Melbourne/Lab BL Notebook/PCR1
From 2007.igem.org
(Difference between revisions)
Line 2: | Line 2: | ||
=PCR mix= | =PCR mix= | ||
- | 5ul 10x buffer | + | *5ul 10x buffer |
- | 5ul Enhancer | + | *5ul Enhancer |
- | 0.6ul dNTPs (25mM stock) | + | *0.6ul dNTPs (25mM stock) |
- | 2.5ul MgSO4 (Supplied in PCR kit) | + | *2.5ul MgSO4 (Supplied in PCR kit) |
- | 1.5ul Primer I (10uM) | + | *1.5ul Primer I (10uM) |
- | 1.5ul Primer II (10uM) | + | *1.5ul Primer II (10uM) |
- | 1ul Template ([[Melbourne/pJS010|pJS010]]) | + | *1ul Template ([[Melbourne/pJS010|pJS010]]) |
- | 0.4ul Pfx Platinum (Invitrogen) | + | *0.4ul Pfx Platinum (Invitrogen) |
- | 32.5ul ddH< | + | *32.5ul ddH<sub>_{2}</sub> |
Revision as of 14:42, 10 October 2007
Protocol for PCR reactions A-G (and -ve control) amplifying the photoreceptor and transmembrane domains of NpSopII-NpHtrII.
PCR mix
- 5ul 10x buffer
- 5ul Enhancer
- 0.6ul dNTPs (25mM stock)
- 2.5ul MgSO4 (Supplied in PCR kit)
- 1.5ul Primer I (10uM)
- 1.5ul Primer II (10uM)
- 1ul Template (pJS010)
- 0.4ul Pfx Platinum (Invitrogen)
- 32.5ul ddH_{2}