User:University of Washington/5 September 2008

From 2008.igem.org

(Difference between revisions)
(LuxR from AraC and TetR(Faifan))
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- diluted 1 ml culture into 5 ml Tsy+Kan, OD@600nm = 0.165
- diluted 1 ml culture into 5 ml Tsy+Kan, OD@600nm = 0.165
-
- set up 96 well plate reader experiment. The total volume in each well was 200 ul.
+
- set up 96 well plate reader experiment:
 +
*5x5, 160 ul culture
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{|
+
{| style="text-align:center" border=1
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!colspan=2 rowspan=2| !!colspan=5|Arabinose(%), 10%Arabinose added (ul)
|-
|-
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!!!rowspan=5|Arabinose(%), 10%Arabinose added (ul)
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!0%, 0 ul!!0.05%, 1ul!!0.1%, 2ul!!0.50%, 10ul!!1.00%, 20ul
|-
|-
-
!!!0, 0!!0.05, 1!!0.1, 2!!0.50, 10!!1.00, 20
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!rowspan=5 valign=center|aTc(ng/ml), 10ug/ml-aTc added(ul)!!0, 0ul||||||||||
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|-
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!50, 1ul||||||||||
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|-
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!100, 2ul||||||||||
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|-
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!500, 10ul||||||||||
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|-
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!1000, 20 ul||||||||||
|}
|}
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*added dH2O to final the volume to 200 ul
 +
*added 40 ul of mineral oil to each well to protect evaporation
 +
*set the machine to run 24 hrs, read every 10 mins
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Back to [[Team:University_of_Washington/Notebook#Notebook]]
Back to [[Team:University_of_Washington/Notebook#Notebook]]

Revision as of 00:01, 6 September 2008

LuxR from AraC and TetR(Faifan)

- measured Absorbance of the overnight culture at 660 nm = 1.5

- diluted 60 ul culture into 5.40 ml Tsy+KAN. Absorbance at 660 nm = 0.035

- incubated 37 degree Celsius for 2.5 hrs, Absorbance at 600 nm = 0.7

- diluted 1 ml culture into 5 ml Tsy+Kan, OD@600nm = 0.165

- set up 96 well plate reader experiment:

  • 5x5, 160 ul culture
Arabinose(%), 10%Arabinose added (ul)
0%, 0 ul0.05%, 1ul0.1%, 2ul0.50%, 10ul1.00%, 20ul
aTc(ng/ml), 10ug/ml-aTc added(ul)0, 0ul
50, 1ul
100, 2ul
500, 10ul
1000, 20 ul
  • added dH2O to final the volume to 200 ul
  • added 40 ul of mineral oil to each well to protect evaporation
  • set the machine to run 24 hrs, read every 10 mins



Back to Team:University_of_Washington/Notebook#Notebook