August/21 August 2009
From 2009.igem.org
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Latest revision as of 08:01, 12 October 2009
transformation
to get new plasmid
- ⑤(RBS+rhlR+terminator+promoter(reg))
- ⑦(RBS+cinR)
- ⑧(RBS+luxI)
check the result of transformation
Checked the cell cultures transformed and plated out yesterday (8/10) for colony formation and made an approximate count of the number of colonies.
(plate number)-(location on plate) (no. of colonies)
[http://partsregistry.org/wiki/index.php?title=Part:BBa_C0170 2-8G] 4 [http://partsregistry.org/wiki/index.php?title=Part:BBa_F2621 2-21F] 0 [http://partsregistry.org/wiki/index.php?title=Part:BBa_I13521 2-6O] 2 [http://partsregistry.org/wiki/index.php?title=Part:BBa_E2050 2-13N] <15 ⑤ 0
restriction and digestion
K204009
Vector | Insert | ||
---|---|---|---|
terminater([http://partsregistry.org/wiki/index.php?title=Part:BBa_B0015 1-23L]) | 10 | ①-3(RBS+LasR) | 12 |
EcoRI | 1 | EcoRI | 1 |
XbaI | 1 | SpeI | 1 |
No.2 | 2 | No.2 | 2 |
dH2O | 4 | dH2O | 4 |
total | 20uL | total | 20uL |
K204010
Vector | Insert | ||
---|---|---|---|
RBS([http://partsregistry.org/wiki/index.php?title=Part:BBa_B0034 1-2M]) | 10 | EpsE+terminater(②-A) | 12 |
SpeI | 1 | XbaI | 1 |
PstI | 1 | PstI | 1 |
No.2 | 2 | No.2 | 2 |
dH2O | 6 | dH2O | 4 |
total | 20uL | total | 20uL |
K204011
Vector | Insert | ||
---|---|---|---|
p(tetR)([http://partsregistry.org/wiki/index.php?title=Part:BBa_R0040 1-6I]) | 10 | RBS+GYP+terminater([http://partsregistry.org/wiki/index.php?title=Part:BBa_E0240 1-12M]) | 12 |
SpeI | 1 | XbaI | 1 |
PstI | 1 | PstI | 1 |
No.2 | 2 | No.2 | 2 |
dH2O | 6 | dH2O | 4 |
total | 20uL | total | 20uL |
↓
37°C, 2hr
↓
gel electrophoresis
gel cut
'8/22
purification by [QIAquick Nucleotide Removal Kit]
↓
ligation
ligation DNA 44 10* buffer 5 ligation 1 total 50uL ↓ 16°C , 4hr