Team:HokkaidoU Japan/Notebook/September8
From 2010.igem.org
(Difference between revisions)
(→pSB1C3の確認) |
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* H buffer treated 2 uL → Transformation | * H buffer treated 2 uL → Transformation | ||
- | = | + | =PCR of GFP= |
* GFP reporter BBa_I13522 pSB1A2 2-8A 937bp | * GFP reporter BBa_I13522 pSB1A2 2-8A 937bp | ||
* GFP protein BBa_E0840 pSB1A2 1-12O 878bp | * GFP protein BBa_E0840 pSB1A2 1-12O 878bp | ||
- | + | PCR cocktai was same as September 1st`s |
Revision as of 18:01, 27 September 2010
Colony PCR
Checked if primers PS-R, EX-F were good to use for colony PCR and also checked if insert was realy in plasmids
- September 6th transformation (digestion was done with H buffer×2 and M buffer×2, 2 version)
- 1-3A
- Retried September 6th transformation
- pUC119
Confirmation of pSB1C3
Because pSB1C3 PCRed from 1-3A(RFP reporter) was used there was posibility of contamination tion by template which would also produce red colonies.
- H buffer treated 2 uL + Mighty Mix 2 uL + T4 ligase 0.5 uL → Ligation → Transformation
- M buffer treated 2 uL + Mighty Mix 2 uL + T4 ligase 0.5 uL → Ligation → Transformation
- H buffer treated 2 uL → Transformation
- H buffer treated 2 uL → Transformation
PCR of GFP
- GFP reporter BBa_I13522 pSB1A2 2-8A 937bp
- GFP protein BBa_E0840 pSB1A2 1-12O 878bp