Difference between revisions of "Team:KCL UK/Safety"
| Line 2: | Line 2: | ||
<html> | <html> | ||
<head> | <head> | ||
| − | <link href="https:// | + | <link href="https://static.igem.org/mediawiki/2018/d/d7/T--KCL_UK--raleway.ttf" rel="stylesheet"> |
| + | |||
<meta charset="UTF-8"> | <meta charset="UTF-8"> | ||
<meta name="viewport" content="width= device-width, initial-scale=1"> | <meta name="viewport" content="width= device-width, initial-scale=1"> | ||
| Line 8: | Line 9: | ||
| − | <style> | + | <style> |
| + | |||
| + | @font-face { | ||
| + | font-family: "Raleway"; | ||
| + | src: url(https://static.igem.org/mediawiki/2018/d/d7/T--KCL_UK--raleway.ttf) format("truetype"); | ||
| + | } | ||
| + | |||
| + | |||
| + | |||
#top_title {display:none;} | #top_title {display:none;} | ||
| + | |||
| + | |||
| + | p { | ||
| + | font-family: 'Raleway', sans-serif; | ||
| + | display: block; | ||
| + | margin-top: 1em; | ||
| + | margin-bottom: 1em; | ||
| + | margin-left: 0; | ||
| + | margin-right: 0; | ||
| + | } | ||
| − | #content | + | #content, #HQ_page,h1 { |
animation : none; | animation : none; | ||
animation-delay : 0; | animation-delay : 0; | ||
| Line 162: | Line 181: | ||
z-index : auto; | z-index : auto; | ||
} | } | ||
| + | |||
| + | h1 { | ||
| + | font-family: 'Raleway', sans-serif; | ||
| + | display: block; | ||
| + | font-size: 2em; | ||
| + | margin-top: 0.67em; | ||
| + | margin-bottom: 0.67em; | ||
| + | margin-left: 0; | ||
| + | margin-right: 0; | ||
| + | font-weight: bold; | ||
| + | } | ||
a:hover {text-decoration:none;} | a:hover {text-decoration:none;} | ||
| Line 186: | Line 216: | ||
h1 { | h1 { | ||
font-family: 'Raleway', sans-serif; | font-family: 'Raleway', sans-serif; | ||
| + | |||
} | } | ||
Revision as of 20:41, 8 October 2018
what are we doing?
We are developing a new technology platform based on 3'UTR sequence characterisation to control soluble protein expression in E.coli.
We will use E.coli K12 to test our "Proof of Concept" Principle by engineering 3'UTR sequences (Sharma et al, 2011) to interact with either cytosolic proteins or 5'UTR sequences of our gene of interest: trxA and gor. Down regulation of these genes will be quantified by assessing quantitatively GFP signal. Efficiency of down regulation of genes will be quantified by assessing reaction kinetics of Alkaline Phosphatase (AP).
Some of Our Work
iGEM Symposium
See More
Bexley School Visit
See More
Social Media
See More
Lab Work
See More