Difference between revisions of "Team:Freiburg/Project/Overview"
| Line 374: | Line 374: | ||
<div class="artboard"> | <div class="artboard"> | ||
<div class="sliderimage"> | <div class="sliderimage"> | ||
| − | |||
<div class="dummy-image"></div> | <div class="dummy-image"></div> | ||
</div> | </div> | ||
| Line 382: | Line 381: | ||
</div> | </div> | ||
<div class="slidertext indent"> | <div class="slidertext indent"> | ||
| − | <p> | + | <p> Praesent et diam eget libero egestas mattis sit amet vitae augue. <br> Want to read <a href="https://2015.igem.org/Team:Freiburg/OwnDevice"> more?</a> |
</p> | </p> | ||
</div> | </div> | ||
| Line 390: | Line 389: | ||
<div class="artboard"> | <div class="artboard"> | ||
<div class="sliderimage"> | <div class="sliderimage"> | ||
| − | |||
<div class="dummy-image"></div> | <div class="dummy-image"></div> | ||
| − | |||
</div> | </div> | ||
<div class="slidertext"> | <div class="slidertext"> | ||
| Line 399: | Line 396: | ||
</div> | </div> | ||
<div class="slidertext indent"> | <div class="slidertext indent"> | ||
| − | <p> | + | <p> Praesent et diam eget libero egestas mattis sit amet vitae augue. <br> Want to read <a href="https://2015.igem.org/Team:Freiburg/Practices"> more?</a></p> |
</div> | </div> | ||
</div> | </div> | ||
| Line 406: | Line 403: | ||
<div class="artboard"> | <div class="artboard"> | ||
<div class="sliderimage"> | <div class="sliderimage"> | ||
| − | |||
<div class="dummy-image"></div> | <div class="dummy-image"></div> | ||
| − | |||
</div> | </div> | ||
<div class="slidertext"> | <div class="slidertext"> | ||
| Line 415: | Line 410: | ||
</div> | </div> | ||
<div class="slidertext indent"> | <div class="slidertext indent"> | ||
| − | <p> | + | <p> Praesent et diam eget libero egestas mattis sit amet vitae augue. <br> Want to read <a href="https://2015.igem.org/Team:Freiburg/Modeling">more?</a> </p> |
</div> | </div> | ||
</div> | </div> | ||
| Line 422: | Line 417: | ||
<div class="artboard"> | <div class="artboard"> | ||
<div class="sliderimage"> | <div class="sliderimage"> | ||
| − | |||
<div class="dummy-image"></div> | <div class="dummy-image"></div> | ||
| − | |||
</div> | </div> | ||
<div class="slidertext"> | <div class="slidertext"> | ||
| Line 431: | Line 424: | ||
</div> | </div> | ||
<div class="slidertext indent"> | <div class="slidertext indent"> | ||
| − | <p> | + | <p> Praesent et diam eget libero egestas mattis sit amet vitae augue. <br> Want to read <a href="https://2015.igem.org/Team:Freiburg/Results">more?</a></p> |
</div> | </div> | ||
</div> | </div> | ||
Revision as of 14:12, 5 September 2015
Project overview: The DiaCHIP
The DiaCHIP is a new tool to simultaneously detect antibodies corresponding to different diseases in blood sera. It may greatly simplify broad band screenings, detection of autoimmune diseases and determination of vaccination status. Essential for our project idea is the combination of protein synthesis directly in the diagnostic device using a new and label-free detection system so simple that it can easily be rebuild by future iGEM teams.
Preparing the DiaCHIP
As the DiaCHIP relies on antibody-antigen interactions, the antigens first have to be synthesized and immobilized inside the device. Given that the whole device is a microfluidic system, it was most convenient to do this directly in the flow-chamber, where detection will finally take place. The flow-chamber consists of two surfaces separated by a gap that can be flushed with liquids. On the one surface DNA molecules providing the information for the antigens are attached and can be transcribed and translated into protein when a cell-free expression mix is flushed through the chamber. Proteins then diffuse until reaching the second surface that specifically captures the proteins encoded by the immobilized DNA. After several washing steps to remove remaining expression-mix the flow-chamber is coated with antigens and ready for detection.
Measuring
With the iRIf system it is possible to record small changes in layer thickness. The binding of an antibody from the blood serum flushed through the chamber to the according antigen increases the thickness of the protein surface so that interaction events can be measured label-free and in real-time.
But we didn't stop thinking about the device: We detected antibodies in our own blood!
