Team:Calgary/Notebook/Protocols
From 2011.igem.org
(Difference between revisions)
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<h2>Microalgae Protocols</h2> | <h2>Microalgae Protocols</h2> | ||
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process5">Preparation of Algal f2 Media</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process5">Preparation of Algal f2 Media</a></li> | ||
- | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process6">Glass Bead Algal | + | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process6">Glass Bead Algal Transformation</a></li> |
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process7">Chloroplast Isolation</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process7">Chloroplast Isolation</a></li> | ||
- | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process8">Nuclear DNA | + | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process8">Nuclear DNA Extraction from Algae</a></li> |
<h2>Pseudomonas Biotinylation Techniques</h2> | <h2>Pseudomonas Biotinylation Techniques</h2> | ||
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<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process10">PCR Purification</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process10">PCR Purification</a></li> | ||
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process11">Gel Extraction</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process11">Gel Extraction</a></li> | ||
- | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process12">Testing the LacI-LacZ I732901 | + | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process12">Testing the LacI-LacZ I732901 Gene</a></li> |
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process13">Bacterial Transformation</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process13">Bacterial Transformation</a></li> | ||
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process14">Rehydration of Registry DNA</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process14">Rehydration of Registry DNA</a></li> | ||
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<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process17">LB Agar Plates</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process17">LB Agar Plates</a></li> | ||
<li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process18">Overnight Cultures</a></li> | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process18">Overnight Cultures</a></li> | ||
- | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process19">Preparing | + | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process19">Preparing Chemically Competent Cells (<i>E. coli</i>)</a></li> |
- | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process20">Preparing | + | <li><a href="https://2011.igem.org/Team:Calgary/Notebook/Protocols/Process20">Preparing Glycerol Stocks (<i>E. coli</i>) |
</ul> | </ul> |
Revision as of 03:20, 29 September 2011
Protocols
Here is a list of all the procedures we used this summer. Each contains a description and list of materials required.
- Preparation of Algal f2 Media
- Glass Bead Algal Transformation
- Chloroplast Isolation
- Nuclear DNA Extraction from Algae
- Plasmid Isolation (from Pseudomonas spp.)
- Genomic DNA Isolation (from Pseudomonas spp.)
- Biotinylation/Immunoprecipitation of Naphthenic Acids
- Conjugation of E. coli plasmids to Pseudomonas spp..
- Electrode Plating
- Buffer Preparation
- Electrical Settings
- Testing For Oxidation
- Plasmid Isolation (from E. coli)
- RNA Extraction
- cDNA Synthesis
- Quantitative Real Time PCR
- Testing the pBAD-LacZ Construct
- Taq PCR Protocol
- PCR Purification
- Gel Extraction
- Testing the LacI-LacZ I732901 Gene
- Bacterial Transformation
- Rehydration of Registry DNA
- Construction Techniques
- Agarose Gel Electrophresis
- LB Agar Plates
- Overnight Cultures
- Preparing Chemically Competent Cells (E. coli)
- Preparing Glycerol Stocks (E. coli)