Difference between revisions of "Template:Team:Groningen/CONTENT/PROTOCOLS/PCR"
Line 48: | Line 48: | ||
<div class="caption">PCR Mix.</div> | <div class="caption">PCR Mix.</div> | ||
</div> | </div> | ||
+ | </html> | ||
+ | }} | ||
+ | |||
+ | {{Team:Groningen/TEMPLATES/STEP | ||
+ | |title=Vortex | ||
+ | |content=<html> | ||
<div class="text">2. Gently vortex the samples and spin down.</div> | <div class="text">2. Gently vortex the samples and spin down.</div> | ||
+ | </html> | ||
+ | }} | ||
+ | |||
+ | {{Team:Groningen/TEMPLATES/STEP | ||
+ | |title=Thermal Cycle | ||
+ | |content=<html> | ||
+ | |||
<div class="text">3. Place the reactions in a thermal cycler. Perform PCR using recommended thermal cycling conditions. </div> | <div class="text">3. Place the reactions in a thermal cycler. Perform PCR using recommended thermal cycling conditions. </div> | ||
<div class="object data" id="tbl2"> | <div class="object data" id="tbl2"> |
Revision as of 13:27, 22 August 2015
PCR mix
1. Create the following mix.
Ingredient
20 μl reaction
Final Concentration
\( \mathrm{H_2O}\)
Add to 20 μl
5x Phusion HF buffer*
4 μl
1x
10 mM dNTPs
0.4 μl
200 μM each
Forward primer**
X μl
0.5 μM
Template DNA
X μl
(DMSO***, optional)
(0.6 μl)
(3%)
Phusion DNA polymerase
0.2 μl
0.02 U/ μL
Vortex
2. Gently vortex the samples and spin down.
Thermal Cycle
3. Place the reactions in a thermal cycler. Perform PCR using recommended thermal cycling conditions.
Cycle Step
Temperature
Time
Cycle
Initial denaturation
98 °C
30 s
1
Denaturation
98 °C
5-10 s
25-35
Annealing
T m - 5°C
10-30 s
25-35
Extension
72 °C
15-30 s/kb
25-35
Final extension
72°C
5-10 min
1
Hold
4 °C
Hold
1