Difference between revisions of "Team:Uppsala/Collaborations"
MatildaBrink (Talk | contribs) |
MatildaBrink (Talk | contribs) |
||
| Line 41: | Line 41: | ||
<div class="card-holder"> | <div class="card-holder"> | ||
<div class="content-card-heading"><h1>Bigass heading</h1> | <div class="content-card-heading"><h1>Bigass heading</h1> | ||
| − | <h2> | + | <h2></h2></div> |
<div class="content-card pic-next-to-text"> | <div class="content-card pic-next-to-text"> | ||
<div class="side-text"> | <div class="side-text"> | ||
Revision as of 14:53, 9 October 2018
During 2018, our team has collaborated with many other igem teams worldwide. Besides keeping close contact with all Nordic Teams through a common slack workspace for the project managers we have worked together in various other ways.
Vidilab
Bigass heading
From the start Vidilab has been a loyal partner; giving us not only informing us about the problem that needs solving but also with the equipment needed for RNA sequencing. In addition, they sponsored us with financial support in order to further the field of veterinary diagnostics.
Vidilab has throughout the summer been kind enough to provide us with fecal samples from a broad range of horses. This company has been a bridge between us and horse owners, giving us invaluable contacts and sharing our market analysis.
The header I want I put here
The text that I want will be here, in between these tags
Here is a second paragraph with E.coli written in italics. Any found genes which display promise will have to be validated by qPCR (which is a similar method) in a second run to confirm that they are only expressed due to the strongyle presence. Another approach to tackle our challenge is to screen for interaction between the surface proteins on the strongyle and short peptides. Through affinity screening of a random peptide library displayed on the surface of phages, we can select a peptide with a high affinity to the nematodes surface.