Team:Macquarie Australia/Protocols/PCR
From 2013.igem.org
(Difference between revisions)
(Created page with "{{Team:Macquarie_Australia/Style2}} {{Team:Macquarie_Australia/Header}} <center><h1>Polymerase Chain Reaction</h1></center> <html> <b>PCR mixture</b> <br> 4.0ul 5x phusio...") |
|||
Line 18: | Line 18: | ||
1ul reverse primer | 1ul reverse primer | ||
1ul template | 1ul template | ||
- | + | <br><br> | |
<b>PCR settings</b> | <b>PCR settings</b> | ||
<br> | <br> |
Revision as of 04:46, 29 August 2013
Polymerase Chain Reaction
PCR mixture
4.0ul 5x phusion buffer
0.4ul dNTPs
0.6ul DMSO
0.2ul Polymerase
11.8ul water
Total 17ul
1ul forward primer
1ul reverse primer
1ul template
PCR settings
Initial denaturation 98oC for 30 secs
Followed by 30 repears of:
Denaturation 98 oC 10 secs
Annealing 60 oC 10 secs
Extension 72 oC 2 mins
Final extension 72 oC 10 mins