IGEM:IMPERIAL/2007/Experimental Design/Phase1/Results 1.2

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pT7 was found to not to work. Its fluorescence reading was negligibly higher than a normal cell culture, and hence our conclusion is that the gene construct is faulty. (This was tested by comparing the plasmid length after a restriction enzyme digest, and the bands did not tally with the theoretical version of the plasmid construct.)

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