Difference between revisions of "Template:Team:Groningen/CONTENT/PROTOCOLS/PCR"
Line 7: | Line 7: | ||
<div class="header"> | <div class="header"> | ||
<div class="field fw5">Ingredient</div> | <div class="field fw5">Ingredient</div> | ||
− | <div class="field fw3">20 | + | <div class="field fw3">20 μL reaction</div> |
<div class="field fw3">Final Concentration</div> | <div class="field fw3">Final Concentration</div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">\( \mathrm{H_2O}\)</div> | <div class="field fw5">\( \mathrm{H_2O}\)</div> | ||
− | <div class="field fw3">Add to 20 | + | <div class="field fw3">Add to 20 μL</div> |
<div class="field fw3"></div> | <div class="field fw3"></div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">5x Phusion HF buffer*</div> | <div class="field fw5">5x Phusion HF buffer*</div> | ||
− | <div class="field fw3">4 | + | <div class="field fw3">4 μL</div> |
<div class="field fw3">1x</div> | <div class="field fw3">1x</div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">10 mM dNTPs</div> | <div class="field fw5">10 mM dNTPs</div> | ||
− | <div class="field fw3">0.4 | + | <div class="field fw3">0.4 μL</div> |
<div class="field fw3">200 μM each</div> | <div class="field fw3">200 μM each</div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">Forward primer**</div> | <div class="field fw5">Forward primer**</div> | ||
− | <div class="field fw3">X | + | <div class="field fw3">X μL</div> |
<div class="field fw3">0.5 μM</div> | <div class="field fw3">0.5 μM</div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">Template DNA</div> | <div class="field fw5">Template DNA</div> | ||
− | <div class="field fw3">X | + | <div class="field fw3">X μL</div> |
<div class="field fw3"></div> | <div class="field fw3"></div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">(DMSO***, optional)</div> | <div class="field fw5">(DMSO***, optional)</div> | ||
− | <div class="field fw3">(0.6 | + | <div class="field fw3">(0.6 μL)</div> |
<div class="field fw3">(3%)</div> | <div class="field fw3">(3%)</div> | ||
</div> | </div> | ||
<div class="record"> | <div class="record"> | ||
<div class="field fw5">Phusion DNA polymerase</div> | <div class="field fw5">Phusion DNA polymerase</div> | ||
− | <div class="field fw3">0.2 | + | <div class="field fw3">0.2 μL</div> |
<div class="field fw3">0.02 U/ μL</div> | <div class="field fw3">0.02 U/ μL</div> | ||
</div> | </div> |
Latest revision as of 21:50, 21 November 2015
PCR mix
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
Gently vortex the samples and spin down.
Thermal Cycle
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