Team:Chiba/Calendar-Home/19 September 2008

From 2008.igem.org

(Difference between revisions)
Line 13: Line 13:
</tr>
</tr>
<tr>
<tr>
-
<td>Sample DNA(μL)</td>
+
<td>Sample DNA(&mu;L)</td>
<td>30</td><td>30</td><td>90</td><td>?</td>
<td>30</td><td>30</td><td>90</td><td>?</td>
</tr>
</tr>
<tr>
<tr>
-
<td>Loading Dye(μL)</td>
+
<td>Loading Dye(&mu;L)</td>
<td>6</td><td>6</td><td>18</td><td>?</td>
<td>6</td><td>6</td><td>18</td><td>?</td>
</tr>
</tr>
<tr>
<tr>
-
<td>TOTAL(μL)</td>
+
<td>TOTAL(&mu;L)</td>
<td>36</td><td>36</td><td>108</td><td>24</td>
<td>36</td><td>36</td><td>108</td><td>24</td>
</tr>
</tr>
Line 27: Line 27:
--->'''[[Team:Chiba/protocol/ligation/gelex|Gel Extract]]'''<br>
--->'''[[Team:Chiba/protocol/ligation/gelex|Gel Extract]]'''<br>
-
(各サンプル well3つずつ)<br>
+
(3 wells for 1 sample)<br>
-
*note:ADB buffer添加後,37℃,6h
+
*note:ADB buffer添加後,left at 37&deg;C,for 6 hours
:--->'''[[Team:Chiba/protocol/DNA Purification/zymocleam|Zymo Clean]]'''
:--->'''[[Team:Chiba/protocol/DNA Purification/zymocleam|Zymo Clean]]'''
*elution
*elution
-
**J0450-->27μL
+
**J0450-->27&mu;L
-
**C0161-->11μL
+
**C0161-->11&mu;L
--->'''[[Team:Chiba/protocol/gelcheck|Gel Check]]'''
--->'''[[Team:Chiba/protocol/gelcheck|Gel Check]]'''
Line 43: Line 43:
</tr>
</tr>
<tr>
<tr>
-
<td>C0161(μL)</td>
+
<td>C0161(&mu;L)</td>
<td>3</td><td>3</td><td>-</td>
<td>3</td><td>3</td><td>-</td>
</tr>
</tr>
<tr>
<tr>
-
<td>J04500(μL)</td>
+
<td>J04500(&mu;L)</td>
<td>4.5</td><td>-</td><td>4.5</td>
<td>4.5</td><td>-</td><td>4.5</td>
</tr>
</tr>
<tr>
<tr>
-
<td>ligase(μL)</td>
+
<td>ligase(&mu;L)</td>
<td>1</td><td>1</td><td>1</td>
<td>1</td><td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>Buffer(invitrogen)(μL)</td>
+
<td>Buffer(invitrogen)(&mu;L)</td>
<td>3</td><td>2</td><td>2</td>
<td>3</td><td>2</td><td>2</td>
</tr>
</tr>
<tr>
<tr>
-
<td>NFW?(μL)</td>
+
<td>NFW(&mu;L)</td>
<td>3.5</td><td>4</td><td>2.5</td>
<td>3.5</td><td>4</td><td>2.5</td>
</tr>
</tr>
<tr>
<tr>
-
<td>TOTAL(μL)</td>
+
<td>TOTAL(&mu;L)</td>
<td>15</td><td>10</td><td>10</td>
<td>15</td><td>10</td><td>10</td>
</tr>
</tr>
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*note
*note
**competent cell:XL10GOLD
**competent cell:XL10GOLD
-
**DNA:1μL,SOC:120μL
+
**DNA:1&mu;L,SOC:120&mu;L
--->(20/9)'''[[Team:Chiba/protocol/DNA Purification/sigma|Mini prep]]
--->(20/9)'''[[Team:Chiba/protocol/DNA Purification/sigma|Mini prep]]
Line 81: Line 81:
#temparature
#temparature
-
30℃ and Room Temparature
+
30&deg;C and Room Temparature
===Team:Output===
===Team:Output===
<br>colony PCR
<br>colony PCR
-
<br>ptet+LuxR(x16)
+
<br>ptet+LuxR(&times;16)
-
<br>ptet+LasR(x7)
+
<br>ptet+LasR(&times;7)
-
<br>ptet+RhlR(x5)
+
<br>ptet+RhlR(&times;5)
-
<br>ptet+cinR(x5)
+
<br>ptet+cinR(&times;5)

Revision as of 19:53, 29 October 2008

>Home | Notebook

18 September 2008 <|> 20 September 2008

Laboratory work

Team:Communication

-->(?/9) Gel Check

Sample Name J04500R0010C0161Cin
Sample DNA(μL) 303090?
Loading Dye(μL) 6618?
TOTAL(μL) 363610824

--->Gel Extract
(3 wells for 1 sample)

  • note:ADB buffer添加後,left at 37°C,for 6 hours
--->Zymo Clean
  • elution
    • J0450-->27μL
    • C0161-->11μL

--->Gel Check

--->Ligation
Sample Name insert+vectorinsertvector
C0161(μL) 33-
J04500(μL) 4.5-4.5
ligase(μL) 111
Buffer(invitrogen)(μL) 322
NFW(μL) 3.542.5
TOTAL(μL) 151010
--->Transformed above ligation onto a LB-amp plate.
  • note
    • competent cell:XL10GOLD
    • DNA:1μL,SOC:120μL

--->(20/9)Mini prep


  1. strain
    Senders:XL10GOLD
    Receiver:JW1908
  2. temparature

30°C and Room Temparature

Team:Output


colony PCR
ptet+LuxR(×16)
ptet+LasR(×7)
ptet+RhlR(×5)
ptet+cinR(×5)