Team:Wageningen UR/Protocol
From 2012.igem.org
(Difference between revisions)
MarkvanVeen (Talk | contribs) |
|||
(34 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | {{Template: | + | {{Template:WUR}} |
- | = | + | <html> |
+ | <script> | ||
+ | document.getElementById("header_slider").style.backgroundImage = "url(https://static.igem.org/mediawiki/2012/a/a3/HeaderNotebook.jpg)"; | ||
+ | </script> | ||
+ | </html> | ||
- | = | + | = Methods = |
- | + | The use of Virus-Like-Particles as medicine carrier is new for iGEM. This means the whole production, purification and detection of Virus-Like-Particles is also new in iGEM. In this section we will explain how the different methods work and how it all fits together. | |
- | + | ||
- | + | <ul> | |
- | + | <li>[[Team:Wageningen_UR/MethodsProduction|Production]]</li> | |
- | + | <li>[[Team:Wageningen_UR/MethodsPurification|Purification]]</li> | |
- | + | </ul> | |
+ | |||
+ | = Protocols = | ||
+ | |||
+ | == Medium & Buffer recipes == | ||
+ | |||
+ | <ul> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/LBmedium|LB medium]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/SOBmedium|SOB medium]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/SOCmedium|SOC medium]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Disassemblybuffer|Disassembly buffer]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Dialysisbuffer10x|Dialysis buffer 10x]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Reassemblybuffer|Reassembly buffer]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Virusbuffer|Virus buffer]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/FormationBufferHepB|Formation Buffer HepBcAg]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/WashingBuffer|Washing Buffer HepBcAg]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/FormationBufferPolero|Formation Buffer Polero]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Towbinselectrotransferbuffer1x|Towbin's electrotransfer buffer 1x]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Towbinselectrotransferbuffer10x|Towbin's electrotransfer buffer 10x]]</li> | ||
+ | </ul> | ||
== CCMV Coat Protein VLP formation == | == CCMV Coat Protein VLP formation == | ||
- | + | <ul> | |
- | + | <li>[[Team:Wageningen_UR/Protocol/StartupCCMV|Growing culture]]</li> | |
- | + | <li>[[Team:Wageningen_UR/Protocol/DialysisCCMV|Dialysis of the VLPs]]</li> | |
+ | <li>[[Team:Wageningen_UR/Protocol/RoundupCCMV|Purifying the VLPs]]</li> | ||
+ | </ul> | ||
== Hepatitis B Coat Protein VLP formation == | == Hepatitis B Coat Protein VLP formation == | ||
- | == | + | <ul> |
+ | <li>[[Team:Wageningen_UR/Protocol/StartupHepB|Growing culture]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/DialysisHepB|Dialysis of the VLPs]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/RoundupHepB|Purifying the VLPs]]</li> | ||
+ | </ul> | ||
+ | |||
+ | == Polerovirus Coat Protein VLP formation == | ||
+ | |||
+ | <ul> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/RNA|RNA isolation from potato leaf material]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/StartupPolero|Growing culture]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/DialysisPolero|Dialysis of the VLPs]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/RoundupPolero|Purifying the VLPs]]</li> | ||
+ | </ul> | ||
== General Protocol == | == General Protocol == | ||
+ | |||
+ | <ul> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/ElectrocompetentCells|Preparation of electrocompetent cells of ''E. coli'']]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/SDSPolyacrylamide|SDS-Polyacrylamide and native gel electrophoresis]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/DynamicLightScatteringMachine|Dynamic Light Scattering user manual]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Frenchpress|French press user manual]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/FPLC|FPLC user manual]]</li> | ||
+ | <li>[[Team:Wageningen_UR/Protocol/Mutagenesis|Mutagenesis]]</li> | ||
+ | </ul> |
Latest revision as of 10:44, 26 October 2012
Contents |
Methods
The use of Virus-Like-Particles as medicine carrier is new for iGEM. This means the whole production, purification and detection of Virus-Like-Particles is also new in iGEM. In this section we will explain how the different methods work and how it all fits together.
Protocols
Medium & Buffer recipes
- LB medium
- SOB medium
- SOC medium
- Disassembly buffer
- Dialysis buffer 10x
- Reassembly buffer
- Virus buffer
- Formation Buffer HepBcAg
- Washing Buffer HepBcAg
- Formation Buffer Polero
- Towbin's electrotransfer buffer 1x
- Towbin's electrotransfer buffer 10x
CCMV Coat Protein VLP formation
Hepatitis B Coat Protein VLP formation
Polerovirus Coat Protein VLP formation
General Protocol
- Preparation of electrocompetent cells of E. coli
- SDS-Polyacrylamide and native gel electrophoresis
- Dynamic Light Scattering user manual
- French press user manual
- FPLC user manual
- Mutagenesis