"
Team:Cambridge/Experiments
From 2011.igem.org
(Difference between revisions)
Felix Zhou (Talk | contribs) (→Main Project - 'Bactiridescence') |
Felix Zhou (Talk | contribs) (→Extraction of Genomic DNA for PCR) |
||
| Line 11: | Line 11: | ||
==Main Project - 'Bactiridescence'== | ==Main Project - 'Bactiridescence'== | ||
| - | === | + | ===[https://2011.igem.org/Team:Cambridge/Protocols/Extraction_of_genomic_DNA_from_squid|Extraction of Genomic DNA for PCR]=== |
Reflectin genes were amplified directly from [http://en.wikipedia.org/wiki/Loligo Loligo] tissue. Tissue from the Loligo genus was commercially available from fishing bait suppliers and culinary wholesalers. Primers were designed from the nucleotide sequences of three reflectin proteins identified in L. pealei, and used in a PCR reaction upon L. vulgaris genomic DNA. | Reflectin genes were amplified directly from [http://en.wikipedia.org/wiki/Loligo Loligo] tissue. Tissue from the Loligo genus was commercially available from fishing bait suppliers and culinary wholesalers. Primers were designed from the nucleotide sequences of three reflectin proteins identified in L. pealei, and used in a PCR reaction upon L. vulgaris genomic DNA. | ||
{{Template:Team:Cambridge/CAM_2011_TEMPLATE_FOOT}} | {{Template:Team:Cambridge/CAM_2011_TEMPLATE_FOOT}} | ||
Revision as of 10:00, 20 July 2011
Loading...
Contents |
Experiments
Details of the experiments carried out throughout the project are linked from this page. These experiments should also be linked to from the appropriate diary page.
Preliminary Exercise
Initial exercise during our 2 weeks crash course in synthetic biology with the aim of familiarising us with common laboratory methods of preparing and assembling DNA.
Main Project - 'Bactiridescence'
of Genomic DNA for PCR
Reflectin genes were amplified directly from Loligo tissue. Tissue from the Loligo genus was commercially available from fishing bait suppliers and culinary wholesalers. Primers were designed from the nucleotide sequences of three reflectin proteins identified in L. pealei, and used in a PCR reaction upon L. vulgaris genomic DNA.
