Difference between revisions of "Team:Saint Rose School A/Results"

 
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"><strong>July 8rd:<strong> our samples failed to be clear.
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"><strong>July 8th:</strong> our samples failed to be clear.
 
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"><strong> July 22nd:</strong> Too heated, without result.
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<img src="https://static.igem.org/mediawiki/2016/9/9b/Result2igem.jpg">
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"><strong> July 22nd:</strong> the sample was too heated again, and we did not abtained any result.
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<img src="https://static.igem.org/mediawiki/2016/e/e9/Result3igem.jpg">
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"><strong> July 23rd:</strong> performed in a small chamber gel 1.5, with Plux promoter, we weren´t able to see the two bands as espected..
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"><strong> July 30th:</strong> No result was obtained from all samples, it will be repeated.
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"><strong> August 5th:</strong> the expected samples could be clearly seen, the third tends to have two bands.
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"><strong> August 10th:</strong> plasmids concentrates, all the samples were completely able to be seen, getting the expected result.
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"><strong> August 12th: </strong>we turned to repeat samples to make sure everything is correct, then the plasmids were sent to cryogenics.
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Latest revision as of 01:14, 20 October 2016


Results

After carrying out laboratory work, the way we used to check if our work was successful was through electrophoresis using agarose gel 0.8; 1.2 and 1.5 depending on its need. 
Our laboratory work began in June this year and since then, we have been working. Now, we will see our performance in Lux:

July 8th: our samples failed to be clear.

July 22nd: Too heated, without result.

July 22nd: the sample was too heated again, and we did not abtained any result.

July 23rd: performed in a small chamber gel 1.5, with Plux promoter, we weren´t able to see the two bands as espected..

July 30th: No result was obtained from all samples, it will be repeated.

August 5th: the expected samples could be clearly seen, the third tends to have two bands.

August 10th: plasmids concentrates, all the samples were completely able to be seen, getting the expected result.

August 12th: we turned to repeat samples to make sure everything is correct, then the plasmids were sent to cryogenics.