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Team:EPF-Lausanne/Protocols/TetR
From 2011.igem.org
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== Materials == | == Materials == | ||
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*0.5 µl High Fidelity Polymerase | *0.5 µl High Fidelity Polymerase | ||
*1 µl DNA template | *1 µl DNA template | ||
| + | *0.5 µl Polymerase | ||
*36.5 µl H2O | *36.5 µl H2O | ||
Revision as of 12:09, 7 July 2011
Linear template- TetR
Two step extension PCR
Gene PCR
Materials
- 10µl 5x iProof HF buffer
- 0.5 µl of each primer
- 1 µl dNTP mix of 10mM
- 0.5 µl High Fidelity Polymerase
- 1 µl DNA template
- 0.5 µl Polymerase
- 36.5 µl H2O
Protocol
- Put mix in PCR thermal cycler
- Program the PCR thermal cycler: 1. 98°C for 30s 2. 98°C for 7.5 seconds 3. 58°C for 20 sec (this depends on the primers, therefore look up the annealing temperature of the primers used) 4. 72°C for 15 sec; you have to calculate the time required. This polymerase has an effciency of 15-30s/kb. (calculate for the longest fragment) 6. 72°C for 5 min 7. 4°C "forever"
- Save the file in the MAIN folder→ OK→ SAVE→RUN→Select the block you use→ RUN→ Change sample volume to 50µl, LidT should be 105°C and the box just below ("hotlid") should ALWAYS be checked
- Press STATUS to check the progress
