"
Imperial College/10 August 2008
From 2008.igem.org
(Difference between revisions)
m |
m |
||
| Line 1: | Line 1: | ||
| - | + | ==WETLAB TEAM== | |
| - | + | ===''B.subtilis=== | |
| + | Begin culturing ''B.subtilis'' and transformation: | ||
*Monday | *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, | ||
| Line 15: | Line 16: | ||
**Check successfulness of the linear DNA transformation, | **Check successfulness of the linear DNA transformation, | ||
| + | Produce cell number against OD<sub>600nm</sub> calibration curve for use in characterisation<font color=red> Do we want to do this next week or the following week? </font> | ||
| + | |||
| + | |||
| + | ===Cloning=== | ||
#Transform XL1-blue ''E.coli'' with Biobricks containing BBa_B0015 and BBa_c0012 | #Transform XL1-blue ''E.coli'' with Biobricks containing BBa_B0015 and BBa_c0012 | ||
#Design all primers for PCR cloning | #Design all primers for PCR cloning | ||
#PCR clone AmyE from pDR111 and XylR from the ''B.subtilis'' genome | #PCR clone AmyE from pDR111 and XylR from the ''B.subtilis'' genome | ||
| - | |||
| - | |||
| - | |||
| - | + | ===Microscope=== | |
| + | #Prepare ''B.subtilis'' for first microscopy session on thursday - a set of dilutions to ascertain optimal amount of cells per mL | ||
| + | #Chris, James, Prudence and Clinton will attend microscope training | ||
| + | |||
| + | == DRYLAB TEAM== | ||
#Finish up tutorial 2 by this week | #Finish up tutorial 2 by this week | ||
#Start working on tutorial 3 | #Start working on tutorial 3 | ||
#Attend microscope training | #Attend microscope training | ||
#Generate data sets from bacteria motility movies | #Generate data sets from bacteria motility movies | ||
Revision as of 22:47, 7 August 2008
Contents |
WETLAB TEAM
B.subtilis
Begin culturing B.subtilis and transformation:
- Monday
- Prepare an overnight culture of DL1-blue E.coli with the pDR110 integration vector,
- Prepare an 2x overnight culture of B.subtilis,
- Prepare the reagents required for transformation,
- Tuesday
- Miniprep of the DL1-blye overnight culture,
- Make competent cells for both of the transformation protocols
- Wednesday
- 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.
- Friday
- Check successfulness of the linear DNA transformation,
Produce cell number against OD600nm calibration curve for use in characterisation Do we want to do this next week or the following week?
Cloning
- Transform XL1-blue E.coli with Biobricks containing BBa_B0015 and BBa_c0012
- Design all primers for PCR cloning
- PCR clone AmyE from pDR111 and XylR from the B.subtilis genome
Microscope
- Prepare B.subtilis for first microscopy session on thursday - a set of dilutions to ascertain optimal amount of cells per mL
- Chris, James, Prudence and Clinton will attend microscope training
DRYLAB TEAM
- Finish up tutorial 2 by this week
- Start working on tutorial 3
- Attend microscope training
- Generate data sets from bacteria motility movies
