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Team:HokkaidoU Japan/Notebook/September8
From 2010.igem.org
(Difference between revisions)
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=Confirmation of pSB1C3= | =Confirmation of pSB1C3= | ||
Because pSB1C3 PCRed from 1-3A（RFP reporter） was used there was posibility of contamination by template which would also produce red colonies. | Because pSB1C3 PCRed from 1-3A（RFP reporter） was used there was posibility of contamination by template which would also produce red colonies. | ||
| - | * H buffer treated 2 uL ＋ Mighty Mix 2 uL ＋ T4 ligase 0.5 | + | * H buffer treated 2 uL ＋ Mighty Mix 2 uL ＋ T4 ligase 0.5 uL → Ligation → [[Team:HokkaidoU_Japan/Protocols|Transformation]] |
* M 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 | ||
| + | * M buffer treated 2 uL → Transformation | ||
=PCR of GFP= | =PCR of GFP= | ||
Latest revision as of 08:14, 27 October 2010
since 13 Jul 2010
since 1 Aug 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 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
- M buffer treated 2 uL → Transformation
