Team:Stockholm/5 September 2010
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(New page: {{Stockholm/Top2}} == Mimmi == === MITF-M === ==== Gel ==== {| ! well ! sample |- | 1 | 1kb ladder |- | 2 | MITF-M 1 |- | 3 | MITF-M 2 |- | 4 | MITF-M 3 |- | 5 | MITF-M 4 |- | 6 | bla...)
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(New page: {{Stockholm/Top2}} == Mimmi == === MITF-M === ==== Gel ==== {| ! well ! sample |- | 1 | 1kb ladder |- | 2 | MITF-M 1 |- | 3 | MITF-M 2 |- | 4 | MITF-M 3 |- | 5 | MITF-M 4 |- | 6 | bla...)
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Revision as of 14:04, 6 September 2010
Contents |
Mimmi
MITF-M
Gel
well | sample |
---|---|
1 | 1kb ladder |
2 | MITF-M 1 |
3 | MITF-M 2 |
4 | MITF-M 3 |
5 | MITF-M 4 |
6 | blank |
- nothing...
- Make a new colony PCR with DreamTaq
SOD.his/his.SOD
- Weigh the gel slices and add XP2
tube | gel+tube | gel | XP2 | tot | |
---|---|---|---|---|---|
SOD.his | 0.99g | 1.45g | 0.46g | 460µl | 920µl |
his.SOD | 0.99g | 1.37g | 0.38g | 380µl | 760µl |
- Incubate at 60°C for 7m or until the gel has melted
- Follow the E.Z.N.A. gel extraction kit
- Wash 2 times with SPW wash buffer
- Incubate 1m and then eluate with 50µl dH2O
- DNA conc.
- not able to measure...
Ligation
pSB1C3 | pEX | Conditions | ||||
---|---|---|---|---|---|---|
Mix | (µl) x2 | (µl) x2 | time | °C | ||
vector | 1 | 2 | 10m | 22 | ||
DNA | 14 | 13 | ||||
5x buffer | 4 | 4 | ||||
T4 ligase | 1 | 1 | ||||
sH2O | 0 | 0 | ||||
tot | 20µl | 20µl |
MITF-M
Colony PCR
Mix | (µl) | x6 | Primers | conditions | ||||
---|---|---|---|---|---|---|---|---|
sH2O | 17.25 | 103.5 | pSB_VF2 | time | °C | |||
dNTP | 2.5 | 15 | pSB_VR | 2m | 95 | |||
F primer | 1 | 6 | 30s | 95 | ) | |||
R primer | 1 | 6 | 30s | 55 | > 30 cycles | |||
10x buffer | 2.5 | 15 | 1m20s | 72 | ) | |||
DreamTaq | 0.25 | 1.5 | 10m | 72 | ||||
DNA | 0.5 | 6x0.5 | oo | 10 | ||||
tot | 25µl | 150µl |