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SEPTEMBER: WEEK 1
September, 2ndE3-1C3-2 was purified in order to screen the part length.
R0040 in J61002-1C3, E3N-1C3 and J101-31N-1C3 were transformed in 200 μl of TOP10 competent cells.
September, 3rd
All the cultures were diluted 1:200 in M9 with the proper antibiotic. After two hours T9002-ENTERO and ENTERO-RBS were aliquoted in 96-well microplate and induced with known concentrations of 3OC6-HSL and with the supernatants collected on August, 31st.
The sample did not show the correct band.
September, 4thR0040 in J61002-1C3-1, R0040 in J61002-1C3-2, J101-31-1C3-1 and J101-31-1C3-2 were glycerol stocked and then plasmidic DNA was purified with MiniPrep commercial kit:
2.5 μl of each sample were digested with 0.5 μl EcoRI and PstI resctriction endonucleases in a 25 μl final volume. A small size agarose gel was prepared. In the afternoon electrophoresis was carried out; all samples showed the correct insert.
Inoculum of T9002-ENTERO and ENTERO-RBS to measure 3OC6-HSL concentration in supernatants collected on August, 31st.
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Team:UNIPV-Pavia/Calendar/September/week1
From 2011.igem.org
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+ | <div class="center"><div class="thumb tnone"><div class="thumbinner" style="width: 550px;"><a href="/File:UNIPV_04_09_2011_R1_R2_J10131_1_J10131_2_EP.PNG" class="image"><img alt="" src="https://2011.igem.org/File:UNIPV_04_09_2011_R1_R2_J10131_1_J10131_2_EP.PNG" class="thumbimage" height="50%" width="50%"></a> <div class="thumbcaption">Small size gel</div></div></div></div> | ||
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Revision as of 14:22, 5 September 2011