Team:EPF-Lausanne/Protocols/TetR
From 2011.igem.org
(Difference between revisions)
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- | == Gene PCR == | + | == <b>Gene PCR</b> == |
== Materials == | == Materials == | ||
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*36.5 µl H2O | *36.5 µl H2O | ||
- | + | == PCR Cycle (30 cycles) == | |
- | == PCR Cycle == | + | |
<b>1.</b> 98°C for 30s | <b>1.</b> 98°C for 30s | ||
<b>2.</b> 98°C for 7.5 seconds | <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>3.</b> 58°C for 20 sec (this depends on the primers, |
- | <b>4.</b> 72°C for 15 sec; you have to calculate the time required. This polymerase has an effciency of 15-30s/kb. | + | 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>5.</b> 72°C for 5 min | <b>5.</b> 72°C for 5 min | ||
<b>6.</b> 4°C "forever" | <b>6.</b> 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 | *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 | ||
+ | |||
+ | == <b>Extension PCR</b> == | ||
+ | |||
+ | == Materials == | ||
+ | |||
+ | * Gene PCR product | ||
+ | * Extension primers 500nM | ||
+ | |||
+ | == PCR Cycle (30 cycles) == | ||
+ | |||
+ | <b>1.</b> 98°C for 30s | ||
+ | <b>2.</b> 98°C for 7.5 seconds | ||
+ | <b>3.</b> 58°C for 20 sec | ||
+ | <b>4.</b> 72°C for 15 sec; | ||
+ | (calculate for the longest fragment) | ||
+ | <b>5.</b> 72°C for 5 min | ||
+ | <b>6.</b> 4°C "forever" | ||
+ | |||
+ | |||
+ | == Materials == | ||
+ | |||
+ | * 1µl Final primers | ||
+ | |||
+ | == PCR Cycle (10 cycles) == | ||
+ | |||
+ | <b>1.</b> 98°C for 30s | ||
+ | <b>2.</b> 98°C for 7.5 seconds | ||
+ | <b>3.</b> 58°C for 20 sec | ||
+ | <b>4.</b> 72°C for 15 sec; <b>5.</b> 72°C for 5 min | ||
+ | <b>6.</b> 4°C "forever" | ||
{{:Team:EPF-Lausanne/Templates/Footer}} | {{:Team:EPF-Lausanne/Templates/Footer}} |
Revision as of 14:17, 7 July 2011
Linear template- TetR
Two step extension PCR
Contents |
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
PCR Cycle (30 cycles)
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)
5. 72°C for 5 min 6. 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
Extension PCR
Materials
- Gene PCR product
- Extension primers 500nM
PCR Cycle (30 cycles)
1. 98°C for 30s 2. 98°C for 7.5 seconds 3. 58°C for 20 sec 4. 72°C for 15 sec; (calculate for the longest fragment) 5. 72°C for 5 min 6. 4°C "forever"
Materials
- 1µl Final primers
PCR Cycle (10 cycles)
1. 98°C for 30s 2. 98°C for 7.5 seconds 3. 58°C for 20 sec 4. 72°C for 15 sec; 5. 72°C for 5 min 6. 4°C "forever"