Difference between revisions of "IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/08/16"

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Latest revision as of 23:11, 26 September 2017

Igem-logo-150px.png Week Eleven Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png

Floor One

De-replicated single Streptomyces colony plates when it appeared that we had duplicates. This is spore stock the minimum amount of lawns.

Filtered, concentrated and resuspended spore stocks in 20 % glycerol.

Floor Two

The two overnight cultures, containing BL21 cells that had been transformed with Pet28AntA were retrieved. Culture 1a was used to make competent cells, while sample 1b was induced with IPTG and left to incubate at 25°C overnight. While the cells were growing, minipreps of BL21 PlySs and BL21 rosetta PlySs cultures were prepared and stored in the freezer.
The BL21 Pet28AntA competent cells were transformed with the biobrick BBa_K1041002 (AntG promoter + RFP gene) and spread onto a LB Agar plate containing Kanamycin and Chlorophenicol antibiotics and six control plates were prepared, fig 2

Fig 2: A table to show what each LB Agar plate contained.

Outreach

A meeting was held to discuss the upcoming forum event such as posters and layout for the tables.