biosensors will completely accomplish the determination of one or several toxins, which can be taken as credible references to the comprehensive toxicity assessments. Multiple collocation of variable Biosensors also reflects the modular though modularization idea .</p>
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<p><span class="diego"><span class="diego"><span class="diego">The advantages of this system may be: Firstly, the recombinant host has strong resistance to toxin, providing a luminescent gene LuxAB in vivo and constructing a more stable platform for the expression of many biosensors. Secondly, microfluidic chips’ usage enhance the level of trace detection. Thirdly, inserted biosensors will completely accomplish the determination of one or several toxins, which can be taken as credible references to the comprehensive toxicity assessments. Multiple collocation of variable Biosensors also reflects the modular thought.</span></span>
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<h3>References </h3>
<h3>References </h3>
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<p> You can use these subtopics to further explain your project</p>
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</tr>
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<ol>
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<li>Overall project summary</li>
 +
<li>Project Details</li>
 +
<li>Materials and Methods</li>
 +
<li>The Experiments</li>
 +
<li>Results</li>
 +
<li>Data analysis</li>
 +
<li>Conclusions</li>
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</ol>
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<p>
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It's important for teams to describe all the creativity that goes into an iGEM project, along with all the great ideas your team will come up with over the course of your work.
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<h1 >WELCOME TO iGEM 2014! </h1>
 
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<p>Your team has been approved and you are ready to start the iGEM season!
 
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<br>On this page you can document your project, introduce your team members, document your progress <br> and share your iGEM experience with the rest of the world! </p>
 
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<br>
 
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<p style="color:#E7E7E7"> <a href="https://2014.igem.org/wiki/index.php?title=Team:BUCT-China/Project&action=edit"style="color:#FFFFFF"> Click here  to edit this page!</a> </p>
 
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<a href="https://2014.igem.org/Team:BUCT-China"style="color:#000000">Home </a> </td>
 
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<a href="https://2014.igem.org/Team:BUCT-China/Team"style="color:#000000"> Team </a> </td>
 
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<a href="https://igem.org/Team.cgi?year=2014&team_name=BUCT-China"style="color:#000000"> Official Team Profile </a></td>
 
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<a href="https://2014.igem.org/Team:BUCT-China/Project"style="color:#000000"> Project</a></td>
 
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<a href="https://2014.igem.org/Team:BUCT-China/Modeling"style="color:#000000"> Modeling</a></td>
 
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<a href="https://2014.igem.org/Team:BUCT-China/Notebook"style="color:#000000"> Notebook</a></td>
 
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<a href="https://2014.igem.org/Team:BUCT-China/Attributions"style="color:#000000"> Attributions </a></td>
 
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<td align ="center"> <a href="https://2014.igem.org/Main_Page"> <img src="https://static.igem.org/mediawiki/igem.org/6/60/Igemlogo_300px.png" width="55px"></a> </td>
 
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<!--Project content  -->
 
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<tr><td height="41" > <h3> Project Description </h3></td>
 
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<td width="2%" ></td >
 
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<td > <h3>&nbsp;</h3></td>
 
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</tr>
 
-
 
-
<tr>
 
-
<td width="97%"  valign="top">
 
-
<p><span class="diego"><span class="diego"><span class="diego">Our project is based on genetic engineering to construct a recombinant plasmid and transform it into a host cell E.coli, given the comprehensive toxicity test ability and the function of the particular toxin detection. Use of microfluidic chips will accomplish a rapid detection of samples. Eventually, we will form a complete set of water quality toxin rapid detection system.
 
-
</span></span></span>
 
-
<p><span class="diego"><span class="diego"><span class="diego">The system is compose of a sampling device chip, lyophilized power of recombinant strains and testing instruments. We use chips with recombinant bacteria to get the water samples, then put chips into the instrument. When the instrument works, we will acquire an automatic detection of physical and chemical characteristics of the samples after a period of time. And a test report is additional to show the final result.
 
-
</span>
 
-
</span>
 
-
</span>
 
-
<p><span class="diego"><span class="diego"><span class="diego">The advantages of this system may be: Firstly, the recombinant host has strong resistance to toxin, providing a luminescent gene LuxAB in vivo and constructing a more stable platform for the expression of many biosensors. Secondly, microfluidic chips’ usage enhance the level of trace detection. Thirdly, inserted biosensors will completely accomplish the determination of one or several toxins, which can be taken as credible references to the comprehensive toxicity assessments. Multiple collocation of variable Biosensors also reflects the modular thought.</span></span>
 
-
</span>
 
<p>
<p>
 +
It's also important to clearly describe your achievements so that judges will know what you tried to do and where you succeeded. Please write your project page such that what you achieved is easy to distinguish from what you attempted.
</p>
</p>
-
<br>
+
 
-
<h3>References </h3>
+
-
<p>
+
-
iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you. </p>
+
</td>
</td>
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<td></td>
 
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<td  width="1%"  valign="top">&nbsp;</td>
 
</tr>
</tr>

Latest revision as of 08:22, 13 August 2014

WELCOME TO iGEM 2014!

Your team has been approved and you are ready to start the iGEM season!
On this page you can document your project, introduce your team members, document your progress
and share your iGEM experience with the rest of the world!


Click here to edit this page!

Home Team Official Team Profile Project Parts Modeling Notebook Safety Attributions

Project Description

Content

Our project is based on genetic engineering to construct a recombinant plasmid and transform it into a host cell E.coli, given the comprehensive toxicity test ability and the function of the particular toxin detection. Using of microfluidic chips will accomplish a rapid detection of samples. Eventually, we will build a complete set of water quality toxin rapid detection system.

The system is composed of a sampling device chip, lyophilized powder of recombinant strains and testing instruments. We use chips with recombinant bacteria to suck up the water samples, then put chips into the instrument. When the instrument works, we will acquire an automatic detection of physical and chemical characteristics of the samples after a period of time. And a test report is additional to show the final result.

The advantages of this system we believe are: Firstly, the recombinant host has strong resistance to toxin, providing a luminescent gene LuxAB in vivo and constructing a more stable platform for the expression of many biosensors. Secondly, microfluidic chips’ usage enhance the level of trace detection. Thirdly, inserted biosensors will completely accomplish the determination of one or several toxins, which can be taken as credible references to the comprehensive toxicity assessments. Multiple collocation of variable Biosensors also reflects the modular though modularization idea .


References

iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you.

You can use these subtopics to further explain your project

  1. Overall project summary
  2. Project Details
  3. Materials and Methods
  4. The Experiments
  5. Results
  6. Data analysis
  7. Conclusions

It's important for teams to describe all the creativity that goes into an iGEM project, along with all the great ideas your team will come up with over the course of your work.

It's also important to clearly describe your achievements so that judges will know what you tried to do and where you succeeded. Please write your project page such that what you achieved is easy to distinguish from what you attempted.

Retrieved from "http://2014.igem.org/Team:BUCT-China/Project"