"
Team:LMU-Munich/Notebook/Protocols/16 PCR with DreamTaq
From 2010.igem.org
(New page: {{:Team:LMU-Munich/Templates/Page Header}} <b>PCR with DreamTaq</b> In a sterile, nuclease free PCR-tube mix following components: {| |- |Component |Volume |Final concentration |- |Dre...) |
|||
| Line 36: | Line 36: | ||
|- | |- | ||
| - | |Dream Taq Polymerase | + | |Dream Taq Polymerase |
|0,5µl | |0,5µl | ||
|~1,25u/50µl | |~1,25u/50µl | ||
Revision as of 07:57, 1 September 2010
In a sterile, nuclease free PCR-tube mix following components:
PCR with DreamTaq
Component
Volume
Final concentration
DreamTaq Polymerase 10x Buffer (with MgSO4)
5 µl
1x
dNTP 10mM each
1µl
200µM each
upstream primer
5-50pmol (from 100pmol/µl e.g. 2,5µl)
0,1- 1 µM
downstream primer
5-50pmol (from 100pmol/µl e.g. 2,5µl)
0,1- 1 µM
DNA Template
variable (dependent on DNA conc.)
<0,5µg/50µl (e.g. 0,3)
Dream Taq Polymerase
0,5µl
~1,25u/50µl
DMSO
1,25µl
nuclease free water to final volume of
50 µl
Recommended thermal cycling conditions for DreamTaq Polymerase:
Step
Temperature
Time
Number of Cycles
Initial Denaturation
95°C
3min
1
Denaturation
95°C
0,5min
Annealing
42-65°C (dependent on primer and template)
30sec
25-35
Extension
72°C
1min
Final Extension
72°C
5 min
10
Soak (end)
4°C (on our thermalcyclers 12°C)
Indefinite
1
