Imperial College/20 August 2008
From 2008.igem.org
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===''B.subtilis''=== | ===''B.subtilis''=== | ||
*The transformation protocol 2, [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/Prototype/Wetlab/Transformation_protocol_4#Transformation_Protocol_2| Click link here for protocol] was carried out on competent cells that had been grown to an O.D.<sub>600</sub> of 1.8. | *The transformation protocol 2, [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/Prototype/Wetlab/Transformation_protocol_4#Transformation_Protocol_2| Click link here for protocol] was carried out on competent cells that had been grown to an O.D.<sub>600</sub> of 1.8. | ||
- | *The following concentrations of pDR110 DNA was used from the stock of | + | *The following concentrations of pDR110 DNA was used from the stock of 40ng/ul; 0, 40ng, 200ng, 400ng. One problem to note is that although the voltage and resistance can be controlled the pulse length cannot. The pulse length controls the length of time that the bacterium is exposed to the voltage. One problem is that if the pulse length drops below about 4msec, the efficiency of transformation is very low. In this set of transformations a range of 3msec to 10msec were seen. |
==Dry Lab== | ==Dry Lab== |
Revision as of 15:10, 25 August 2008
20 August 2008Wet Lab
B.subtilis
Dry Lab
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