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<math>_{2}</math>
+
*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}