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Team:Wageningen UR/VLPs ProjectOverview
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== VLPs == | == VLPs == | ||
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| - | + | The Wageningen UR team 2012 will work on the modification of virus-like particles (VLPs) to make them interesting platforms for vaccine production and/or site specific drug delivery. VLPs are empty virus capsids, meaning that they do not contain any viral genome, proteins and epitopes, except for the coat proteins.Three different viruses were selected: Cowpea Chlorotic Mottle Virus, Hepatitis B Virus and Polerovirus. All of them bear much promise for their respective qualities. | |
| - | Three different viruses were selected: Cowpea Chlorotic Mottle Virus, Hepatitis B Virus and Polerovirus. All of them bear much promise for their respective qualities. | + | <br><br> |
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Detection of the VLPs will be done using Electron Microscopy (EM) and Dynamic Light Scattering(DLS). | Detection of the VLPs will be done using Electron Microscopy (EM) and Dynamic Light Scattering(DLS). | ||
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[[Team:Wageningen_UR/VLPs|Read more]] | [[Team:Wageningen_UR/VLPs|Read more]] | ||
Latest revision as of 10:00, 26 September 2012
VLPs
The Wageningen UR team 2012 will work on the modification of virus-like particles (VLPs) to make them interesting platforms for vaccine production and/or site specific drug delivery. VLPs are empty virus capsids, meaning that they do not contain any viral genome, proteins and epitopes, except for the coat proteins.Three different viruses were selected: Cowpea Chlorotic Mottle Virus, Hepatitis B Virus and Polerovirus. All of them bear much promise for their respective qualities.
Detection of the VLPs will be done using Electron Microscopy (EM) and Dynamic Light Scattering(DLS).
