Difference between revisions of "Team:UCL"

Line 48: Line 48:
 
     border-left-width: 0 !important;
 
     border-left-width: 0 !important;
 
}
 
}
@import url('https://fonts.googleapis.com/css?family=Orbitron');
+
/*@import url('https://fonts.googleapis.com/css?family=Orbitron');
@import url('https://fonts.googleapis.com/css?family=Josefin+Sans');
+
@import url('https://fonts.googleapis.com/css?family=Josefin+Sans');*/
 
@-webkit-keyframes pulse {
 
@-webkit-keyframes pulse {
 
     0% { box-shadow:0 0 8px #bfddf2, inset 0 0 8px #bfddf2; }
 
     0% { box-shadow:0 0 8px #bfddf2, inset 0 0 8px #bfddf2; }
Line 116: Line 116:
 
</style>
 
</style>
 
<head>
 
<head>
<link rel="stylesheet" type="text/css" href="https://2017.igem.org/Team:UCL/CSS">
+
<link rel="stylesheet" href="https://fonts.googleapis.com/css?family=Josefin+Sans"></link>
 +
    <link rel="stylesheet" href="https://fonts.googleapis.com/css?family=Orbitron"></link>
 +
    <link rel="stylesheet" type="text/css" href="mystyle.css">
 
     <script src="https://ajax.aspnetcdn.com/ajax/jQuery/jquery-3.2.1.min.js"></script>
 
     <script src="https://ajax.aspnetcdn.com/ajax/jQuery/jquery-3.2.1.min.js"></script>
 
     <link rel="stylesheet" href="https://maxcdn.bootstrapcdn.com/bootstrap/3.3.7/css/bootstrap.min.css"
 
     <link rel="stylesheet" href="https://maxcdn.bootstrapcdn.com/bootstrap/3.3.7/css/bootstrap.min.css"

Revision as of 11:06, 27 June 2017

LIT

Systems

Trying to reliably engineer cell structures?

Yes, we know it’s difficult.

How about adding some precision to targeting and controlling cellular mechanisms?

Our proposal is to design novel modular optogenetic control systems, with applications in a wide variety of areas, from tissue engineering to architecture. The project includes engineering of an immediate cell adhesion response using cell adhesion molecules and photoactivatable linkers for structure generation. Another application for our control system will be the production of a photoactivatable molecular tool for the precise activation of genes of interest. By targeting the genes for the transcription factors Oct3/4, Sox2, Klf4 and c-Myc we will also aim to create a novel mechanism for de-differentiation in mammalian cells. In the future, the precise spatiotemporal control of gene expression will enable reliable construction of any biological structure and sensor system.