IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/08/29: Difference between revisions
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==Floor One== | |||
Agarose gel electrophoresis showed that something had gone wrong during PCR - genomic DNA was visible.<br> | |||
A PCR reaction was repeated using 8 x 10 ul reactions of the same Master Mix proportions as before. A gradient PCR was performed this time where the annealing temperature was altered for each reaction in order to optimise the PCR.<br> | |||
Made 6 x 500 ml SFM (500 ul Ny per 500 ml). Autoclaved for 1 hr and poured into plates.<br> | |||
Made a 1% agarose gel.<br> | |||
Performed more spore stocks of lawned plates.<br> | |||
Diluted soil sample 85 to a concentration of 10^-4 and plated 100 ul of 10^-2 to 10^-4 dilutions on SFM + Ny agar plates.<br> | |||
==Floor Two== | ==Floor Two== | ||
As the agarose gel from the 22/08 was unsuccessful, the restriction digest of 3b and AntGpneo with PstI and NdeI was repeated. The miniprep BL21 cells that contain pETAntA and AntGpRFP plasmids were digested with XbaI. All samples were analysed by gel electrophoresis. <br> | As the agarose gel from the 22/08 was unsuccessful, the restriction digest of 3b and AntGpneo with PstI and NdeI was repeated. The miniprep BL21 cells that contain pETAntA and AntGpRFP plasmids were digested with XbaI. All samples were analysed by gel electrophoresis. <br> |
Revision as of 04:34, 3 September 2013
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Floor OneAgarose gel electrophoresis showed that something had gone wrong during PCR - genomic DNA was visible. Floor TwoAs the agarose gel from the 22/08 was unsuccessful, the restriction digest of 3b and AntGpneo with PstI and NdeI was repeated. The miniprep BL21 cells that contain pETAntA and AntGpRFP plasmids were digested with XbaI. All samples were analysed by gel electrophoresis.
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