Imperial College/21 August 2008
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m (New page: ==Dry Lab== * Generated a synthetic video of a bacterium swimming as it would be seen from the microscope, i.e with a noisy background, with realistic cell and background intensities * T...) |
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+ | {{Imperial/StartPage}}__NOTOC__ | ||
+ | {| cellpadding="10" border="0" | ||
+ | |- valign="top" | ||
+ | |{{#calendar: title=Imperial_College |year=2008 | month=07}} | ||
+ | |{{#calendar: title=Imperial_College |year=2008 | month=08}} | ||
+ | |{{#calendar: title=Imperial_College |year=2008 | month=09}} | ||
+ | | rowspan="2" bgcolor=#fff width="100%" | | ||
+ | |} | ||
+ | = 21 August 2008 = | ||
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==Dry Lab== | ==Dry Lab== | ||
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== Wet Lab== | == Wet Lab== | ||
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* Some parts of the registry ( notably GFP terminator) were double digested | * Some parts of the registry ( notably GFP terminator) were double digested | ||
+ | ===''B.subtilis''=== | ||
+ | * The ''B.subtilis'' was successfully transformed using transformation of protocol 2, [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/Prototype/Wetlab/Transformation_protocol_4#Transformation_Protocol_2| Click link here for protocol]. However, colonies were seen on the plates were no DNA was used for transformation. The most likely cayse of this is contamination whilst carrying out the electroporation. To check that the LB agar plates contained streptinomycin we picked a transformed colony and streaked it out on a freshly made LB agar plate containing streptinmycin. |
Revision as of 15:15, 25 August 2008
21 August 2008Dry Lab
Wet Lab
B.subtilis
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