Team:HokkaidoU Japan/Notebook/September3
From 2010.igem.org
Resultsof yesterdays trnsformation
- pSB1C3 uterly failed to produce colonies
- pUC119 produced 20 colonies
- colonies that should been red because of RFP insert wasn`t, so there is posibility that insert wasn`t there
Colony PCR on yesterdays E.coli
- Colony PCR was done acordig to protocol
- This day we did 20 samples
Electrophoresis
Concentration check of parts used for transformation yesterday
Confirmed that DNA solution concentration of parts for Ligation was as anticipated (good?)
Lane | DNA |
1 | |
2 | Lambda/Hind III, EcoR I |
3 | |
4 | RFP |
5 | pUC119 |
6 | pSB1C3 |
1-3AのPCR
1-3AはpSB1C3に載ったRFP reporterで,トラフォメに成功している
ベクターとして配布されたpSB1C3が悪い可能性を見るため,このパーツのpSB1C3を増幅して使用する
Reagent | Amount |
---|---|
1-3A | 1 |
DW | 33 |
10x Buffer | 5 |
2 M 4dNTPs | 5 |
25 mM MgSO4 | 3 |
Suffix-F | 1 |
Prefix-R | 1 |
KOD | 1 |
Total | 50 uL |
- extensionは120 sec
- YM-10でClean Upしたら43 uLになった