Difference between revisions of "Template:Team:Groningen/CONTENT/EXPERIMENTS/PCR (pg10)"
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<div class="field fw4">Dreamtaq polymerase</div> | <div class="field fw4">Dreamtaq polymerase</div> | ||
<div class="field fw3">1 µL</div> | <div class="field fw3">1 µL</div> | ||
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<div class="field fw3">Time</div> | <div class="field fw3">Time</div> | ||
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<div class="record"> | <div class="record"> | ||
<div class="field fw1">1</div> | <div class="field fw1">1</div> | ||
Revision as of 22:08, 21 November 2015
12:00, 21 July 2015 - 13:00, 21 July 2015
Ordered PGA from IDT in 2 parts was PCRed to obtain the whole PGA. Used an decreasing annealing temp after each 5 cycli.
The following PCR mix was prepared.
Compound
Amount
Dreamtaq polymerase
1 µL
Dreamtaq 10x buffer
2 µL
Template DNA
1 µL
Each primer
0.3 µL
\( \mathrm{H_2O}\)
16 µL
PCR components.
The following thermocycle was used for the PCR.
#
Step
Temperature
Time
1
Initial denaturation
98 °C
5:00
2
Denaturation
98 °C
0:10
3
Annealing
75 °C
0:30
4
Extension
72 °C
2:00
5
Go back to step 2 (5x)
6
Denaturation
98 °C
0:10
7
Annealing
60 °C
0:30
8
Extension
72 °C
2:00
9
Go back to step 6 (5x)
10
Denaturation
98 °C
0:10
11
Annealing
58 °C
0:30
12
Extension
72 °C
2:00
13
Go back to step 10 (5x)
14
Denaturation
98 °C
0:10
15
Annealing
55 °C
0:30
16
Extension
72 °C
2:00
17
Go back to step 14 (5x)
18
Denaturation
98 °C
0:10
19
Annealing
50 °C
0:30
20
Extension
72 °C
2:00
21
Go back to step 18 (5x)
22
Denaturation
98 °C
0:10
23
Annealing
45 °C
0:30
24
Extension
72 °C
2:00
25
Go back to step 22 (5x)
26
Final extention
72 °C
10:00
PCR Thermocycle.
PCR product was loaded (1µL product + 4µL H2O + 1µL 6X loading buffer) on 1% agarose gel with 1:50000 SERVA DNA Stain G and gel was ran for 30min at 100V. Multiple bands visible on the gel.
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