Difference between revisions of "Team:Freiburg/Home"
Line 7: | Line 7: | ||
<style> | <style> | ||
.content_box{ | .content_box{ | ||
− | |||
} | } | ||
Line 62: | Line 61: | ||
#how_left{ | #how_left{ | ||
− | + | width:400px; | |
} | } | ||
#how_right{ | #how_right{ | ||
Line 68: | Line 67: | ||
} | } | ||
− | + | #how_image{} | |
#how_image img{ | #how_image img{ | ||
− | width: | + | width:400px; |
} | } | ||
Line 77: | Line 76: | ||
#why_box{ | #why_box{ | ||
− | + | padding-top:300px; | |
+ | padding-bottom:100px; | ||
+ | } | ||
+ | #why_left{} | ||
+ | #why_right{ | ||
+ | width:326px; | ||
} | } | ||
#why_image img{ | #why_image img{ |
Revision as of 21:32, 3 September 2015
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.