Team:Chiba/Notebook/Calendar/24 September 2009

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(23_September_2009 <|>25_September_2009)


Contents

Examine limit of AHL generation(1)-3

Yesterday's operation is here.


  • Today's operation

14:00

We made plates from each of mixture and 10 mL of LB-Amp, Cm solution medium.


  • Element of mixtures
Sample Namber 1 2 3 4 5 6 7 8
supernatant solution 5 mL --- --- --- --- --- --- 20 μL
1 --- 5 mL --- --- --- --- --- ---
2 --- --- 5 mL --- --- --- --- ---
3 --- --- --- 5 mL --- --- --- ---
4 --- --- --- --- 5 mL --- --- ---
5 --- --- --- --- --- 5 mL --- ---
6 --- --- --- --- --- --- 5 mL ---
LB-Amp,Cm(liquid) 10 mL 10 mL 10 mL 10 mL 10 mL 10 mL 10 mL 9.98 mL
Total 10 mL 10 mL 10 mL 10 mL 10 mL 10 mL 10 mL 10 mL

Transformation(2)-2

Yesterday's operation is here.


  • Today's operation

11:15-

We picked colony(plux-GFP only) and cultured it.


15:50-

Main culture


20:30-

Mini prep.

And resultant DNA was saved in freezer.


Transformation(3)-1

  • Plasmids

ptet-GFP pSB1A2 [http://partsregistry.org/Part:BBa_I13522 BBa_I13522](Amp)

ptet-RFP pSB1A3 [http://partsregistry.org/Part:BBa_I13521 BBa_I13521](Amp)

ptet-CFP pSB1A2 [http://partsregistry.org/Part:BBa_I13600 BBa_I13600](Amp)

mRFP without Nco1 site(Cm)


  • Competent Cells

JW1262


21:50-

We cultured each plates.


Digestion Test

  • Samples

1 : ECFP([http://partsregistry.org/Part:BBa_I6057 BBa_I6057])

2 : mCherry([http://partsregistry.org/Part:BBa_E2060 BBa_E2060])

3 : V-YFP([http://partsregistry.org/Part:BBa_K084003 BBa_K084003])

4 : mOrange([http://partsregistry.org/Part:BBa_E2050 BBa_E2050])

5 : LacZ α([http://partsregistry.org/Part:BBa_T9003 BBa_T9003])

6 : mRFP without Nco1 site

  • Doble Digestion
Sample 3 μL
EcoR1 0.20 μL
Pst1 0.20 μL
Buffer 1 μL
BSA 1 μL
dw 4.6 μL
Total 10 μL


  • Doble Digestion's Master Mix
Sample 3 μL
EcoR1 1.4 μL
Pst1 1.4 μL
Buffer 7 μL
BSA 7 μL
dw 32.2 μL
Total 49 μL


  • Single Digestion
Sample 3 μL
EcoR1 0.20 μL
Buffer 1 μL
dw 6.8 μL
Total 10 μL


  • Single Digestion's Master Mix
EcoR1 1.4 μL
Buffer 7 μL
dw 40.6 μL
Total 49 μL



12:50

Warm up at 37 degrees Celsius


13:30

Gel electrophoretic analysis

To judge character of LuxR mutants(3)-1

We poured 1 mL of LB-Amp, Cm liquid medium in 96 deep well and added glycerol stocks.


22:10-

We cultured and shook it at 37 degrees Celsius.