Team:UNICAMP-Brazil/Notebooks/September 14
From 2009.igem.org
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====Culture growth of bacteria containing the F plasmid==== | ====Culture growth of bacteria containing the F plasmid==== | ||
- | *<p style=”text-align:justify;”>From a permanent culture of bacteria | + | *<p style=”text-align:justify;”>From a permanent culture of bacteria containing the F plasmid, a sample was inoculated into liquid LB-AMP medium and let grow O/N at 37°C.</p> |
''Gabriel'' | ''Gabriel'' | ||
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====finO and finP's transformed bacteria==== | ====finO and finP's transformed bacteria==== | ||
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''Marcelo'' | ''Marcelo'' | ||
+ | ==== PY Promoter - Purification of the digestion reactions ==== | ||
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+ | *<p style=”text-align:justify;”>We purified the digestion reactions of PY1 and PY2 with the Invitrogen's PureLink™ PCR Purification Kit, following the manufacturer's protocol without modifications.</p> | ||
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+ | *<p style=”text-align:justify;”>We also prepared an agarose gel to run the digestion reaction of BBa_J23100. The band in the gel had the expected size (2940 bp). However, it is not possible to confirm the digestion by the size in the gel because the difference between the plasmid BBa_J23100 with and without the fragment excised by ''Xba''I and ''Spe''I is too small.</p> | ||
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+ | [[Image:py_gel_2.png|200px|center]] | ||
+ | *<p style=”text-align:justify;”>We excised the band from the gel and used the Invitrogen's PureLink™ Quick Gel Extraction Kit to perform the purification, following the manufacturer's protocol without modifications ([https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Purification_of_DNA_fragments_from_agarose_gels Protocol 7]).</p> | ||
+ | ''Fabi and Léo'' | ||
{{:Team:UNICAMP-Brazil/inc_rodape}} | {{:Team:UNICAMP-Brazil/inc_rodape}} |
Latest revision as of 02:35, 22 October 2009
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