Team:HokkaidoU Japan/Notebook/aggregation Week 6
From 2012.igem.org
(Difference between revisions)
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</p> | </p> | ||
+ | ==mini-prep== | ||
+ | <p> | ||
+ | mini-prep of pBad-RBS. We used FastGene Plasmid Mini Kit(Nippon Genetics) and got 50 ul of DNA solutions. | ||
+ | [[image:|thumb|mini-prep result]] | ||
+ | </p> | ||
+ | |||
+ | ==transformation== | ||
+ | <p> | ||
+ | Transformation of plasmid DNA (pT7-RBS-Ag43-dT on pSB1K3) in E. coli(DH5α). | ||
+ | #Added 2 ul of plasmid DNA to 50 ul of thawed competent cells on ice. | ||
+ | #Incubated on ice for 30 min. | ||
+ | #Added 600 ul of LB then incubated the cells for 2 hours at 37C. | ||
+ | #Prepared and Labeled two LBK plates. | ||
+ | #Plated 300 ul of the culture onto first dish and spread. | ||
+ | #Added 900 ul of LB to 100 ul of the culture and plated 300 ul of it onto second dish and spread. | ||
+ | #Incubated them at 37C for hours. | ||
+ | |||
+ | </p> | ||
</div><div> | </div><div> | ||
Revision as of 07:52, 6 August 2012
Contents |
August 6th
Ethanol precipitation
Ethanol precipitation for digestion and gel extraction product.
- Added 5 ul of NaoAc, 1.5 ul of glycogen and 125ul of 100% ethanol.
- Centrifuged in 15000 rpm, 10 min at 4C.
- Remove supernatant and added 220ul of 70% ethanol.
- Centrifuged in 15000 rpm, 10 min at 4C.
- Remove supernatant and air drying in room temperature then added 10 ul of DW.
Ligation
We ligated pT7-RBS on pSB1K3 (digested Spe1) as vector and Ag43-dT (digested Spe1 and Xba1 and HindIII) as insert.
pT7-RBS | 1 ul |
Ag43-dT | 2 ul |
DW | 2 ul |
Ligation Mighty Mix(TAKARA) | 5 ul |
Total | 10 ul |
Ligation reaction time was written below.
Degree | Minute |
16 | 30 |
65 | 10 |
4 | Hold |
mini-prep
mini-prep of pBad-RBS. We used FastGene Plasmid Mini Kit(Nippon Genetics) and got 50 ul of DNA solutions. [[image:|thumb|mini-prep result]]
transformation
Transformation of plasmid DNA (pT7-RBS-Ag43-dT on pSB1K3) in E. coli(DH5α).
- Added 2 ul of plasmid DNA to 50 ul of thawed competent cells on ice.
- Incubated on ice for 30 min.
- Added 600 ul of LB then incubated the cells for 2 hours at 37C.
- Prepared and Labeled two LBK plates.
- Plated 300 ul of the culture onto first dish and spread.
- Added 900 ul of LB to 100 ul of the culture and plated 300 ul of it onto second dish and spread.
- Incubated them at 37C for hours.