Team:UNICAMP-Brazil/Notebooks/September 4
From 2009.igem.org
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*<p style=”text-align:justify;”> We tried again to amplify the hemolysin operon, but this time we reduced the annealing temperature to 50, 48, 46, 44, 42, 40 and 38 Celsius degrees. Again we do not had positive results. | *<p style=”text-align:justify;”> We tried again to amplify the hemolysin operon, but this time we reduced the annealing temperature to 50, 48, 46, 44, 42, 40 and 38 Celsius degrees. Again we do not had positive results. | ||
The DNA used was extracted from wild strains alpha hemolysin positive, we decided to use a already known strain, O26H-, which probably has the plasmidial hemolysin. | The DNA used was extracted from wild strains alpha hemolysin positive, we decided to use a already known strain, O26H-, which probably has the plasmidial hemolysin. | ||
- | Our primers was designed to plasmidial hemolysin and we don’t know if the wild strains have plasmidial or chromosomal hemolysin. | + | Our primers was designed to plasmidial hemolysin and we don’t know if the wild strains have plasmidial or chromosomal hemolysin.</p> |
''Marcos'' | ''Marcos'' | ||
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==''' ColiGuards '''== | ==''' ColiGuards '''== |
Revision as of 16:59, 20 October 2009
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