Difference between revisions of "Team:Freiburg/Home"
Line 13: | Line 13: | ||
color: #000000; | color: #000000; | ||
font: "Roboto"; | font: "Roboto"; | ||
− | + | font-weight: 400; | |
− | + | font-size: 25px; | |
} | } | ||
.homepage_text{ | .homepage_text{ | ||
+ | padding-top:20px; | ||
color:#000000; | color:#000000; | ||
font-weight: thin; | font-weight: thin; | ||
text-align: center; | text-align: center; | ||
} | } | ||
− | |||
− | |||
− | |||
#what_box, #how_box, #why_box{ | #what_box, #how_box, #why_box{ | ||
+ | box-sizing:border-box; | ||
clear:both; | clear:both; | ||
position: relative; | position: relative; | ||
Line 37: | Line 36: | ||
} | } | ||
− | |||
− | |||
− | |||
− | |||
Line 48: | Line 43: | ||
#what_left{ | #what_left{ | ||
+ | } | ||
+ | #what_diachip_logo{ | ||
+ | padding-left: 50px; | ||
} | } | ||
#what_right{} | #what_right{} | ||
Line 64: | Line 62: | ||
} | } | ||
#how_right{ | #how_right{ | ||
− | + | padding-top:25px; | |
} | } | ||
Line 79: | Line 77: | ||
} | } | ||
#why_left{} | #why_left{} | ||
− | #why_right{ | + | |
− | width:326px; | + | #why_right { |
+ | padding-right: 90px; | ||
+ | width: 326px; | ||
+ | padding-top: 30px; | ||
} | } | ||
+ | |||
#why_image img{ | #why_image img{ | ||
+ | |||
width:326px; | width:326px; | ||
} | } |
Revision as of 23:07, 3 September 2015
![](https://static.igem.org/mediawiki/2015/8/85/Freiburg_wiki_background_2_parted_left.png)
![](https://static.igem.org/mediawiki/2015/f/f4/Freiburg_wiki_background_2_parted_right.png)
![](https://static.igem.org/mediawiki/2015/9/91/Freiburg_homepage_Dia_chip.png)
![](https://static.igem.org/mediawiki/2015/0/0f/Freiburg_homepage_chip_blood.png)
![](https://static.igem.org/mediawiki/2015/b/b6/Freiburg_homepage_chip_denature.png)
Abstract
In modern medicine, fast detection and differentiation of diseases is a crucial and fundamental task. Typical ELISA-based assays are time-consuming and expensive. We propose an advanced procedure for the simultaneous detection of various diseases in a fast and inexpensive manner, the DiaCHIP. Our approach is based on the interaction of antibodies with their respective antigens. Different antigens are immobilized on a protein array generated by cell-free protein expression, using the corresponding DNA array as a template. Placed in a microfluidic chamber, the protein array is incubated with a patient’s blood sample. The interaction between an antibody in the sample and the corresponding immobilized antigen results in a local change of the optical thickness of the surface. This change can be detected using a label-free and real-time measurement technology called iRIf (imaging Reflectometric Interference)which is based on a laser detecting the interference of reflecting light from our chip. Offering simultaneous screening for several diseases, our DiaCHIP has strong potential to improve future diagnostics.