Team:Bielefeld-Germany/Labjournal/Molecular
From 2013.igem.org
Genetic enginering protocols
For the isolation following kit has been used: Fermentas GeneJET™ Plasmid Miniprep Kit
- Centrifuge 10 mL of over-night liquid culture
- Resuspend pellet in 800 µL of resuspension solution
- Ribolyse three times for 60 s with 6500 rpm (30 s break between every run, 400 mg beads)
- Centrifuge 3 min at 10,000 rpm
- Transfer 500 µL of supernatant into new 2 mL tube
- Add 500 µL of lysis buffer, invert 4 - 6 times
- Add 700 µL of neutralisation buffer, invert 4 - 6 times
- Centrifuge 10 min at 12,000 rpm
- Transfer 2 x 600 µL of supernatant into spin column (centrifuge down each time for 30 s at 12,000 rpm)
- Two wash steps with 750 µL of washing buffer
- Dry column
- Elute in 75 µL of elution buffer
-
-
-
-
Specific Protocols
Reagent | 1x | 8x |
---|---|---|
Hf-Buffer 5x | 10.0 | 88.0 |
dNTPs (10mM) | 2.0 | 17.6 |
Primer1 (10mM) | 1.0 | 8.8 |
Primer2 (10mM) | 1.0 | 8.8 |
Template (16.5ng) | 3.0 | 26.4 |
DMSO | 4.0 | 35.2 |
Phusion (0.5u) | 1.0 | 8.8 |
H2O | 26.0 | 228.8 |
Program Phusion | ||||
---|---|---|---|---|
98 °C | 98 °C | 68 °C | 72 °C | 72 °C |
30s | 10s | 30s | 1:35 | 6:00 |
35 cycles | ||||
Notes:
Size: 1800bp Primer1: Primer2: |
Reagent | 1x | 8x |
---|---|---|
Hf-Buffer 5x | 10.0 | 88.0 |
dNTPs (10mM) | 2.5 | 22.0 |
Primer1 (10mM) | 1.0 | 8.8 |
Primer2 (10mM) | 1.0 | 8.8 |
Template (5.5ng/ul) | 2.0 | 17.6 |
DMSO | 3.0 | 26.4 |
Phusion (0.5u) | 1.0 | 8.8 |
H2O | 29.5 | 259.6 |
Program Phusion | ||||
---|---|---|---|---|
98 °C | 98 °C | 60 °C | 72 °C | 72 °C |
1:00 | 10s | 30s | 30s | 6:00 |
35 cycles | ||||
Notes:
Size: 330bp Primer1: Primer2: |