Brown: Team Resistance/25 October 2008
From 2008.igem.org
(→Conductance/Lysis Re-test) |
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EcoRI/SpeI digest | EcoRI/SpeI digest | ||
*Used Buffer B due to potential star activity with EcoRI | *Used Buffer B due to potential star activity with EcoRI | ||
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+ | ====Conductance/Lysis Re-test==== | ||
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+ | *Same method as oct 22 but used 50 mL of same culture as control and test | ||
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+ | *Time control Test | ||
+ | OD OD | ||
+ | *0 0.064 0.063 | ||
+ | *15 0.061 0.061 | ||
+ | *30 0.072 0.065 | ||
+ | *45 0.074 0.072 | ||
+ | *60 0.077 0.074 | ||
+ | *75 0.081 0.078 | ||
+ | *90 0.085 0.084 | ||
+ | *105 0.089 0.088 | ||
+ | *120 0.093 0.086 | ||
+ | *135 0.093 0.092 | ||
+ | *150 0.088 0.087 | ||
+ | *165 0.086 0.09 | ||
+ | *180 0.092 0.09 | ||
+ | *195 0.089 0.083 | ||
+ | *210 0.091 0.089 | ||
+ | *225 0.095 0.088 | ||
+ | *240 0.089 0.089 | ||
+ | *255 0.09 0.083 | ||
+ | *270 0.087 0.086 | ||
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+ | *For some reason, the conductivity of the control solution is always greater than that of the test solution. Most likely due to calibration of the two meters |
Revision as of 11:34, 27 October 2008
25 October 2008Conductance/Lysis Re-testSame method as oct 22 but used 50 mL of same culture as control and test For some reason, the conductivity of the control solution is always greater than that of the test solution. Most likely due to calibration of the two meters At T=180min, added 600ul more arabinose solution, to make culture with 2% arabinose 2% 50mL solution = 1.04 mL At T=205, added 1mL more arabinose to actually make it 2% solution Cells did not lyse today. Perhaps wrong plasmid used. Will make culture of s different glycerol stock for test tomorrow. For purposes of current method, 50mL of culture is not needed for each test. Will test 15mL of each culture tomorrow (total 30mL)and perhaps arabinose induction will be more efficient. pVJ4 biobrickconcentration miniprep: 63.6ng/ul Ran gel of part:
EcoRI/SpeI digest
Conductance/Lysis Re-test
OD OD
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