Team:Exeter/lab book/gibs/wk7

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     <!--Project Division Links-->
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      <a href="https://2012.igem.org/Team:Exeter/lab_book/proto"; style="color:#57b947">Protocols</a>
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      &nbsp;|&nbsp;
       <a href="https://2012.igem.org/Team:Exeter/lab_book/1gp/wk1"; style="color:#57b947">Single Gene Plasmids and Enzyme Characterisation</a>
       <a href="https://2012.igem.org/Team:Exeter/lab_book/1gp/wk1"; style="color:#57b947">Single Gene Plasmids and Enzyme Characterisation</a>
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       &nbsp;|&nbsp;
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         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk1"; style="color:#1d1d1b">9th - 13th July</a>
         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk1"; style="color:#1d1d1b">9th - 13th July</a>
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         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6"; style="color:#1d1d1b">13th - 24th August</a>
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         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6"; style="color:#1d1d1b">13th - 17th August</a>
         <p>
         <p>
         -
         -
         </p>
         </p>
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         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk7"; style="color:#1d1d1b">27th - 31st August</a>
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         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk7"; style="color:#1d1d1b">20th - 24th August</a>
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        <p>
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        -
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        </p>
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        <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk8"; style="color:#1d1d1b">27th - 31st August</a>
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        <p>
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        -
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        </p>
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        <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk9"; style="color:#1d1d1b">3rd - 7th September</a>
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        <p>
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        -
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        </p>
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        <a href="https://2012.igem.org/Team:Exeter/Results#usepoly"; style="color:#e30614" target="_blank"><font size="3"><b>Results: Part 1</b></font></a>
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        <p>
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        -
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        </p>
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        <a href="https://2012.igem.org/Team:Exeter/Results/GvsB"; style="color:#e30614" target="_blank"><font size="3"><b>Results: Part 2</b></font></a>
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       <p><b><u>Operon Construction: 27th - 31st August 2012</u></b></p>
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       <p><b><u>Operon Construction: 20th - 24th August 2012</u></b></p>
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     <!------------ENTER LAB BOOK HERE: PLEASE INCLUDE DATES WITHIN THE WEEK------------>  
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     <!<p><b>**Tuesday 21.8.12**</b></p><br><p>
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A digestion and gel of constructs made previously was run by Freddie. See lab book for 3 gene inducible plasmid for details. </p><br><p>
 +
 
 +
2 step PCR of <i>wbbC</i> from genome</p><p>
 +
<a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>Two step PCR</u></a></p><p>
 +
Extra cycles at a lower annealing temperature were included due to primer overhangs not having DNA to anneal to in initial cycles</p><br><p>
 +
 
 +
PCR setup: </p><p>
 +
98°C for 30s</p><p>
 +
98°C for 10s, 55°C for 30s – X 5</p><p>
 +
98°C for 10s, 72°C for 30s – X 25</p><p>
 +
72°C for 5mins</p><p>
 +
Hold temp. 4 °C</p><br><p>
 +
 
 +
Reaction 1: <i>fadR</i> control</p><p>
 +
Reaction 2: genomic DNA</p><p>
 +
DNA (10 ng/µl) – 2 µl</p><p>
 +
Water – 34 µl</p><br><p>
 +
 
 +
5 ml PCR reaction mix run on gel</p><br><p>
 +
 
 +
 
 +
<b>**Wednesday 22.8.12**</b></p><br><p>
 +
 
 +
PCR of <i>wbbC</i> from genomic DNA</p><p>
 +
<a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>Two step PCR</u></a></p><p>
 +
DNA for attempt 1 same as before</p><br><p>
 +
 
 +
For 3/control (From <i>wbbC</i> (d) plasmid): </p><p>
 +
DNA - 0.3 µl </p><p>
 +
Water - 35.7 µl </p><br><p>
 +
 
