August/21 August 2009

From 2009.igem.org

(Difference between revisions)
Line 64: Line 64:
gel electrophoresis<br>
gel electrophoresis<br>
gel cut<br>
gel cut<br>
 +
<br>
 +
<br>
 +
 +
8/22<br>
 +
purification by [QIAquick Nucleotide Removal Kit]<br>
 +
↓<br>
 +
ligation
 +
ligation
 +
DNA        44
 +
10* buffer 5
 +
ligation  1
 +
total      50uL
 +
 +
16°C overnight

Revision as of 05:45, 22 August 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)
2-8G 4 2-21F 0 2-6O 2 2-13N <15 ⑤ 0


restriction and digestion

K204009

VectorInsert
terminater(1-23L)10①-3(RBS+LasR)12
EcoRI1EcoRI1
XbaI1SpeI1
No.22No.22
dH2O4dH2O4
total20uLtotal20uL


K204010

VectorInsert
RBS(1-2M)10EpsE+terminater(②-A)12
SpeI1XbaI1
PstI1PstI1
No.2 2No.22
dH2O6dH2O4
total20uLtotal20uL


K204011

VectorInsert
p(tetR)(1-6I)10RBS+GYP+terminater(1-12M)12
SpeI1XbaI1
PstI1PstI1
No.2 2No.22
dH2O6dH2O4
total20uLtotal20uL



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 overnight