Team:UNICAMP-Brazil/Notebooks/September 15
From 2009.igem.org
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*<p style=”text-align:justify;”>We continued our work with finO and finP today by performing minipreps from yesterday's inoculated cultures, according to [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Mini-Prep Protocol 2].</p> | *<p style=”text-align:justify;”>We continued our work with finO and finP today by performing minipreps from yesterday's inoculated cultures, according to [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Mini-Prep Protocol 2].</p> | ||
*<p style=”text-align:justify;”>We had 10 cultures for finO and 10 cultures for finP, in order to assure that at least one of them would have the inserted fragment into it's plasmid.</p> | *<p style=”text-align:justify;”>We had 10 cultures for finO and 10 cultures for finP, in order to assure that at least one of them would have the inserted fragment into it's plasmid.</p> | ||
- | *<p style=”text-align:justify;”>It's important to highlight that a few samples showed a red coloration this morning. This could only be explained by the religation between the digested vector and it's part (RFP device). Yet we still decided to perform those samples's miniprep, we took note of those samples's numbers. | + | *<p style=”text-align:justify;”>It's important to highlight that a few samples showed a red coloration this morning. This could only be explained by the religation between the digested vector and it's part (RFP device). Yet we still decided to perform those samples's miniprep, we took note of those samples's numbers.</p> |
*<p style=”text-align:justify;”>After this procedure, we ran an agarose gel with all the samples, in order to check miniprep efficiency:</p> | *<p style=”text-align:justify;”>After this procedure, we ran an agarose gel with all the samples, in order to check miniprep efficiency:</p> | ||
Revision as of 16:22, 18 October 2009
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