Imperial College/14 August 2008
From 2008.igem.org
(Difference between revisions)
m |
|||
(2 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | {{Imperial/ | + | {{Imperial/StartPage2}}__NOTOC__ |
{| cellpadding="10" border="0" | {| cellpadding="10" border="0" | ||
|- valign="top" | |- valign="top" | ||
Line 12: | Line 12: | ||
==Wet Lab== | ==Wet Lab== | ||
- | ===Cloning=== | + | === Cloning === |
*Parts taken from the registry and transformed by electroporation into XL1-Blue ''E.coli'' along with XL1-Blue controls and grown on Kanamycin and Ampicillin plates. Parts taken: | *Parts taken from the registry and transformed by electroporation into XL1-Blue ''E.coli'' along with XL1-Blue controls and grown on Kanamycin and Ampicillin plates. Parts taken: | ||
Line 37: | Line 37: | ||
*Chris, Clinton, James and Prudence received microscope training on Widefield 1, recording two 60s videos of ''B.subtilis'' swimming for analysis | *Chris, Clinton, James and Prudence received microscope training on Widefield 1, recording two 60s videos of ''B.subtilis'' swimming for analysis | ||
- | *Determined that best results would be obtained by bringing a ''B.subtilis'' overnight culture to the microscope facility and diluting 100 fold | + | *Determined that best results would be obtained by bringing a ''B.subtilis'' overnight culture to the microscope facility and diluting 100 fold. |
+ | <br> | ||
+ | {{Imperial/EndPage|Notebook|Notebook}} |
Latest revision as of 20:36, 28 October 2008
14 August 2008Wet LabCloning
B.subtilis
Dry Lab
Microscope
|