Team:Exeter/lab book/gibs/wk7

From 2012.igem.org

(Difference between revisions)
Line 85: Line 85:
         -
         -
         </p>
         </p>
-
         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk10"; style="color:#1d1d1b">10th - 14th September</a>
+
         <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>
         <p>
         <p>
         -
         -
         </p>
         </p>
-
         <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk11"; style="color:#1d1d1b">17th - 21st September</a>
+
         <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>
-
        <p>
+
-
        -
+
-
        </p>
+
-
        <a href="https://2012.igem.org/Team:Exeter/Results#usepoly"; style="color:#e30614"><font size="3"><b>Results: Part 1</b></font></a>
+
-
        <p>
+
-
        -
+
-
        </p>
+
-
        <a href="https://2012.igem.org/Team:Exeter/Results/GvsB"; style="color:#e30614"><font size="3"><b>Results: Part 2</b></font></a>
+
       </font>
       </font>
     </div>
     </div>

Revision as of 21:34, 26 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)