Team:KAIT Japan/Notebook
From 2012.igem.org
Project | Parts | Notebook |
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During the creation.
Contents |
Creating parts of Tar methylation region.
Date:8/9
Colony PCR
Reagent
- TaKaRa Ex Taq(5units/μL) 0.5μL
- 10×Ex Taq buffer 10μL
- dNTP Mixture(2.5Meach) 8μL
- Primer F(10μM) 4μL
- Primer R(10μM) 4μL
- Template(E.coli DH5α)
→Reflection:We Took E.coli too many.You should take less E.coli.
Conditions of the thermal cycler
- 95°C(5min)
- 94°C(30sec)
- 61°C(30sec)
- 71°C(40sec)
- 72°C(1min)
- 4°C(Save)
- 2~4:35cycle→Reflection:The number of cycles was less.So,We increased The number of cycles in 8/11.(50 cycles)
Date:8/11
The purified DNA
- Electrophoresis
- Marker:pigment(buffer) 1μL,DNA molecule 2μL,TE buffer 3μL
- Sample:pigment(buffer) 1μL,sample 5μL
- Gel concentration:1.2%,Migration time:30min
→Reflection:Band was less.
- Storage
PCR Product
- Electrophoresis
- The gel check and cut
- DNA purification
- Confirmation of electrophoresis
- PCR
- 50cycle
- Storage
Date:8/13
Confirmed of electrophoresis by PCR product and Ligation of the TA vector
- Electrophoresis
- Gel concentration:1.2%,Migration time:30min
- Marker:Flash Gel 5μL
- Sample:pigment 1μL,sample 5μL
- Check and Colony PCR
- Add to TA vector
- PCR product 2μL
- pMD20-Tvector 1μL
- D2W 2μL
- Ligation Mighty Mix 5μL
- Heat insulation(16°C,30min)
- Storage(-20°C)
Date:8/14
Transformation
- Put competent cells on ice(10~15min)
- Add Ligation reaction solution(10μL) and tapping
- On the ice(30min)[Transformation]
- Add LB medium(0.7mL)
- Incubate(60min,37°C)
- Add X-gal(40μL) and ampicillin(10μL)[200μg/mL] on LB agar medium(IPTG)
- Add one incubated(100μL)
- Cultivation(overnight)