Team:EPF-Lausanne/Notebook/June2011

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Friday, 1st of July 2011

Alina and Lilia did MITOMI on His-TetR expressed from linear template, it was loaded on chip in ITT expression mix. DNA was spotted on June 29 in different concentrations for both: consensus (tetO1) sequence and a random sequence ((-)control).


Images: Green fluorescence comes from green-lysine and red fluorescence comes from DNA (cy-5 labeled).

Although we don't observe much protein bound to the anti His-tag antibody, we can still see that it does bound TetO1 sequence and did not bind any (-)control sequence. Some possible reasons for low protein fluorescence under the buttons: the expression yield from the linear template with T7 promoter might be too low, the His-tag to antibody binding is not strong enough or the concentration of antibody is too low.