Difference between revisions of "Team:Dalhousie Halifax NS/Experiments"

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       <h4><a href="https://static.igem.org/mediawiki/2016/d/d6/T--Dalhousie_Halifax_NS--PowerFecalProtocol.pdf"> Decal Sample DNA Extraction </a></h4>
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       <h4><a href="https://static.igem.org/mediawiki/2016/d/d6/T--Dalhousie_Halifax_NS--PowerFecalProtocol.pdf"> Fecal Sample DNA Extraction </a></h4>
 
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     <p>To extract environmental DNA from fecal samples. This extraction will purify genomic DNA from prokaryotic and eukaryotic cells found in the fecal sample.  
 
     <p>To extract environmental DNA from fecal samples. This extraction will purify genomic DNA from prokaryotic and eukaryotic cells found in the fecal sample.  
 
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    <p><a href="https://static.igem.org/mediawiki/2016/7/70/T--Dalhousie_Halifax_NS--PowerFecalConcentration.pdf">MoBio DNA Extraction Protocol</a></p>
 
 
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       <h4> DNA Quantification </h4>
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       <h4><a href="https://static.igem.org/mediawiki/2016/7/70/T--Dalhousie_Halifax_NS--PowerFecalConcentration.pdf"> DNA Quantification </a></h4>
 
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Revision as of 12:18, 10 October 2016

Dalhousie iGEM 2016

Experiments


High Through-put Sequencing


To extract environmental DNA from fecal samples. This extraction will purify genomic DNA from prokaryotic and eukaryotic cells found in the fecal sample.

Concnetration protocol to concentrate DNA isolating using the PowerFecal Extraction kit.


DNA Extraction


Explanation of DNA Extraction here

MoBio DNA Extraction Protocol


Isolation of Bacteria


Congo Red Cellulose media can be used to isolate bacteria that degrade cellulose. It does this because the only carbon source in the media is cellulose. It uses Whatman Paper and gelatin.

Colony PCR has many applications including; verifying that an insert has been successfully incorporated in plasmid constructs, insert orientation, and species determination of unknown samples. The later was the reason for our use of Colony PCR. After streaking fecal sample onto cellulose plates, we picked colonies of different morphologies to find out which species or genus they were. We did this by using primers that targeted conserved sequence found in bacteria so we could amplify the DNA of almost all bacteria.

Instead of PCR clean up, we used ExoSap It. ExoSap It allows for an enzymatic clean-up of left over dNTPs and single stranded DNA. It is a very quick procedure as the only activation ExoSap It needs is a 15 minute 37°C incubation and a 15 minute 80 °C inactivation.