Team:EPF-Lausanne/Protocols/TetR

From 2011.igem.org

(Difference between revisions)
(Materials)
(Protocol)
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== Protocol ==
== Protocol ==
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== PCR Cycle ==
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* Put mix in PCR thermal cycler
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<b>1.</b> 98°C for 30s
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* Program the PCR thermal cycler: <b>1.</b> 98°C for 30s <b>2.</b> 98°C for 7.5 seconds <b>3.</b> 58°C for 20 sec (this depends on the primers, therefore look up the annealing temperature of the primers used) <b>4.</b> 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) <b>6.</b> 72°C for 5 min <b>7.</b> 4°C "forever"
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<b>2.</b> 98°C for 7.5 seconds
 +
<b>3.</b> 58°C for 20 sec (this depends on the primers, therefore look up the annealing temperature of the primers used)
 +
<b>4.</b> 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)  
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<b>5.</b> 72°C for 5 min
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<b>6.</b> 4°C "forever"
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*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
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*Press STATUS to check the progress
*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
*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
*Press STATUS to check the progress

Revision as of 12:21, 7 July 2011