Difference between revisions of "Team:Munich/HP/Gold Integrated"

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<h3><a class="myLink" href="/Team:Munich/Gold_Integrated/KeithPardee123">Read part of the interview here...</a></h3>
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<h3><a class="myLink" href="/Team:Munich/Gold_Integrated/KeithPardee">Read part of the interview here...</a></h3>
 
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Revision as of 23:36, 28 October 2017

Description

Design

Demonstrate

Measurement

Applied Design

Final Results

Achievements

Protocols

Notebook

Safety

Parts

Improved Part

Part Collection

InterLab

Model

Software

Collaboration

Detector

Quake Valve

Paperstrips

Sample Processing

Silver

Gold

Engagement

Collaborations

Team members

Sponsors

Attributions

Gallery

Human Practices (Gold)

Collaborations play a very important role in terms of the development of project. Collaborations with other teams helps us to learn about better ways to handle a problem, to learn new ways of working, to perceive different ideologies and to develop the project in general. It provides us a better chance to get to know other teams and to learn to cooperate. In scientific fields, cooperation and collaborations play a major role for growth and discovery. We are highly encouraged to work with other teams since it increases our horizon of knowledge and we are happy that iGEM promotes the idea of sharing knowledge and scientific materials. The following are the teams whom we can proudly call the collaborators this year.

Interview with Dr. Keith Pardee

We had the chance to interview and talk with Dr. Keith Pardee on September 21th via Skype. He was impressed with our project and gave us very useful feedback. One of his suggestions was that we tried to make our device as easy as possible in the beginning and then get to the next level of complexity. For that reason, he suggested us to use first purified RNA that mimicked our target and at high concentrations, instead of considering using human samples. We followed his recommendations and could detect the 16S ribosomal subunit from Escherichia coli, from purified total RNA and in vitro RNA. When we asked him about our readout ideas (fluorescence and colorimetric), he told us that the fluorescent readout would be enough to prove that our device worked. Also, he recommended us to implement trehalose as a cryoprotectant in our method to lyophilize Cas13a into our paperstrip.

Read part of the interview here...

 Keith Pardee