Difference between revisions of "Team:BIT/MO1"

Line 82: Line 82:
  
  
</footer>
+
<div id="fh5co-blog">
<div id="fh5co-started">
+
  <div class="overlay"></div>
+
<div class="container">
+
  <div class="row animate-box">
+
<div class="col-md-8 col-md-offset-2 text-center fh5co-heading">
+
 
+
<div id="fh5co-blog">
+
 
<div class="container">
 
<div class="container">
 
<div class="row animate-box">
 
<div class="row animate-box">
Line 104: Line 97:
 
</div>
 
</div>
 
</div>
 
</div>
 +
 +
</footer>
 +
<div id="fh5co-started">
 +
  <div class="overlay"></div>
 +
<div class="container">
 +
  <div class="row animate-box">
 +
<div class="col-md-8 col-md-offset-2 text-center fh5co-heading">
 +
 +
  
 
<center><h2>Hire Us!</h2></center>
 
<center><h2>Hire Us!</h2></center>

Revision as of 19:33, 29 October 2017

Dsign - Minimal portfolio Bootstrap template

Model of Biosensor

Abstract:

As we all know, it is difficult to detect macromolecules with synthetic biological methods. The hardest problem is that it is difficult for macromolecules to enter the gene machine - cell body, that leads to follow-up work out of the question. For this problem, we propose a model that replaces the substance with another substance. Alpha-fetoprotein (AFP) is the substance that our project wants to detect, but alpha-fetoprotein is a macromolecule and is difficult to enter the body of engineering bacteria. So we use lysine, an easily detectable substance, to establish a mathematical relationship with our target concentration to detect the concentration of AFP indirectly.

If we can prove that the amount of lysine separated at different AFP concentrations is different, then we can prove that our project is feasible. At the same time the aim of our project is detection, if the lysine detection quantity has linear relationship with AFP concentration, then our project will have obvious advantages in detection.

Hire Us!

Facilis ipsum reprehenderit nemo molestias. Aut cum mollitia reprehenderit. Eos cumque dicta adipisci architecto culpa amet.

Contact Us