USTC/Notebook/PCR&Colony PCR

From 2008.igem.org

(Difference between revisions)
Line 11: Line 11:
2. add the following components:
2. add the following components:
-
  - 2µL  PCR buffer (rock gently after thawing, quick spin before use)
+
- 2µL  PCR buffer (rock gently after thawing, quick spin before use)
-
  - 1.2uL  Mgcl2
+
- 1.2uL  Mgcl2
-
  - 0.4uL  dNTPs
+
- 0.4uL  dNTPs
-
  - 200nM final concentration of each primer  
+
- 200nM final concentration of each primer  
-
  - 0.2uL Taq enzyme
+
- 0.2uL Taq enzyme
-
  - template DNA
+
- template DNA
(note: the total volume of PCR is 20µL)
(note: the total volume of PCR is 20µL)
Line 26: Line 26:
== colony PCR ==
== colony PCR ==
-
0.2 uL primer #1 (to 25uM)  
+
- 0.2 uL primer #1 (to 25uM)  
-
0.2 uL primer #2
+
- 0.2 uL primer #2
-
0.4 uL dNTPs  
+
- 0.4 uL dNTPs  
-
2 uL Buffer  
+
- 2 uL Buffer  
-
5 uL colony culture  
+
- 5 uL colony culture  
-
0.2 uL Taq  
+
- 0.2 uL Taq  
-
10.4 uL H20  
+
- 10.4 uL H20  
perform PCR with an initial heating step at 94C for 5 minutes followed by 25-35 cycles of 30sec at 94C, 30sec at 55C and 1Kb/min at 72C,and 72C for 10min
perform PCR with an initial heating step at 94C for 5 minutes followed by 25-35 cycles of 30sec at 94C, 30sec at 55C and 1Kb/min at 72C,and 72C for 10min

Revision as of 13:44, 27 October 2008

< Back to Notebook

PCR

Briefly, a typical reaction is set up as follows:


1. set up pre-labeled reaction tubes on ice

2. add the following components: - 2µL PCR buffer (rock gently after thawing, quick spin before use) - 1.2uL Mgcl2 - 0.4uL dNTPs - 200nM final concentration of each primer - 0.2uL Taq enzyme - template DNA (note: the total volume of PCR is 20µL)

3. make sure reaction tubes are properly capped before placing in thermocycler

4. perform PCR with an initial heating step at 94C for 5 minutes followed by 25-35 cycles of 30sec at 94C, 30sec at 55C and 1Kb/min at 72C


colony PCR

- 0.2 uL primer #1 (to 25uM) - 0.2 uL primer #2 - 0.4 uL dNTPs - 2 uL Buffer - 5 uL colony culture - 0.2 uL Taq - 10.4 uL H20

perform PCR with an initial heating step at 94C for 5 minutes followed by 25-35 cycles of 30sec at 94C, 30sec at 55C and 1Kb/min at 72C,and 72C for 10min