IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/08/21: Difference between revisions
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==Floor One== | |||
Made 6 x 500 ml SFM agar, autoclaved for 1 hr and poured into plates (only 3 x 500 ml had 500 ul Nystatin added). | |||
Performed 24 spore stocks of lawns - filtered, concentrated and resuspended spores in 20 % glycerol. | |||
Looked at spore titres. A total of 13 of the 15 spore stocks titred had the minimum required for succesful Bioassay of 10^-8 spores. | |||
==Floor Two== | ==Floor Two== | ||
Minipreps of BL21 containing pETAntA and AntGp+RFP plasmids were prepared using 5ml from each overnight culture and incubated with PstI restriction enzyme for analysis by gel electrophoresis. We also prepared the biobrick BBa_K1041000 (sample 3b2) by cutting with restriction enzyme NdeI and analysing on an agarose gel. The large fragment was cut from the gel to be purified. This process should remove the extra NdeI sites that were introduced to the sequence.<br> | Minipreps of BL21 containing pETAntA and AntGp+RFP plasmids were prepared using 5ml from each overnight culture and incubated with PstI restriction enzyme for analysis by gel electrophoresis. We also prepared the biobrick BBa_K1041000 (sample 3b2) by cutting with restriction enzyme NdeI and analysing on an agarose gel. The large fragment was cut from the gel to be purified. This process should remove the extra NdeI sites that were introduced to the sequence.<br> | ||
Revision as of 08:05, 22 August 2013
 Week Twelve
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Floor OneMade 6 x 500 ml SFM agar, autoclaved for 1 hr and poured into plates (only 3 x 500 ml had 500 ul Nystatin added). Performed 24 spore stocks of lawns - filtered, concentrated and resuspended spores in 20 % glycerol. Looked at spore titres. A total of 13 of the 15 spore stocks titred had the minimum required for succesful Bioassay of 10^-8 spores.
Floor TwoMinipreps of BL21 containing pETAntA and AntGp+RFP plasmids were prepared using 5ml from each overnight culture and incubated with PstI restriction enzyme for analysis by gel electrophoresis. We also prepared the biobrick BBa_K1041000 (sample 3b2) by cutting with restriction enzyme NdeI and analysing on an agarose gel. The large fragment was cut from the gel to be purified. This process should remove the extra NdeI sites that were introduced to the sequence.  100μL from two of the overnight cultures was used to inoculate two fresh 10ml LB with added antibiotics Kanamycin and Chlorophenicol. They were incubated for 2 hours at 37°C and then one culture was induced with IPTG. OutreachWe began designing the Outreach registry on our wiki pages.
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