Imperial College/10 August 2008
From 2008.igem.org
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Team members - James and Krupa + more if work load is too much. | Team members - James and Krupa + more if work load is too much. | ||
- | + | =====Monday===== | |
*Prepare an overnight culture of DL1-blue ''E.coli'' with the pDR110 integration vector, | *Prepare an overnight culture of DL1-blue ''E.coli'' with the pDR110 integration vector, | ||
*Prepare an 2x overnight culture of ''B.subtilis'', | *Prepare an 2x overnight culture of ''B.subtilis'', | ||
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*Design all primers for PCR cloning | *Design all primers for PCR cloning | ||
- | + | =====Tuesday===== | |
*Transform XL1-blue ''E.coli'' with Biobricks containing BBa_B0015, BBa_C0012 and pSB1A3 | *Transform XL1-blue ''E.coli'' with Biobricks containing BBa_B0015, BBa_C0012 and pSB1A3 | ||
- | + | =====Wednesday to Friday===== | |
*PCR clone AmyE from pDR111 and XylR from the ''B.subtilis'' genome when primers arrive | *PCR clone AmyE from pDR111 and XylR from the ''B.subtilis'' genome when primers arrive |
Revision as of 20:32, 28 October 2008
10 August 2008Wetlab TeamB.subtilisTeam members - James and Krupa + more if work load is too much. Monday
Tuesday
Wednesday
Thursday
Friday
Produce cell number against OD600nm calibration curve for use in characterisation Do we want to do this next week or the following week? A possible activity for Friday if Wednesday's transformation is found to have failed? CloningChris and Tom for this week Monday
Tuesday
Wednesday to Friday
Microscope
Drylab TeamEnd of week fiveFinish tutorial 2:
Next week
Thursday
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