From 2010.igem.org
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| == Group: Flagella == | | == Group: Flagella == |
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| + | === Annealing of the two mutated strands of FlhDC === |
| <br> | | <br> |
| + | ''Experiment done by:'' Sheila <br><br> |
| + | ''Date:'' July 19th <br><br> |
| + | ''Protocol:'' [https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP1.1]<br><br> |
| + | ''Method:'' PCR of the two mutated strands of the FlhDC operon<br><br> |
| + | ''Notes:'' To samples were run at two different temperatures: 56,1˚C and 64,5˚C respectively. <br>Polymerase used: Pfu<br> Primers used: None, as the two strands are supposed to anneal to each other<br><br> |
| + | ''Results:''<br><br> |
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| == Group: Photosensor == | | == Group: Photosensor == |
| <br> | | <br> |
Revision as of 16:59, 19 July 2010
Lab notes (7/19 - 7/25)
Group: Flagella
Annealing of the two mutated strands of FlhDC
Experiment done by: Sheila
Date: July 19th
Protocol: CP1.1
Method: PCR of the two mutated strands of the FlhDC operon
Notes: To samples were run at two different temperatures: 56,1˚C and 64,5˚C respectively.
Polymerase used: Pfu
Primers used: None, as the two strands are supposed to anneal to each other
Results:
Group: Photosensor
Group: Retinal
Transformation of K081005 in pSB1A2 (constitutive promoter and RBS combined),R0011 in pSB1A2, pSB3C5 w. J04450 and pSB3T5 w. J04450 in Top 10 E.Coli
Start date: 19/07 End date: 20/07
Methods: ON culture, making competent cells, transformation
Protocol:CC1.1 TR1.1
Experiment done by: Maria
Notes:ON colony was made of 110 ml lb medium inoculated with a top10 coloni.
Time
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Optical density
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8:12
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2.9
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8:17
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0.02
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9:17
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0.035
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10:17
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0.204
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10:40
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0.380
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10:50
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0.49
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pSB1A2 w. R0011 and pSB1A2 w. K081005 was plated with 150uL on plates containing LA, LA + Amp, LA + Tetracycline, LA + Chloramphenicol and LA + Kanamycine.Upconcentration of these samples was not made. pSB3T5 w. J04450 and pSB3C5 w. J04450 was plated according to protocol
Results:
Analysis:
--
Tipi 16:33, 19 July 2010 (UTC)
Include column content here.