 +
Ran gel – no joy</p><br><p>
 +
 
 +
 
 +
<b>**Thursday 23.8.12**</b></p><br><p>
 +
<a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>Two step PCR</u></a></p><p>
 +
Nanodropped genomic DNA – got ~170 and 310 ng/µl</p><p>
 +
Tried different concentrations</p><p>
 +
Control DNA 0.3 µl, water 34.7 µl</p><p>
 +
1 – 1 µl gen. DNA, 34 µl water</p><p>
 +
2 – 0.8 µl gen. DNA, 34.2 µl water</p><p>
 +
3 – 0.5 µl gen. DNA, 34.5 µl water</p><p>
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4 – 0.1 µl gen. DNA, 34.9 µl water</p><br><p>
 +
Gel ran– no luck</p><br><p>
 +
 
 +
Second go: </p><p>
 +
<a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>Two step PCR</u></a></p><p>
 +
Control – 0.3 µl DNA, water 34.7 µl</p><p>
 +
1 – 10 µl gen. DNA, 26 µl water</p><p>
 +
2 – 20 µl gen. DNA, 16 µl water</p><br><p>
 +
 
 +
<b>**Friday 24.8.12**</b></p><br><p>
 +
 
 +
PCR</p><p>
 +
Control – same</p><p>
 +
1.5 µl of DMSO added</p><p>
 +
Freddie then attempted a gradient PCR with serial dilutions of genomic DNA (see lab book for 3 gene inducible plasmid) </p>
      
      
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    <p><u>Website Designed and Built by: Ryan Edginton, James Lynch & Alex Clowsley</u> &nbsp;&nbsp;|&nbsp;&nbsp;
 +
    <a href="https://igem.org/Team.cgi?id=764" style="color:#57B947" target="_blank"><u>Contact Us</u></a>  &nbsp;&nbsp;|&nbsp;&nbsp;
 +
    <a href="https://2012.igem.org/Team:Exeter/site_map" style="color:#57B947"><u>Site Map</u></a></p>
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Latest revision as of 00:10, 27 September 2012

ExiGEM2012 Lab Book Gibs wk7

Operon Construction: 20th - 24th August 2012

**Tuesday 21.8.12**


A digestion and gel of constructs made previously was run by Freddie. See lab book for 3 gene inducible plasmid for details.


2 step PCR of wbbC from genome

Two step PCR

Extra cycles at a lower annealing temperature were included due to primer overhangs not having DNA to anneal to in initial cycles


PCR setup:

98°C for 30s

98°C for 10s, 55°C for 30s – X 5

98°C for 10s, 72°C for 30s – X 25

72°C for 5mins

Hold temp. 4 °C


Reaction 1: fadR control

Reaction 2: genomic DNA

DNA (10 ng/µl) – 2 µl

Water – 34 µl


5 ml PCR reaction mix run on gel


**Wednesday 22.8.12**


PCR of wbbC from genomic DNA

Two step PCR

DNA for attempt 1 same as before


For 3/control (From wbbC (d) plasmid):

DNA - 0.3 µl

Water - 35.7 µl


Ran gel – no joy


**Thursday 23.8.12**


Two step PCR

Nanodropped genomic DNA – got ~170 and 310 ng/µl

Tried different concentrations

Control DNA 0.3 µl, water 34.7 µl

1 – 1 µl gen. DNA, 34 µl water

2 – 0.8 µl gen. DNA, 34.2 µl water

3 – 0.5 µl gen. DNA, 34.5 µl water

4 – 0.1 µl gen. DNA, 34.9 µl water


Gel ran– no luck


Second go:

Two step PCR

Control – 0.3 µl DNA, water 34.7 µl

1 – 10 µl gen. DNA, 26 µl water

2 – 20 µl gen. DNA, 16 µl water


**Friday 24.8.12**


PCR

Control – same

1.5 µl of DMSO added

Freddie then attempted a gradient PCR with serial dilutions of genomic DNA (see lab book for 3 gene inducible plasmid)

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