Team:Tuebingen/Notebook/Protocols
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<h1>Protocols</h1> | <h1>Protocols</h1> | ||
- | < | + | <ul> |
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/competent_cells">Creating competent <i>Escherichia coli</i> cells</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/gelelectrophoresis">Agarose gel electrophoresis</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/gelextraction">Agarose gel extraction</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/ligation">DNA-Ligation</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/laemmli">Laemmli buffer</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/LB_agar">LB agar</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/LB_medium">LB medium</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/LB_plates">LB plates</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/loading_buffer">Loading buffer</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/MALDI">MALDI mass spectrometry analysis</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/mutagenesis_PCR">Mutagenesis PCR</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/Ni_NTA_Buffers">Ni NTA buffers</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/NiNTA">Ni NTA purification</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/OligoAnnealing">Oligo Annealing</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/PCR">PCR</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/SyntheticPeptides">Peptidesynthesis</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/miniprep">Preparation of plasmids on a small scale</li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/restriction">Preparative restriction digests of BioBricks and plasmids </a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/SDS-PAGE">SDS-PAGE</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/TAE_buffer">TAE buffer</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/TBE_buffer">TBE buffer</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/3A_assembly">Three part assembly</a></li> | ||
+ | <li><a href="/Team:Tuebingen/Notebook/Protocols/transformation">Transformation of <i>E. coli</i></a></li> | ||
+ | </ul> | ||
+ | |||
</div> | </div> |
Latest revision as of 01:22, 18 October 2014
Protocols
- Creating competent Escherichia coli cells
- Agarose gel electrophoresis
- Agarose gel extraction
- DNA-Ligation
- Laemmli buffer
- LB agar
- LB medium
- LB plates
- Loading buffer
- MALDI mass spectrometry analysis
- Mutagenesis PCR
- Ni NTA buffers
- Ni NTA purification
- Oligo Annealing
- PCR
- Peptidesynthesis
- Preparation of plasmids on a small scale
- Preparative restriction digests of BioBricks and plasmids
- SDS-PAGE
- TAE buffer
- TBE buffer
- Three part assembly
- Transformation of E. coli