"
Team:Calgary/Notebook/Protocols
From 2012.igem.org
(Difference between revisions)
| Line 37: | Line 37: | ||
<h2>Decatecholization</h2> | <h2>Decatecholization</h2> | ||
| - | <li><a href="https://2012.igem.org/Team:Calgary/Notebook/Protocols/decatecholization"> | + | <li><a href="https://2012.igem.org/Team:Calgary/Notebook/Protocols/decatecholization">Decatecholization (xylE and incubation with the Petrobrick)</a></li> |
<h2>Transposon</h2> | <h2>Transposon</h2> | ||
Revision as of 02:10, 2 October 2012
Hello! iGEM Calgary's wiki functions best with Javascript enabled, especially for mobile devices. We recommend that you enable Javascript on your device for the best wiki-viewing experience. Thanks!
Protocols
Here is a list of all the procedures we used this summer. Each contains a description and list of materials required.
- Agarose Gel Electrophresis
- Bacterial Genomic DNA Purification
- Bacterial Transformation
- Construction Techniques
- Gel Extraction
- LB Agar Plates
- Overnight Cultures
- PCR Purification
- Plasmid Purification (from E. coli)
- Preparing Chemically Competent Cells (E. coli)
- Preparing Glycerol Stocks (E. coli)
- Rehydration of Registry DNA
- Site-Directed Mutagenesis
- Taq PCR Protocol
Electrochemistry Protocols
- Electorchemistry protocols (include agarose bead making)
Desulfurization
- Desulphuirzation assay protocol
- Catalase/ hpac assays
Decarboxylation
- Petrobrick/oleT assay protocols/ GC MS
Denitrogenation
Decatecholization
- Decatecholization (xylE and incubation with the Petrobrick)
Transposon
Kill Switch
- Rhamnose, magnesium and manganese, kill gene assay (nuclease)
Bioreactor
- Bioreactor assays
Modeling
- Modelling validation experiments
