Team:Chiba/Calendar-Home/20 August 2008

From 2008.igem.org

(Difference between revisions)
(Team:Communication)
(Team:Input)
Line 17: Line 17:
</tr>
</tr>
<tr>
<tr>
-
<td>DNA tamplate</td>
+
<td>DNA tamplate(&mu;L)</td>
-
<td>1</td><td>1</td><td>1</td><td>1</td>><td>1</td>
+
<td>1</td><td>1</td><td>1</td><td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>FW primer</td>
+
<td>FW primer(&mu;L)</td>
<td>5</td><td>5</td><td>5</td><td>5</td><td>5</td>
<td>5</td><td>5</td><td>5</td><td>5</td><td>5</td>
</tr>
</tr>
<tr>
<tr>
-
<td>VR primer</td>
+
<td>VR primer(&mu;L)</td>
<td>5</td><td>5</td><td>5</td><td>5</td><td>5</td>
<td>5</td><td>5</td><td>5</td><td>5</td><td>5</td>
</tr>
</tr>
<tr>
<tr>
-
<td>dNTPmix</td>
+
<td>dNTPmix(&mu;L)</td>
<td>10</td><td>10</td><td>10</td><td>10</td><td>10</td>
<td>10</td><td>10</td><td>10</td><td>10</td><td>10</td>
</tr>
</tr>
<tr>
<tr>
-
<td>thermo pol buffer</td>
+
<td>thermo pol buffer(&mu;L)</td>
<td>10</td><td>10</td><td>10</td><td>10</td><td>10</td>
<td>10</td><td>10</td><td>10</td><td>10</td><td>10</td>
</tr>
</tr>
<tr>
<tr>
-
<td>DNA pol(VENT)</td>
+
<td>DNA pol(VENT)(&mu;L)</td>
<td>1</td><td>1</td><td>1</td><td>1</td><td>1</td>
<td>1</td><td>1</td><td>1</td><td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>dH<sub>2</sub>O</td>
+
<td>dH<sub>2</sub>O(&mu;L)</td>
<td>68</td><td>68</td><td>68</td><td>68</td><td>68</td>
<td>68</td><td>68</td><td>68</td><td>68</td><td>68</td>
</tr>
</tr>
<tr>
<tr>
-
<td>TOTAL</td>
+
<td>TOTAL(&mu;L)</td>
-
<td>100μL</td><td>100μL</td><td>100μL</td><td>100μL</td><td>100μL</td>
+
<td>100</td><td>100</td><td>100</td><td>100</td><td>100</td>
</tr>
</tr>
</table>
</table>
Line 63: Line 63:
</tr>
</tr>
<tr>
<tr>
-
<td>loading dye</td>
+
<td>loading dye(&mu;L)</td>
<td>1</td><td>1</td><td>1</td><td>1</td><td>1</td>
<td>1</td><td>1</td><td>1</td><td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>dH<sub>2</sub>O</td>
+
<td>dH<sub>2</sub>O(&mu;L)</td>
<td>4</td><td>4</td><td>4</td><td>4</td><td>4</td>
<td>4</td><td>4</td><td>4</td><td>4</td><td>4</td>
</tr>
</tr>
<tr>
<tr>
-
<td>Total</td>
+
<td>Total(&mu;L)</td>
-
<td>6μL</td><td>6μL</td><td>6μL</td><td>6μL</td><td>6μL</td>
+
<td>6</td><td>6</td><td>6</td><td>6</td><td>6</td>
</tr>
</tr>

Revision as of 05:57, 30 October 2008

>Home | Notebook

19 August 2008 <|> 21 August 2008

Contents

Laboratory work

Team:Input

PCR

Sample No. 12345
DNA tamplate(μL) 11111
FW primer(μL) 55555
VR primer(μL) 55555
dNTPmix(μL) 1010101010
thermo pol buffer(μL) 1010101010
DNA pol(VENT)(μL) 11111
dH2O(μL) 6868686868
TOTAL(μL) 100100100100100

-->Gel Check


>
Sample No. 12345
Sample DNA 11111
loading dye(μL) 11111
dH2O(μL) 44444
Total(μL) 66666

-->1,2,3,4,5:none

Transformation

Team:Communication

(18/8)--->Mini prep


--->Gel Check
Chiba-0820-3.JPG
Sample DNA 3
Loading Dye 2
dH2O 7
TOTAL 12μL
From left;


Chiba-0820-4.JPG
Sample DNA 10
Loading Dye 4
dH2O 10
TOTAL 24μL
From left;



Chiba-0820.JPG
Sample DNA 3
Loading Dye 2
dH2O 7
TOTAL 12μL
From left;


--->Digestion test

Sample No 12345678
BBa_C0170(2006) 3---3---
BBa_C0170(2007) -3---3--
BBa_C0178(2006) --3---3-
BBa_C0178(2007) ---3---3
EcoRI 0.10.10.10.10.10.10.10.1
PstI ----0.10.10.10.1
Buffer EcoRI 11111111
BSA 11111111
dH2O 4.94.94.94.94.84.84.84.8
TOTAL 10μL10μL10μL10μL10μL10μL10μL10μL


--->Gel Check
Chiba-0820-2.JPG
Sample DNA 3
Loading Dye 2
dH2O 7
TOTAL 12μL
From left;
(Single Digestion 1~4)
(Double Digestion 1~4)

Team:Output

Transformation