Team:TU-Eindhoven/Wetlab

From 2013.igem.org

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<html><h1>Labwork Description</h1></html>
<html><h1>Labwork Description</h1></html>
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Within the scope of the 2013 iGEM competition our goal is to create tumor targeting bacteria which, upon the sensing of a tumor, would produce proteins that could be used for the imaging thereof. To achieve this, it is necessary to design and develop a system that targets and reacts to tumors, and is able to produce the proteins that enable the tumor imaging. In order to develop such a system, we first defined the [[ TU-Eindhoven/Preparation | '''DNA CONSTRUCTS''']] that constitute the basis of all our lab work. To ensure that the best possible protein was used for the tumor imaging it was decided to design and produce multiple different proteins. Once we generated our CEST contrast agent device, we tested the imaging qualities of the CEST contrast agent obtained by producing different proteins. The latter was done with an [[ TU-Eindhoven/MRIProcessing| '''MRI SCANNER''']]. We also evaluated the ability of our device to generate the contrast agent under hypoxic conditions by performing an [[ TU-Eindhoven/AnearobicTesting|'''ANAEROBIC TESTING''']] of the FNR Promoter.  
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Within the scope of the 2013 iGEM competition our goal was to create a bacterial tumor targeting device which, upon the sensing of a tumor, would produce proteins that could be used for the imaging thereof. To achieve this, it was necessary to design and develop a system that both targeted and reacted to tumors, producing the proteins that enable tumor imaging via MRI. In order to develop such a system, we first defined the [[ Team:TU-Eindhoven/Preparation | '''DNA CONSTRUCTS''']] that constitute the basis of all our lab work. To ensure that the best possible protein was used for the tumor imaging it was decided to design and produce multiple different proteins. Once able to generate a CEST contrast agent device, we [[ Team:TU-Eindhoven/CESTAgentTesting |'''TESTED THIS CONTRAST AGENT''']] by expressing each of the separate proteins and comparing their relative contrast. The measurement of the contrast produced by each of the proteins was done using an [[ Team:TU-Eindhoven/MRIProcessing | '''MRI SCANNER''']]. We also evaluated the ability of our device to generate a contrast agent under hypoxic conditions by performing an [[ Team:TU-Eindhoven/AnearobicTesting |'''ANAEROBIC TEST''']] with the FNR Promoter. The complete procedures and protocols performed during the lab work can be found on the [[ Team:TU-Eindhoven/LabJournal |'''LAB JOURNAL''']].
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The complete procedures and protocols that we performed within our lab work can be found on the [[ TU-Eindhoven/LabJournal|'''LAB JORUNAL''']].
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Latest revision as of 12:08, 26 October 2013

Labwork Description

Within the scope of the 2013 iGEM competition our goal was to create a bacterial tumor targeting device which, upon the sensing of a tumor, would produce proteins that could be used for the imaging thereof. To achieve this, it was necessary to design and develop a system that both targeted and reacted to tumors, producing the proteins that enable tumor imaging via MRI. In order to develop such a system, we first defined the DNA CONSTRUCTS that constitute the basis of all our lab work. To ensure that the best possible protein was used for the tumor imaging it was decided to design and produce multiple different proteins. Once able to generate a CEST contrast agent device, we TESTED THIS CONTRAST AGENT by expressing each of the separate proteins and comparing their relative contrast. The measurement of the contrast produced by each of the proteins was done using an MRI SCANNER. We also evaluated the ability of our device to generate a contrast agent under hypoxic conditions by performing an ANAEROBIC TEST with the FNR Promoter. The complete procedures and protocols performed during the lab work can be found on the LAB JOURNAL.