Team:Chiba/Notebook/Calendar/24 September 2009

From 2009.igem.org

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== Examine limit of AHL generation ==
+
== Examine limit of AHL generation(1)-3 ==
Yesterday's operation is [https://2009.igem.org/wiki/index.php?title=Team:Chiba/Notebook/Calendar/23_September_2009 here].  
Yesterday's operation is [https://2009.igem.org/wiki/index.php?title=Team:Chiba/Notebook/Calendar/23_September_2009 here].  
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</tr>
</tr>
<tr>
<tr>
-
<td>LB-Amp,Cm</td>
+
<td>LB-Amp,Cm(liquid)</td>
<td>10 mL</td>
<td>10 mL</td>
<td>10 mL</td>
<td>10 mL</td>
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<td>10 mL</td>
<td>10 mL</td>
<td>10 mL</td>
<td>10 mL</td>
-
<td>9.8 mL</td>
+
<td>9.98 mL</td>
</tr>
</tr>
<tr>
<tr>
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</tr>
</tr>
</table>
</table>
-
 
-
 
== Transformation(2)-2 ==
== Transformation(2)-2 ==
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-
 
+
*Single Digestion
-
*Single Digestion's Master Mix
+
<table width="100" border="1" cellpadding="0"  cellspacing="0" bordercolor="#000000"><tr>
<table width="100" border="1" cellpadding="0"  cellspacing="0" bordercolor="#000000"><tr>
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<td width="50">EcoR1</td>
+
<td width="50">Sample</td>
-
<td width="50">1.4 &mu;L</td>
+
<td width="50">3 &mu;L</td>
 +
</tr>
 +
<tr>
 +
<td>EcoR1</td>
 +
<td>0.20 &mu;L</td>
</tr>
</tr>
<tr>
<tr>
<td>Buffer</td>
<td>Buffer</td>
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<td>7 &mu;L</td>
+
<td>1 &mu;L</td>
</tr>
</tr>
<tr>
<tr>
<td>dw</td>
<td>dw</td>
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<td>40.6 &mu;L</td>
+
<td>6.8 &mu;L</td>
</tr>
</tr>
<tr>
<tr>
<td>Total</td>
<td>Total</td>
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<td>49 &mu;L</td>
+
<td>10 &mu;L</td>
</tr>
</tr>
</table>
</table>
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*Doble Digestion
+
*Single Digestion's Master Mix
<table width="100" border="1" cellpadding="0"  cellspacing="0" bordercolor="#000000"><tr>
<table width="100" border="1" cellpadding="0"  cellspacing="0" bordercolor="#000000"><tr>
-
<td width="50">Sample</td>
+
<td width="50">EcoR1</td>
-
<td width="50">3 &mu;L</td>
+
<td width="50">1.4 &mu;L</td>
-
</tr>
+
-
<tr>
+
-
<td>EcoR1</td>
+
-
<td>0.20 &mu;L</td>
+
-
</tr>
+
-
<tr>
+
-
<td>Pst1</td>
+
-
<td>0.20 &mu;L</td>
+
</tr>
</tr>
<tr>
<tr>
<td>Buffer</td>
<td>Buffer</td>
-
<td>1 &mu;L</td>
+
<td>7 &mu;L</td>
-
</tr>
+
-
<tr>
+
-
<td>BSA</td>
+
-
<td>1 &mu;L</td>
+
</tr>
</tr>
<tr>
<tr>
<td>dw</td>
<td>dw</td>
-
<td>4.6 &mu;L</td>
+
<td>40.6 &mu;L</td>
</tr>
</tr>
<tr>
<tr>
<td>Total</td>
<td>Total</td>
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<td>10 &mu;L</td>
+
<td>49 &mu;L</td>
</tr>
</tr>
</table>
</table>
 +
 +
 +
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Gel electrophoretic analysis
Gel electrophoretic analysis
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== LuxR Mutants(3)-1 ==
+
== 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-
22:10-
 +
 +
We cultured and shook it at 37 degrees Celsius.

Latest revision as of 08:03, 3 October 2009

>Go to the Notebook page

(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.

Retrieved from "http://2009.igem.org/Team:Chiba/Notebook/Calendar/24_September_2009"