Team:Stockholm/20 September 2010
From 2010.igem.org
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==Andreas== | ==Andreas== | ||
===Assembly of new parts=== | ===Assembly of new parts=== | ||
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*Very weak bands, and in the wrong size... | *Very weak bands, and in the wrong size... | ||
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+ | ==Johan== | ||
+ | |||
+ | * Cut tyrosinase with NgoMIV & SpeI | ||
+ | |||
+ | 10 µl DNA | ||
+ | |||
+ | 2 µl 10x buffer | ||
+ | |||
+ | 1 µl NgoMIV | ||
+ | |||
+ | 1 µl SpeI | ||
+ | |||
+ | 6 µl H2O | ||
+ | |||
+ | * Cut bFGF with BamHI | ||
+ | |||
+ | 2 µl DNA | ||
+ | |||
+ | 2 µl 10x buffer | ||
+ | |||
+ | (1 µl BamHI) | ||
+ | |||
+ | 15 µl H2O | ||
+ | |||
+ | Did a gel and showed that the bFGF are correct | ||
+ | |||
+ | * Ligated tyrosinase into pMA (vector with histag) | ||
+ | |||
+ | 1 µl pMA | ||
+ | |||
+ | 2 µl tyrosinase | ||
+ | |||
+ | 2 µl 10x buffer | ||
+ | |||
+ | 1 µl T4 ligase | ||
+ | |||
+ | 14 µl H2O | ||
+ | |||
+ | {{Stockholm/Footer}} |
Latest revision as of 01:34, 28 October 2010
Contents |
Andreas
Assembly of new parts
- pSB1K3.N-LMWP⋅SOD⋅His
- Dig pSB1C3.N-LMWP (E+A)
- Dig pMA.SOD⋅His (N+P)
- Dig pSB1K3.RFP (E+P)
- pSB1C3.N-LMWP⋅SOD⋅His
- Dig pSB1C3.N-LMWP (A+S)
- Dig pMA.SOD⋅His (N+S)
Digestions
pSB1C3. N-LMWP | pMA. SOD⋅His | pSB1C3. N-LMWP | pSB1K3. N-TAT⋅SOD⋅ His 4 | |
---|---|---|---|---|
10X FastDigest buffer | 3 | 3 | 3 | 2 |
dH2O | 15.2 | 4.1 | 15.2 | 11.4 |
DNA (1 μg) | 9.8 | 20.9 | 9.8 | 4.6 |
AgeI | 1 | 0 | 1 | 0 |
NgoMIV | 0 | 1 | 0 | 0 |
FD SpeI | 1 | 1 | 0 | 0 |
FD EcoRI | 0 | 0 | 1 | 0 |
FD PstI | 0 | 0 | 0 | 1 |
FD XbaI | 0 | 0 | 0 | 1 |
30 μl | 30 μl | 30 μl | 20 μl |
- Incubation: 37 °C, 2:00 (NgoMIV & AgeI); 0:30 (FD)
- Inactivation: 80 °C, 20 min
Gel verification
1.5 % agarose, 120 V
Expected bands
- Dig pSB1C3.N-LMWP A+S 20/9: 2118 bp, (14 bp)
- Dig pMA.SOD⋅His N+S 20/9: 2416 bp, 503 bp
- Dig pSB1C3.N-LMWP E+A 20/9: 2063 bp, 69 bp
- Dig pSB1K3.N-TAT⋅SOD⋅His 4 X+P 20/9: ≈2200 bp, 558 bp
Results
Ligations
- [Dig pSB1K3.RFP E+P 14/9] = 66.6 ng/μl
- [Dig pMA.His⋅SOD E+A 14/9] = 66.6 ng/μl
- [Dig pSB1C3.C-TAT N+P 15/9] = 66.6 ng/μl
- [Dig pSB1C3.N-LMWP A+S 20/9] = 33.3 ng/μl
- [Dig pMA.SOD⋅His N+S 20/9] = 33.3 ng/μl
- [Dig pSB1C3.N-LMWP E+A 20/9] = 33.3 ng/μl
- [Dig pSB1K3.N-TAT⋅SOD⋅His 4 X+P 20/9] = 33.3 ng/μl
pSB1C3. N-LMWP⋅SH | pSB1K3. N-LMWP⋅SH | pSB1A2. RBS.yCCS | pEX. N-TAT⋅SH | |
---|---|---|---|---|
10X T4 Ligase buffer | 2 | 2 | 2 | 2 |
dH2O | 9 | 0 | 11 | 11 |
Vector DNA | 2 | 1.5 | 1.5 | 1.5 |
Insert 1 DNA | 6 | 4.5 | 4.5 | 4.5 |
Insert 2 DNA | – | 11 | – | – |
T4 DNA ligase | 1 | 1 | 1 | 1 |
20 μl | 20 μl | 20 μl | 20 μl |
- Incubation: 22 °C, 15 min
Transformations
Standard transformations, procedures according to protocol.
- 1 μl ligation mix
- Lig pSB1C3.N-LMWP⋅SH (Cm 25)
- Lig pSB1K3.N-LMWP⋅SH (Km 50)
- Lig pSB1A2.RBS.yCCS (Amp 100)
- Lig pEX.N-TAT⋅SH (Amp 100 + 50 μl 0.1 mM IPTG)
Mimmi
his.SOD.cTAT
Gel
well | sample |
---|---|
1 | ladder |
2 | pSB1C3.his.SOD.cTAT 1 |
3 | pSB1C3.his.SOD.cTAT 2 |
4 | pSB1C3.his.SOD.cTAT 3 |
5 | pSB1C3.his.SOD.cTAT 4 |
6 | pSB1C3.his.SOD.cTAT 5 |
7 | pSB1C3.his.SOD.cTAT 6 |
8 | pSB1C3.his.SOD |
9 | pEX.SOD |
PhastGel
well | sample | |
---|---|---|
1 | SOD.his 0h | |
2 | SOD.his 2h 1:1.5 | |
3 | his.SOD 0h | |
4 | his.SOD 2h 1:2 | |
5 | yCCS 1 2h 1:2 | |
6 | ladder |
pEX.SOD.his
Gel
well | sample |
---|---|
1 | ladder |
2 | pEX.SOD.his |
3 | pEX.his.SOD |
4 | yCCS 1 |
5 | yCCS 2 |
- Very weak bands, and in the wrong size...
Johan
- Cut tyrosinase with NgoMIV & SpeI
10 µl DNA
2 µl 10x buffer
1 µl NgoMIV
1 µl SpeI
6 µl H2O
- Cut bFGF with BamHI
2 µl DNA
2 µl 10x buffer
(1 µl BamHI)
15 µl H2O
Did a gel and showed that the bFGF are correct
- Ligated tyrosinase into pMA (vector with histag)
1 µl pMA
2 µl tyrosinase
2 µl 10x buffer
1 µl T4 ligase
14 µl H2O
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