Imperial College/10 August 2008
From 2008.igem.org
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*Prepare an 2x overnight culture of ''B.subtilis'', | *Prepare an 2x overnight culture of ''B.subtilis'', | ||
*Prepare the reagents required for transformation, | *Prepare the reagents required for transformation, | ||
- | + | ======Tuesday====== | |
*Miniprep of the DL1-blye overnight culture, | *Miniprep of the DL1-blye overnight culture, | ||
*Make competent cells for both of the transformation protocols | *Make competent cells for both of the transformation protocols | ||
- | + | ======Wednesday====== | |
*Perform transformation of the competent cells using both protocols, | *Perform transformation of the competent cells using both protocols, | ||
- | + | ======Thursday====== | |
*Check successfulness of the transformation. If successful then perform transformation of linear DNA using previously made competent cells. | *Check successfulness of the transformation. If successful then perform transformation of linear DNA using previously made competent cells. | ||
- | + | ======Friday====== | |
*Check successfulness of the linear DNA transformation, | *Check successfulness of the linear DNA transformation, | ||
Revision as of 09:31, 8 August 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 Team
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